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<meta name="keywords" content="C1857632, finding, narrow hand, narrow hands, narrow palm, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="For children from birth to 4 years of age, the palm width is more than 2 SD below the mean; for children from 4 to 16 years of age the palm width is below the 5th centile; or, the width of the palm appears disproportionately narrow for its length." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
|
||
UID=346628
|
||
ConceptID=C1857632
|
||
-->
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||
<!--imgCountBooks = 0--><div class="ncbi_carousel" data-ncbicarousel-config="imageWidth:'100px',numItemsVisible:2,toggler:false"><div class="nc_header"><span class="img_strip_title">Image</span></div><div class="nc_content"><div class="nc_item"><a class="figpopup"><img alt="Figure 1" src="/projects/medgen/images/thumb/d60a47d140aab2a8.1.thumb.jpg" src-large="/projects/medgen/images/d60a47d140aab2a8.1.jpg" /></a><br /><a href="http://elementsofmorphology.nih.gov/index.cgi?tid=d60a47d140aab2a8" target="_blank" title="Elements of Morphology: Human Malformation Terminology - NHGRI">details</a></div></div></div><h1 class="medgenTitle"><div class="MedGenTitleText">Narrow palm</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>346628</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.">C1857632</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Narrow hands</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0004283">HP:0004283</a></td></tr>
|
||
</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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||
<div class="portlet mgSection" id="ID_100">
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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">For children from birth to 4 years of age, the palm width is more than 2 SD below the mean; for children from 4 to 16 years of age the palm width is below the 5th centile; or, the width of the palm appears disproportionately narrow for its length. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
||
</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>
|
||
<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 Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1857632[DISCUI]&test_type=Clinical" ref="ncbi_uid=346628">C</a></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">Narrow palm</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/536898" ref="tree=MeSH" title="MedGen record for Abnormality of limbs">Abnormality of limbs</a></span><ul><li><span class="TLline"><a href="/medgen/866555" ref="tree=MeSH" title="MedGen record for Abnormality of the upper limb">Abnormality of the upper limb</a></span><ul><li><span class="TLline"><a href="/medgen/6715" ref="tree=MeSH" title="MedGen record for Abnormality of the hand">Abnormality of the hand</a></span><ul><li><span class="TLline"><a href="/medgen/867564" ref="tree=MeSH" title="MedGen record for Abnormal palm morphology">Abnormal palm morphology</a></span><ul><li><span class="matched_ds">Narrow palm</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<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>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_46057"><div><strong>Prader-Willi syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>46057</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.">C0032897</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Prader-Willi syndrome (PWS) is characterized by severe hypotonia, poor appetite, and feeding difficulties in early infancy, followed in early childhood by excessive eating and gradual development of morbid obesity (unless food intake is strictly controlled). Motor milestones and language development are delayed. All individuals have some degree of cognitive impairment. Hypogonadism is present in both males and females and manifests as genital hypoplasia, incomplete pubertal development, and, in most, infertility. Short stature is common (if not treated with growth hormone). A distinctive behavioral phenotype (temper tantrums, stubbornness, manipulative behavior, and obsessive-compulsive characteristics) is common. Characteristic facial features, strabismus, and scoliosis are often present.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/46057">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_78539"><div><strong>Cohen syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>78539</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."><span class="highlight" style="background-color:">C0265223</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cohen syndrome is characterized by failure to thrive in infancy and childhood; truncal obesity in the teen years; early-onset hypotonia and developmental delays; microcephaly developing during the first year of life; moderate to profound psychomotor retardation; progressive retinochoroidal dystrophy and high myopia; neutropenia in many with recurrent infections and aphthous ulcers in some; a cheerful disposition; joint hypermobility; and characteristic facial features.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/78539">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_162918"><div><strong>Syndromic X-linked intellectual disability Snyder type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>162918</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.">C0796160</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Snyder-Robinson syndrome (SRS) is an X-linked intellectual disability syndrome characterized by asthenic build, facial dysmorphism with a prominent lower lip, kyphoscoliosis, osteoporosis, speech abnormalities, and seizures. Developmental delay usually presents as failure to meet early developmental milestones and then evolves to moderate to profound intellectual disability (which appears to remain stable over time) and variable motor disability. Asthenic habitus and low muscle mass usually develop during the first year, even in males who are ambulatory. During the first decade, males with SRS develop osteoporosis, resulting in fractures in the absence of trauma.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/162918">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_343403"><div><strong>Oculocerebrofacial syndrome, Kaufman type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>343403</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.">C1855663</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Kaufman oculocerebrofacial syndrome (KOS) is characterized by developmental delay, severe intellectual disability, and distinctive craniofacial features. Most affected children have prenatal-onset microcephaly, hypotonia, and growth deficiency. Feeding issues, ocular abnormalities, hearing impairment, and respiratory tract abnormalities are common. Ocular abnormalities can include structural abnormalities (microcornea or microphthalmia, coloboma, optic nerve hypoplasia), refractive errors (myopia ± astigmatism, hyperopia), strabismus, and entropion. Both conductive and sensorineural hearing loss have been reported as well as mixed conductive-sensorineural hearing loss of variable severity. Breathing problems can lead to prolonged hospitalization after birth in more than half of individuals. Less common findings include ectodermal abnormalities, cardiac manifestations, urogenital abnormalities, seizures, and skeletal abnormalities.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/343403">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_355853"><div><strong>Koolen-de Vries syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>355853</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.">C1864871</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Koolen-de Vries syndrome (KdVS) is characterized by congenital malformations, developmental delay / intellectual disability, neonatal/childhood hypotonia, epilepsy, dysmorphisms, and behavioral features. Psychomotor developmental delay is noted in all individuals from an early age. The majority of individuals with KdVS function in the mild-to-moderate range of intellectual disability. Other findings include speech and language delay (100%), epilepsy (~33%), congenital heart defects (25%-50%), renal and urologic anomalies (25%-50%), and cryptorchidism. Behavior in most is described as friendly, amiable, and cooperative.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/355853">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934741"><div><strong>Intellectual disability, autosomal dominant 42</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934741</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.">C4310774</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">GNB1 encephalopathy (GNB1-E) is characterized by moderate-to-severe developmental delay / intellectual disability, structural brain abnormalities, and often infantile hypotonia and seizures. Other less common findings include dystonia, reduced vision, behavior issues, growth delay, gastrointestinal (GI) problems, genitourinary (GU) abnormalities in males, and cutaneous mastocytosis.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934741">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794149"><div><strong>Ritscher-Schinzel syndrome 4</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794149</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.">C5561939</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Ritscher-Schinzel syndrome-4 (RTSC4) is characterized by a constellation of congenital anomalies, including dysmorphic craniofacial features and structural brain anomalies, such as Dandy-Walker malformation (220200), hindbrain malformations, or agenesis of the corpus callosum, associated with global developmental delay and impaired intellectual development. Congenital cardiac defects have been reported in 1 family (summary by Ritscher et al., 1987 and Jeanne et al., 2021). For a discussion of genetic heterogeneity of Ritscher-Schinzel syndrome, see RTSC1 (220210).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794149">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1807366"><div><strong>Schaaf-Yang syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1807366</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.">C5575066</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Schaaf-Yang syndrome (SYS) is a rare neurodevelopmental disorder that shares multiple clinical features with the genetically related Prader-Willi syndrome. It usually manifests at birth with muscular hypotonia in all and distal joint contractures in a majority of affected individuals. Gastrointestinal/feeding problems are particularly pronounced in infancy and childhood, but can transition to hyperphagia and obesity in adulthood. Respiratory distress is present in many individuals at birth, with approximately half requiring intubation and mechanical ventilation, and approximately 20% requiring tracheostomy. Skeletal manifestations such as joint contractures, scoliosis, and decreased bone mineral density are frequently observed. All affected individuals show developmental delay, resulting in intellectual disability of variable degree, from low-normal intelligence to severe intellectual disability. Other findings may include short stature, seizures, eye anomalies, and hypogonadism.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1807366">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1802176"><div><strong>Intellectual developmental disorder, autosomal dominant 68</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1802176</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.">C5677008</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal dominant intellectual developmental disorder-68 (MRD68) is characterized by developmental delay/intellectual disability, microcephaly, poor growth, feeding difficulties, and dysmorphic features. Some patients may have autism spectrum disorder or attention deficit-hyperactivity disorder (ADHD) (Cif et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1802176">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_78539" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cohen syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1802176" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual developmental disorder, autosomal dominant 68</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934741" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, autosomal dominant 42</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_355853" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Koolen-de Vries syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_343403" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Oculocerebrofacial syndrome, Kaufman type</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (9)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_46057" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Prader-Willi syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794149" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ritscher-Schinzel syndrome 4</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1807366" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Schaaf-Yang syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_162918" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Syndromic X-linked intellectual disability Snyder type</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<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>
|
||
<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/37345871">Serenoa repens for the treatment of lower urinary tract symptoms due to benign prostatic enlargement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Franco JV,
|
||
Trivisonno L,
|
||
Sgarbossa NJ,
|
||
Alvez GA,
|
||
Fieiras C,
|
||
Escobar Liquitay CM,
|
||
Jung JH</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2023 Jun 22;6(6):CD001423.
|
||
doi: 10.1002/14651858.CD001423.pub4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37345871" target="_blank">37345871</a><a href="/pmc/articles/PMC10286776" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(narrow%20palm)%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 (1)</a></div></div>
|
||
</div>
|
||
<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
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<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/37345871">Serenoa repens for the treatment of lower urinary tract symptoms due to benign prostatic enlargement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Franco JV,
|
||
Trivisonno L,
|
||
Sgarbossa NJ,
|
||
Alvez GA,
|
||
Fieiras C,
|
||
Escobar Liquitay CM,
|
||
Jung JH</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2023 Jun 22;6(6):CD001423.
|
||
doi: 10.1002/14651858.CD001423.pub4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37345871" target="_blank">37345871</a><a href="/pmc/articles/PMC10286776" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36724686">Determination of lithium concentration in capillary blood using volumetric dried blood spots.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wikström F,
|
||
Olsson C,
|
||
Palm B,
|
||
Roxhed N,
|
||
Backlund L,
|
||
Schalling M,
|
||
Beck O</span><br />
|
||
<span class="medgenPMjournal">J Pharm Biomed Anal</span>
|
||
2023 Apr 1;227:115269.
|
||
Epub 2023 Jan 29
|
||
doi: 10.1016/j.jpba.2023.115269.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36724686" target="_blank">36724686</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25203410">Fidaxomicin: a novel macrolide antibiotic for Clostridium difficile infection.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chahine EB,
|
||
Sucher AJ,
|
||
Mantei K</span><br />
|
||
<span class="medgenPMjournal">Consult Pharm</span>
|
||
2014 Sep;29(9):614-24.
|
||
doi: 10.4140/TCP.n.2014.614..
|
||
<span class="bold">PMID: </span><a href="/pubmed/25203410" target="_blank">25203410</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20861179">Drug interactions in metastatic breast cancer.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tyler T</span><br />
|
||
<span class="medgenPMjournal">J Oncol Pharm Pract</span>
|
||
2011 Sep;17(3):236-45.
|
||
Epub 2010 Sep 22
|
||
doi: 10.1177/1078155210379167.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20861179" target="_blank">20861179</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10880789">Task dependence of Ia presynaptic inhibition in human wrist extensor muscles: a single motor unit study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aimonetti JM,
|
||
Vedel JP,
|
||
Schmied A,
|
||
Pagni S</span><br />
|
||
<span class="medgenPMjournal">Clin Neurophysiol</span>
|
||
2000 Jul;111(7):1165-74.
|
||
doi: 10.1016/s1388-2457(00)00293-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10880789" target="_blank">10880789</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Narrow%20palm%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 (22)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37543774">Anomaly originated flexor digitorum superficialis muscle of the small finger: A case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lee YK</span><br />
|
||
<span class="medgenPMjournal">Medicine (Baltimore)</span>
|
||
2023 Aug 4;102(31):e34566.
|
||
doi: 10.1097/MD.0000000000034566.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37543774" target="_blank">37543774</a><a href="/pmc/articles/PMC10402993" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37345871">Serenoa repens for the treatment of lower urinary tract symptoms due to benign prostatic enlargement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Franco JV,
|
||
Trivisonno L,
|
||
Sgarbossa NJ,
|
||
Alvez GA,
|
||
Fieiras C,
|
||
Escobar Liquitay CM,
|
||
Jung JH</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2023 Jun 22;6(6):CD001423.
|
||
doi: 10.1002/14651858.CD001423.pub4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37345871" target="_blank">37345871</a><a href="/pmc/articles/PMC10286776" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26341359">Dermoscopic features of acral pigmented lesions in Egyptian patients: a descriptive study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Elwan NM,
|
||
Eltatawy RA,
|
||
Elfar NN,
|
||
Elsakka OM</span><br />
|
||
<span class="medgenPMjournal">Int J Dermatol</span>
|
||
2016 Feb;55(2):187-92.
|
||
Epub 2015 Sep 4
|
||
doi: 10.1111/ijd.12882.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26341359" target="_blank">26341359</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24513094">Risk factors for optic disc hemorrhage in the low-pressure glaucoma treatment study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Furlanetto RL,
|
||
De Moraes CG,
|
||
Teng CC,
|
||
Liebmann JM,
|
||
Greenfield DS,
|
||
Gardiner SK,
|
||
Ritch R,
|
||
Krupin T;
|
||
Low-Pressure Glaucoma Treatment Study Group</span><br />
|
||
<span class="medgenPMjournal">Am J Ophthalmol</span>
|
||
2014 May;157(5):945-52.
|
||
Epub 2014 Feb 7
|
||
doi: 10.1016/j.ajo.2014.02.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24513094" target="_blank">24513094</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8921187">Continuous beds for microchromatography: detection of proteins by a blotting membrane technique.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liao JL,
|
||
Zeng CM,
|
||
Palm A,
|
||
Hjertén S</span><br />
|
||
<span class="medgenPMjournal">Anal Biochem</span>
|
||
1996 Oct 15;241(2):195-8.
|
||
doi: 10.1006/abio.1996.0399.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8921187" target="_blank">8921187</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Narrow%20palm%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 (14)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37432742">Allosteric modulator potentiates β2AR agonist-promoted bronchoprotection in asthma models.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ahn S,
|
||
Maarsingh H,
|
||
Walker JK,
|
||
Liu S,
|
||
Hegde A,
|
||
Sumajit HC,
|
||
Kahsai AW,
|
||
Lefkowitz RJ</span><br />
|
||
<span class="medgenPMjournal">J Clin Invest</span>
|
||
2023 Sep 15;133(18)
|
||
doi: 10.1172/JCI167337.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37432742" target="_blank">37432742</a><a href="/pmc/articles/PMC10503797" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37345871">Serenoa repens for the treatment of lower urinary tract symptoms due to benign prostatic enlargement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Franco JV,
|
||
Trivisonno L,
|
||
Sgarbossa NJ,
|
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Alvez GA,
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Fieiras C,
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Escobar Liquitay CM,
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Jung JH</span><br />
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|
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doi: 10.1002/14651858.CD001423.pub4.
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<span class="bold">PMID: </span><a href="/pubmed/37345871" target="_blank">37345871</a><a href="/pmc/articles/PMC10286776" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33303818">Surface functionalisation of poly-APO-b-polyol ester cross-linked copolymers as core-shell nanoparticles for targeted breast cancer therapy.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Tajau R,
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<span class="bold">PMID: </span><a href="/pubmed/33303818" target="_blank">33303818</a><a href="/pmc/articles/PMC7729971" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/25203410">Fidaxomicin: a novel macrolide antibiotic for Clostridium difficile infection.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Chahine EB,
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<span class="bold">PMID: </span><a href="/pubmed/25203410" target="_blank">25203410</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/20861179">Drug interactions in metastatic breast cancer.</a></div>
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<span class="bold">PMID: </span><a href="/pubmed/20861179" target="_blank">20861179</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Narrow%20palm%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 (16)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/37553619">Identification of radiomic biomarkers in a set of four skeletal muscle groups on Dixon MRI of the NAKO MR study.</a></div>
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Küstner T,
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doi: 10.1186/s12880-023-01056-9.
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<span class="bold">PMID: </span><a href="/pubmed/37553619" target="_blank">37553619</a><a href="/pmc/articles/PMC10408104" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36724686">Determination of lithium concentration in capillary blood using volumetric dried blood spots.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wikström F,
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Olsson C,
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Palm B,
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Roxhed N,
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2023 Apr 1;227:115269.
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Epub 2023 Jan 29
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doi: 10.1016/j.jpba.2023.115269.
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<span class="bold">PMID: </span><a href="/pubmed/36724686" target="_blank">36724686</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/31722839">Randomized Clinical Trial Representativeness and Outcomes in Real-World Patients: Comparison of 6 Hallmark Randomized Clinical Trials of Relapsed/Refractory Multiple Myeloma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Chari A,
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Romanus D,
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Palumbo A,
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Blazer M,
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Farrelly E,
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Raju A,
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Huang H,
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Richardson P</span><br />
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<span class="medgenPMjournal">Clin Lymphoma Myeloma Leuk</span>
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2020 Jan;20(1):8-17.e16.
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Epub 2019 Oct 10
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doi: 10.1016/j.clml.2019.09.625.
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<span class="bold">PMID: </span><a href="/pubmed/31722839" target="_blank">31722839</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/24513094">Risk factors for optic disc hemorrhage in the low-pressure glaucoma treatment study.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Furlanetto RL,
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De Moraes CG,
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Teng CC,
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Liebmann JM,
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Greenfield DS,
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Gardiner SK,
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Ritch R,
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Krupin T;
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<span class="medgenPMjournal">Am J Ophthalmol</span>
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2014 May;157(5):945-52.
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Epub 2014 Feb 7
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doi: 10.1016/j.ajo.2014.02.009.
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||
<span class="bold">PMID: </span><a href="/pubmed/24513094" target="_blank">24513094</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8374451">Relation of fingerprints and shape of the palm to fetal growth and adult blood pressure.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Godfrey KM,
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Barker DJ,
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Peace J,
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<span class="bold">PMID: </span><a href="/pubmed/8374451" target="_blank">8374451</a><a href="/pmc/articles/PMC1678406" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Narrow%20palm%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 (12)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
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<div class="nl"><a target="_blank" href="/pubmed/37543774">Anomaly originated flexor digitorum superficialis muscle of the small finger: A case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lee YK</span><br />
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<span class="medgenPMjournal">Medicine (Baltimore)</span>
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||
2023 Aug 4;102(31):e34566.
|
||
doi: 10.1097/MD.0000000000034566.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37543774" target="_blank">37543774</a><a href="/pmc/articles/PMC10402993" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37345871">Serenoa repens for the treatment of lower urinary tract symptoms due to benign prostatic enlargement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Franco JV,
|
||
Trivisonno L,
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||
Sgarbossa NJ,
|
||
Alvez GA,
|
||
Fieiras C,
|
||
Escobar Liquitay CM,
|
||
Jung JH</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2023 Jun 22;6(6):CD001423.
|
||
doi: 10.1002/14651858.CD001423.pub4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37345871" target="_blank">37345871</a><a href="/pmc/articles/PMC10286776" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16434441">CSS-Palm: palmitoylation site prediction with a clustering and scoring strategy (CSS).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhou F,
|
||
Xue Y,
|
||
Yao X,
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Xu Y</span><br />
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<span class="medgenPMjournal">Bioinformatics</span>
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||
2006 Apr 1;22(7):894-6.
|
||
Epub 2006 Jan 24
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||
doi: 10.1093/bioinformatics/btl013.
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||
<span class="bold">PMID: </span><a href="/pubmed/16434441" target="_blank">16434441</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10880789">Task dependence of Ia presynaptic inhibition in human wrist extensor muscles: a single motor unit study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aimonetti JM,
|
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Vedel JP,
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||
Schmied A,
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Pagni S</span><br />
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<span class="medgenPMjournal">Clin Neurophysiol</span>
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2000 Jul;111(7):1165-74.
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||
doi: 10.1016/s1388-2457(00)00293-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10880789" target="_blank">10880789</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9216491">Task-dependence of muscle afferent monosynaptic inputs to human extensor carpi radialis motoneurones.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schmied A,
|
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Vedel JP,
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Calvin-Figuière S,
|
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Rossi-Durand C,
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Pagni S</span><br />
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|
||
<span class="bold">PMID: </span><a href="/pubmed/9216491" target="_blank">9216491</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Narrow%20palm%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 (17)</a></div></div>
|
||
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|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
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<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/37345871">Serenoa repens for the treatment of lower urinary tract symptoms due to benign prostatic enlargement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Franco JV,
|
||
Trivisonno L,
|
||
Sgarbossa NJ,
|
||
Alvez GA,
|
||
Fieiras C,
|
||
Escobar Liquitay CM,
|
||
Jung JH</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2023 Jun 22;6(6):CD001423.
|
||
doi: 10.1002/14651858.CD001423.pub4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37345871" target="_blank">37345871</a><a href="/pmc/articles/PMC10286776" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Narrow%20palm%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 (1)</a></div></div>
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|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C1857632%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (2)</a></li>
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<li><a href="/gtr/tests?term=C1857632%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (2)</a></li>
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<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C1857632%5bDISCUI%5d" target="_blank">See all (2)</a></total></li>
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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Narrow%20palm" target="_blank">MedlinePlus</a></li></ul></div>
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<a href="/pubmed/clinical?term=Narrow%20palm" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Narrow%20palm%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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