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<!--
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UID=57729
|
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ConceptID=C0151683
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Neutrophilia</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>57729</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0151683</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Increased neutrophils</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Neutrophilia (165518003); Neutrophilic leukocytosis (165518003); Neutrophil count above reference range (165518003)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0011897">HP:0011897</a></td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">Increased number of neutrophils circulating in blood. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Neutrophilia</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/1702861" ref="tree=MeSH" title="MedGen record for Abnormal immune system morphology">Abnormal immune system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/869190" ref="tree=MeSH" title="MedGen record for Abnormal cellular immune system morphology">Abnormal cellular immune system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/508852" ref="tree=MeSH" title="MedGen record for Abnormal leukocyte morphology">Abnormal leukocyte morphology</a></span><ul><li><span class="TLline"><a href="/medgen/488926" ref="tree=MeSH" title="MedGen record for Abnormal leukocyte count">Abnormal leukocyte count</a></span><ul><li><span class="TLline"><a href="/medgen/1704843" ref="tree=MeSH" title="MedGen record for Abnormal granulocyte count">Abnormal granulocyte count</a></span><ul><li><span class="TLline"><a href="/medgen/663207" ref="tree=MeSH" title="MedGen record for Abnormal neutrophil count">Abnormal neutrophil count</a></span><ul><li><span class="matched_ds">Neutrophilia</span><ul><li><span class="TLline"><a href="/medgen/1693276" ref="tree=MeSH" title="MedGen record for Neutrophilia in absence of infection">Neutrophilia in absence of infection</a></span></li><li><span class="TLline"><a href="/medgen/1707092" ref="tree=MeSH" title="MedGen record for Neutrophilia in presence of infection">Neutrophilia in presence of infection</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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</div>
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||
<div class="portlet mgSection" id="ID_112">
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||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln clinfeat">
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||
<div class="divPopper rprt" id="rdis_45811"><div><strong>Familial Mediterranean fever</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>45811</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0031069</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Familial Mediterranean fever (FMF) is divided into two phenotypes: type 1 and type 2. FMF type 1 is characterized by recurrent short episodes of inflammation and serositis including fever, peritonitis, synovitis, pleuritis, and, rarely, pericarditis and meningitis. The symptoms and severity vary among affected individuals, sometimes even among members of the same family. Amyloidosis, which can lead to kidney failure, is the most severe complication, if untreated. FMF type 2 is characterized by amyloidosis as the first clinical manifestation of FMF in an otherwise asymptomatic individual.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/45811">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_581114"><div><strong>Acrodermatitis continua suppurativa of Hallopeau</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>581114</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0392439</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare, genetic, chronic, recurrent, slowly progressive, epidermal disease characterized by small, sterile, pustular eruptions, involving the nails and surrounding skin of the fingers and/or toes, which coalesce and burst, leaving erythematous, atrophic skin where new pustules develop. Onychodystrophy is frequently associated and anonychia and osteolysis are reported in severe cases. Local expansion (to involve the hands, forearms and/or feet) and involvement of mucosal surfaces (e.g. conjunctiva, tongue, urethra) may be observed.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/581114">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_140768"><div><strong>Hyperimmunoglobulin D with periodic fever</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>140768</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0398691</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Mevalonate kinase deficiency is a condition characterized by recurrent episodes of fever, which typically begin during infancy. Each episode of fever lasts about 3 to 6 days, and the frequency of the episodes varies among affected individuals. In childhood the fevers seem to be more frequent, occurring as often as 25 times a year, but as the individual gets older the episodes occur less often.\n\nMevalonate kinase deficiency has additional signs and symptoms, and the severity depends on the type of the condition. There are two types of mevalonate kinase deficiency: a less severe type called hyperimmunoglobulinemia D syndrome (HIDS) and a more severe type called mevalonic aciduria (MVA).\n\nPeople with MVA have signs and symptoms of the condition at all times, not just during episodes of fever. Affected children have developmental delay, problems with movement and balance (ataxia), recurrent seizures (epilepsy), progressive problems with vision, and failure to gain weight and grow at the expected rate (failure to thrive). Individuals with MVA typically have an unusually small, elongated head. In childhood or adolescence, affected individuals may develop eye problems such as inflammation of the eye (uveitis), a blue tint in the white part of the eye (blue sclera), an eye disorder called retinitis pigmentosa that causes vision loss, or clouding of the lens of the eye (cataracts). Affected adults may have short stature and may develop muscle weakness (myopathy) later in life. During fever episodes, people with MVA may have an enlarged liver and spleen (hepatosplenomegaly), lymphadenopathy, abdominal pain, diarrhea, and skin rashes. Children with MVA who are severely affected with multiple problems may live only into early childhood; mildly affected individuals may have a normal life expectancy.\n\nDuring episodes of fever, people with HIDS typically have enlargement of the lymph nodes (lymphadenopathy), abdominal pain, joint pain, diarrhea, skin rashes, and headache. Occasionally they will have painful sores called aphthous ulcers around their mouth. In females, these may also occur around the vagina. Rarely, people with HIDS develop a buildup of protein deposits (amyloidosis) in the kidneys that can lead to kidney failure. Fever episodes in individuals with HIDS can be triggered by vaccinations, surgery, injury, or stress. Most people with HIDS have abnormally high levels of immune system proteins called immunoglobulin D (IgD) and immunoglobulin A (IgA) in the blood. It is unclear why some people with HIDS have high levels of IgD and IgA and some do not. Elevated levels of these immunoglobulins do not appear to cause any signs or symptoms. Individuals with HIDS do not have any signs and symptoms of the condition between fever episodes and typically have a normal life expectancy.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/140768">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_96022"><div><strong>Leukocyte adhesion deficiency type II</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>96022</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0398739</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Congenital disorder of glycosylation type IIc (CDG2C) is an autosomal recessive disorder characterized by moderate to severe psychomotor retardation, mild dysmorphism, and impaired neutrophil motility. It is a member of a group of disorders with a defect in the processing of protein-bound glycans. For a general overview of congenital disorders of glycosylation (CDGs), see CDG1A (212065) and CDG2A (212066). Frydman (1996) contended that the neutrophil defect in CDG2C, which has been referred to as 'leukocyte adhesion deficiency type II' (LAD2), is a manifestation of the disorder and that there are no cases of 'primary' LAD II. Etzioni and Harlan (1999) provided a comprehensive review of both leukocyte adhesion deficiency-1 (LAD1; 116920) and LAD2. While the functional neutrophil studies are similar in the 2 LADs, the clinical course is milder in LAD2. Furthermore, patients with LAD2 present other abnormal features, such as growth and mental retardation, which are related to the primary defect in fucose metabolism. Delayed separation of the umbilical cord occurs in LAD1. For a discussion of genetic heterogeneity of LAD, see 116920.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/96022">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_154252"><div><strong>Hereditary neutrophilia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>154252</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0543669</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare, genetic, immune disease characterized by chronic neutrophilia, increase in the percentage of circulating CD34+ cells in peripheral blood, increase in granulocyte precursors in bone marrow and splenomegaly. Patients are predominantly asymptomatic, but may present with systemic inflammatory response syndrome with fever, dyspnea, tachycardia, pleural and pericardial effusion, or myelodysplastic syndrome.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/154252">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_374920"><div><strong>Neutrophil immunodeficiency syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>374920</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1842398</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Immunodeficiency-73A with defective neutrophil chemotaxis and leukocytosis (IMD73A) is an immunologic disorder characterized by onset of recurrent infections in early infancy. Affected infants have periumbilical erythema and later develop skin abscesses and invasive infections. Laboratory studies show leukocytosis, neutrophilia, decreased TRECs, and T-cell abnormalities. Neutrophils showed decreased chemotaxis associated with actin polymerization abnormalities, as well as variably impaired oxidative responses. Hematopoietic stem cell transplant may be curative (summary by Accetta et al., 2011; review by Lougaris et al., 2020). In a review of autosomal forms of chronic granulomatous disease (see 306400 for genetic heterogeneity of CGD), Roos et al. (2021) noted that patients with RAC2 mutations may manifest CGD-like symptoms due to defects in neutrophil NADPH oxidase activity.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/374920">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_411230"><div><strong>Sterile multifocal osteomyelitis with periostitis and pustulosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>411230</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C2748507</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Chronic recurrent multifocal osteomyelitis-2 with periostitis and pustulosis (CRMO2) is an autosomal recessive multisystemic autoinflammatory disorder characterized by onset of symptoms in early infancy. Affected individuals present with joint swelling and pain, pustular rash, oral mucosal lesions, and fetal distress. The disorder progresses in severity to generalized severe pustulosis or ichthyosiform lesions and diffuse bone lesions. Radiographic studies show widening of the anterior rib ends, periosteal elevation along multiple long bones, multifocal osteolytic lesions, heterotopic ossification, and metaphyseal erosions of the long bones. Laboratory studies show elevation of inflammatory markers. The disorder results from unopposed activation of the IL1 inflammatory signaling pathway. Treatment with the interleukin-1 receptor antagonist anakinra may result in clinical improvement (Aksentijevich et al., 2009). For a discussion of genetic heterogeneity of CRMO, see 609628.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/411230">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_865178"><div><strong>Immunodeficiency 32B</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>865178</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4016741</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Immunodeficiency-32B is an autosomal recessive primary immunodeficiency characterized by recurrent infections resulting from variable defects in immune cell development or function, including monocytes, dendritic cells, and natural killer (NK) cells. Patients have particular susceptibility to viral disease (summary by Mace et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/865178">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934581"><div><strong>Autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934581</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4310614</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive autoinflammation, panniculitis, and dermatosis syndrome (AIPDSB) is an autoinflammatory disease characterized by neonatal onset of recurrent fever, erythematous rash with painful nodules, painful joints, and lipodystrophy. Additional features may include diarrhea, increased serum C-reactive protein (CRP; 123260), leukocytosis, and neutrophilia in the absence of any infection. Patients exhibit no overt primary immunodeficiency (Damgaard et al., 2016 and Zhou et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934581">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1612104"><div><strong>Immunodeficiency 53</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1612104</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4539811</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1612104">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1787468"><div><strong>Immunodeficiency 14b, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1787468</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5543301</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive primary immunodeficiency-14B (IMD14B) is characterized by onset of recurrent infections in early childhood. Most patients have respiratory infections, but some may develop inflammatory bowel disease or osteomyelitis. Laboratory studies tend to show hypogammaglobulinemia and decreased levels of B cells. Although NK cell and T cell numbers are normal, there may be evidence of impaired immune-mediated cytotoxicity and defective T-cell function (summary by et al., 2018 and et al., 2019).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1787468">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794283"><div><strong>Immunodeficiency 91 and hyperinflammation</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794283</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5562073</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Immunodeficiency-91 and hyperinflammation (IMD91) is an autosomal recessive complex immunologic disorder characterized by both immunodeficiency and recurrent infections, often to viruses or mycobacteria, as well as by hyperinflammation with systemic involvement. Affected individuals present in infancy with variable features, including fever, infection, thrombocytopenia, renal or hepatic dysfunction, recurrent infections, or seizures. Most patients eventually develop hepatic or renal failure, compromised neurologic function, lymphadenopathy or hepatosplenomegaly, and multiorgan failure resulting in death. More variable features may include intermittent monocytosis, features of hemophagocytic lymphohistiocytosis (HLH), and serologic evidence of hyperinflammation. The disorder is thought to result from dysregulation of the interferon response to viral stimulation in the innate immune system (summary by Le Voyer et al., 2021; Vavassori et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794283">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1851770"><div><strong>Immunodeficiency 113 with autoimmunity and autoinflammation</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1851770</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5882711</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Immunodeficiency-113 with autoimmunity and autoinflammation (IMD113) is an autosomal recessive complex immunologic disorder with onset of symptoms in infancy. Affected individuals have recurrent infections and usually show features of autoimmunity and autoinflammation, such as hemolytic anemia, thrombocytopenia, hepatosplenomegaly, leukocytosis, neutrophilia, and elevated acute phase reactants. More variable systemic features may include celiac disease or enteropathy, ileus, nephropathy, eczema, and dermatomyositis. Additional features include facial dysmorphism, scoliosis, and poor wound healing. One patient with neurodevelopmental abnormalities has been reported. The disorder results from dysregulation of the actin cytoskeleton that affects certain cell lineages (Nunes-Santos et al., 2023).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1851770">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_581114" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acrodermatitis continua suppurativa of Hallopeau</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934581" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessive</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_45811" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Familial Mediterranean fever</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_154252" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hereditary neutrophilia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_140768" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hyperimmunoglobulin D with periodic fever</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (13)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1851770" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency 113 with autoimmunity and autoinflammation</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1787468" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency 14b, autosomal recessive</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_865178" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency 32B</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1612104" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency 53</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794283" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency 91 and hyperinflammation</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_96022" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Leukocyte adhesion deficiency type II</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_374920" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neutrophil immunodeficiency syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_411230" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Sterile multifocal osteomyelitis with periostitis and pustulosis</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38066919">Atypical CML: diagnosis and treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Breccia M</span><br />
|
||
<span class="medgenPMjournal">Hematology Am Soc Hematol Educ Program</span>
|
||
2023 Dec 8;2023(1):476-482.
|
||
doi: 10.1182/hematology.2023000448.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38066919" target="_blank">38066919</a><a href="/pmc/articles/PMC10727105" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36601682">Atypical chronic myeloid leukemia and myelodysplastic/myeloproliferative neoplasm, not otherwise specified: 2023 update on diagnosis, risk stratification, and management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Patnaik MM,
|
||
Tefferi A</span><br />
|
||
<span class="medgenPMjournal">Am J Hematol</span>
|
||
2023 Apr;98(4):681-689.
|
||
Epub 2023 Jan 4
|
||
doi: 10.1002/ajh.26828.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36601682" target="_blank">36601682</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28439845">A Systematic Review of the Clinical Presentation, Diagnosis, and Treatment of Small Bowel Obstruction.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rami Reddy SR,
|
||
Cappell MS</span><br />
|
||
<span class="medgenPMjournal">Curr Gastroenterol Rep</span>
|
||
2017 Jun;19(6):28.
|
||
doi: 10.1007/s11894-017-0566-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28439845" target="_blank">28439845</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22neutrophilia%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (70)</a></div></div>
|
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</div>
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||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
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to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
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<div class="portlet mgSection" id="ID_103">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38066919">Atypical CML: diagnosis and treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Breccia M</span><br />
|
||
<span class="medgenPMjournal">Hematology Am Soc Hematol Educ Program</span>
|
||
2023 Dec 8;2023(1):476-482.
|
||
doi: 10.1182/hematology.2023000448.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38066919" target="_blank">38066919</a><a href="/pmc/articles/PMC10727105" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37943073">Hepatic abscessation in dogs: A multicenter study of 56 cases (2010-2019).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Burke JE,
|
||
Hess RS,
|
||
McEntee EP,
|
||
Griffin MA,
|
||
Harmon SM,
|
||
Silverstein DC</span><br />
|
||
<span class="medgenPMjournal">J Vet Emerg Crit Care (San Antonio)</span>
|
||
2023 Nov-Dec;33(6):665-675.
|
||
Epub 2023 Nov 9
|
||
doi: 10.1111/vec.13340.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37943073" target="_blank">37943073</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36601682">Atypical chronic myeloid leukemia and myelodysplastic/myeloproliferative neoplasm, not otherwise specified: 2023 update on diagnosis, risk stratification, and management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Patnaik MM,
|
||
Tefferi A</span><br />
|
||
<span class="medgenPMjournal">Am J Hematol</span>
|
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2023 Apr;98(4):681-689.
|
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Epub 2023 Jan 4
|
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doi: 10.1002/ajh.26828.
|
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<span class="bold">PMID: </span><a href="/pubmed/36601682" target="_blank">36601682</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32663356">Haematological manifestations of COVID-19: From cytopenia to coagulopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Agbuduwe C,
|
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Basu S</span><br />
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<span class="medgenPMjournal">Eur J Haematol</span>
|
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2020 Nov;105(5):540-546.
|
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Epub 2020 Aug 31
|
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doi: 10.1111/ejh.13491.
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<span class="bold">PMID: </span><a href="/pubmed/32663356" target="_blank">32663356</a><a href="/pmc/articles/PMC7404736" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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<div class="nl"><a target="_blank" href="/pubmed/8680517">Neonatal infections.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Greenough A</span><br />
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<span class="medgenPMjournal">Curr Opin Pediatr</span>
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1996 Feb;8(1):6-10.
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<span class="bold">PMID: </span><a href="/pubmed/8680517" target="_blank">8680517</a></div>
|
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neutrophilia%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (908)</a></div><h3 class="subhead">Diagnosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/38295127">Endotypes of occupational asthma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Mason P,
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Biasioli M,
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Liviero F</span><br />
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2024 Apr 1;24(2):58-63.
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Epub 2024 Jan 30
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doi: 10.1097/ACI.0000000000000969.
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<span class="bold">PMID: </span><a href="/pubmed/38295127" target="_blank">38295127</a><a href="/pmc/articles/PMC10916750" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/38066919">Atypical CML: diagnosis and treatment.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Breccia M</span><br />
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<span class="medgenPMjournal">Hematology Am Soc Hematol Educ Program</span>
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2023 Dec 8;2023(1):476-482.
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doi: 10.1182/hematology.2023000448.
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<span class="bold">PMID: </span><a href="/pubmed/38066919" target="_blank">38066919</a><a href="/pmc/articles/PMC10727105" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/26826881">Sweet Syndrome: A Review and Update.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Villarreal-Villarreal CD,
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Ocampo-Candiani J,
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<div class="nl"><a target="_blank" href="/pubmed/24750674">Leukocytosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Chabot-Richards DS,
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<span class="medgenPMjournal">Int J Lab Hematol</span>
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<span class="bold">PMID: </span><a href="/pubmed/24750674" target="_blank">24750674</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/23351991">Leukocyte adhesion deficiencies.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">van de Vijver E,
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<span class="medgenPMjournal">Hematol Oncol Clin North Am</span>
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<span class="bold">PMID: </span><a href="/pubmed/23351991" target="_blank">23351991</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neutrophilia%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (882)</a></div><h3 class="subhead">Therapy</h3>
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<div class="nl"><a target="_blank" href="/pubmed/38295127">Endotypes of occupational asthma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Mason P,
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Biasioli M,
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Liviero F</span><br />
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<span class="medgenPMjournal">Curr Opin Allergy Clin Immunol</span>
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2024 Apr 1;24(2):58-63.
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Epub 2024 Jan 30
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doi: 10.1097/ACI.0000000000000969.
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<span class="bold">PMID: </span><a href="/pubmed/38295127" target="_blank">38295127</a><a href="/pmc/articles/PMC10916750" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/30995510">The Cytokines of Asthma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Lambrecht BN,
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Fahy JV</span><br />
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<span class="medgenPMjournal">Immunity</span>
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<span class="bold">PMID: </span><a href="/pubmed/30995510" target="_blank">30995510</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28784414">Neutrophilic Inflammation in Asthma and Association with Disease Severity.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Ray A,
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<span class="medgenPMjournal">Trends Immunol</span>
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2017 Dec;38(12):942-954.
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<span class="bold">PMID: </span><a href="/pubmed/28784414" target="_blank">28784414</a><a href="/pmc/articles/PMC5711587" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/22123660">Lithium in the treatment of neutropenia.</a></div>
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<span class="bold">PMID: </span><a href="/pubmed/22123660" target="_blank">22123660</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/6966179">Hemophilus vaginalis bacteremia.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Adeniyi-Jones C,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neutrophilia%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (818)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/38066919">Atypical CML: diagnosis and treatment.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Breccia M</span><br />
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<span class="medgenPMjournal">Hematology Am Soc Hematol Educ Program</span>
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2023 Dec 8;2023(1):476-482.
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doi: 10.1182/hematology.2023000448.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38066919" target="_blank">38066919</a><a href="/pmc/articles/PMC10727105" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37943073">Hepatic abscessation in dogs: A multicenter study of 56 cases (2010-2019).</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Burke JE,
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Hess RS,
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McEntee EP,
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Griffin MA,
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Harmon SM,
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Silverstein DC</span><br />
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<span class="medgenPMjournal">J Vet Emerg Crit Care (San Antonio)</span>
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2023 Nov-Dec;33(6):665-675.
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Epub 2023 Nov 9
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doi: 10.1111/vec.13340.
|
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<span class="bold">PMID: </span><a href="/pubmed/37943073" target="_blank">37943073</a></div>
|
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|
||
<div class="nl"><a target="_blank" href="/pubmed/35061227">Clinical Course and Characteristics of Generalized Pustular Psoriasis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Choon SE,
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Navarini AA,
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Pinter A</span><br />
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<span class="medgenPMjournal">Am J Clin Dermatol</span>
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Epub 2022 Jan 21
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doi: 10.1007/s40257-021-00654-z.
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<span class="bold">PMID: </span><a href="/pubmed/35061227" target="_blank">35061227</a><a href="/pmc/articles/PMC8801409" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32663356">Haematological manifestations of COVID-19: From cytopenia to coagulopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Agbuduwe C,
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Basu S</span><br />
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<span class="medgenPMjournal">Eur J Haematol</span>
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2020 Nov;105(5):540-546.
|
||
Epub 2020 Aug 31
|
||
doi: 10.1111/ejh.13491.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32663356" target="_blank">32663356</a><a href="/pmc/articles/PMC7404736" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23351991">Leukocyte adhesion deficiencies.</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">van de Vijver E,
|
||
van den Berg TK,
|
||
Kuijpers TW</span><br />
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<span class="medgenPMjournal">Hematol Oncol Clin North Am</span>
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2013 Feb;27(1):101-16, viii.
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Epub 2012 Nov 13
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doi: 10.1016/j.hoc.2012.10.001.
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<span class="bold">PMID: </span><a href="/pubmed/23351991" target="_blank">23351991</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neutrophilia%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (675)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38295187">Myeloid and lymphoid expression of C9orf72 regulates IL-17A signaling in mice.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Limone F,
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Couto A,
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Wang JY,
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Zhang Y,
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McCourt B,
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Huang C,
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Minkin A,
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Jani M,
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McNeer S,
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Keaney J,
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Gillet G,
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Gonzalez RL,
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Goodman WA,
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Kadiu I,
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Eggan K,
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<span class="medgenPMjournal">Sci Transl Med</span>
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2024 Jan 31;16(732):eadg7895.
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doi: 10.1126/scitranslmed.adg7895.
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<span class="bold">PMID: </span><a href="/pubmed/38295187" target="_blank">38295187</a><a href="/pmc/articles/PMC11247723" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38066919">Atypical CML: diagnosis and treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Breccia M</span><br />
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<span class="medgenPMjournal">Hematology Am Soc Hematol Educ Program</span>
|
||
2023 Dec 8;2023(1):476-482.
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doi: 10.1182/hematology.2023000448.
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||
<span class="bold">PMID: </span><a href="/pubmed/38066919" target="_blank">38066919</a><a href="/pmc/articles/PMC10727105" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37943073">Hepatic abscessation in dogs: A multicenter study of 56 cases (2010-2019).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Burke JE,
|
||
Hess RS,
|
||
McEntee EP,
|
||
Griffin MA,
|
||
Harmon SM,
|
||
Silverstein DC</span><br />
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<span class="medgenPMjournal">J Vet Emerg Crit Care (San Antonio)</span>
|
||
2023 Nov-Dec;33(6):665-675.
|
||
Epub 2023 Nov 9
|
||
doi: 10.1111/vec.13340.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37943073" target="_blank">37943073</a></div>
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|
||
<div class="nl"><a target="_blank" href="/pubmed/37439130">It's in the blood: a review of the hematological system in SARS-CoV-2-associated COVID-19.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Harte JV,
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<span class="bold">PMID: </span><a href="/pubmed/37439130" target="_blank">37439130</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/35775497">Calprotectin in nasal secretion: a new biomarker of non-type 2 inflammation in CRSwNP.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">De Corso E,
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Baroni S,
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Onori ME,
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Tricarico L,
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Settimi S,
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Moretti G,
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Troiani E,
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Mastrapasqua RF,
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Furno D,
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Crudo F,
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Urbani A,
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Galli J</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/35775497" target="_blank">35775497</a><a href="/pmc/articles/PMC9577689" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neutrophilia%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (817)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/39704328">Molecular Characteristics of Sweet Syndrome: A Systematic Review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Calabrese L,
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Romagnuolo M,
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D'Onghia M,
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Rubegni P,
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Marzano AV,
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Moltrasio C</span><br />
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<span class="medgenPMjournal">Exp Dermatol</span>
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2024 Dec;33(12):e70022.
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<span class="bold">PMID: </span><a href="/pubmed/39704328" target="_blank">39704328</a><a href="/pmc/articles/PMC11660222" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/34260778">Immunity and inflammatory biomarkers in COVID-19: A systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Iwamura APD,
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Tavares da Silva MR,
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Hümmelgen AL,
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Soeiro Pereira PV,
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Falcai A,
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Grumach AS,
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Goudouris E,
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Neto AC,
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Prando C</span><br />
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<span class="medgenPMjournal">Rev Med Virol</span>
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<span class="bold">PMID: </span><a href="/pubmed/34260778" target="_blank">34260778</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32921706">Lymphopenia and neutrophilia at admission predicts severity and mortality in patients with COVID-19: a meta-analysis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Henry B,
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Cheruiyot I,
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Vikse J,
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Mutua V,
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Kipkorir V,
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Benoit J,
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Plebani M,
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Bragazzi N,
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<span class="medgenPMjournal">Acta Biomed</span>
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<div class="nl"><a target="_blank" href="/pubmed/30758455">Human exposure to mercury and its hematological effects: a systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Vianna ADS,
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Matos EP,
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Jesus IM,
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Asmus CIRF,
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Câmara VM</span><br />
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<span class="medgenPMjournal">Cad Saude Publica</span>
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2019 Feb 11;35(2):e00091618.
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<span class="bold">PMID: </span><a href="/pubmed/30758455" target="_blank">30758455</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28439845">A Systematic Review of the Clinical Presentation, Diagnosis, and Treatment of Small Bowel Obstruction.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Rami Reddy SR,
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|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neutrophilia%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (16)</a></div></div>
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