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<!--
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UID=344477
|
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ConceptID=C1855331
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Olfactory lobe agenesis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>344477</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.">C1855331</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
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<td>Olfactory lobe absence</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:0001341">HP:0001341</a></td></tr>
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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="TLline">Olfactory lobe agenesis</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span><ul><li><span class="TLline"><a href="/medgen/868416" ref="tree=MeSH" title="MedGen record for Abnormal nervous system morphology">Abnormal nervous system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892343" ref="tree=MeSH" title="MedGen record for Morphological central nervous system abnormality">Morphological central nervous system abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/866738" ref="tree=MeSH" title="MedGen record for Abnormal brain morphology">Abnormal brain morphology</a></span><ul><li><span class="TLline"><a href="/medgen/866620" ref="tree=MeSH" title="MedGen record for Abnormal forebrain morphology">Abnormal forebrain morphology</a></span><ul><li><span class="TLline"><a href="/medgen/1369989" ref="tree=MeSH" title="MedGen record for Abnormal olfactory lobe morphology">Abnormal olfactory lobe morphology</a></span><ul><li><span class="matched_ds">Olfactory lobe agenesis</span></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_295872"><div><strong>Hypogonadotropic hypogonadism 1 with or without anosmia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>295872</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.">C1563719</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Isolated gonadotropin-releasing hormone (GnRH) deficiency (IGD) is characterized by inappropriately low serum concentrations of the gonadotropins LH (luteinizing hormone) and FSH (follicle-stimulating hormone) in the presence of low circulating concentrations of sex steroids. IGD is associated with a normal sense of smell (normosmic IGD) in approximately 40% of affected individuals and an impaired sense of smell (Kallmann syndrome) in approximately 60%. IGD can first become apparent in infancy, adolescence, or adulthood. Infant boys with congenital IGD often have micropenis and cryptorchidism. Adolescents and adults with IGD have clinical evidence of hypogonadism and incomplete sexual maturation on physical examination. Adult males with IGD tend to have prepubertal testicular volume (i.e., <4 mL), absence of secondary sexual features (e.g., facial and axillary hair growth, deepening of the voice), decreased muscle mass, diminished libido, erectile dysfunction, and infertility. Adult females have little or no breast development and primary amenorrhea. Although skeletal maturation is delayed, the rate of linear growth is usually normal except for the absence of a distinct pubertal growth spurt.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/295872">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_333437"><div><strong>Kallmann syndrome with spastic paraplegia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>333437</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.">C1839911</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/333437">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_477139"><div><strong>Multiple congenital anomalies-hypotonia-seizures syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>477139</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.">C3275508</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Multiple congenital anomalies-hypotonia-seizures syndrome-2 (MCAHS2) is an X-linked recessive neurodevelopmental disorder characterized by dysmorphic features, neonatal hypotonia, early-onset myoclonic seizures, and variable congenital anomalies involving the central nervous, cardiac, and urinary systems. Some affected individuals die in infancy (summary by Johnston et al., 2012). The phenotype shows clinical variability with regard to severity and extraneurologic features. However, most patients present in infancy with early-onset epileptic encephalopathy associated with developmental arrest and subsequent severe neurologic disability; these features are consistent with a form of developmental and epileptic encephalopathy (DEE) (summary by Belet et al., 2014, Kato et al., 2014). The disorder is caused by a defect in glycosylphosphatidylinositol (GPI) biosynthesis. For a discussion of genetic heterogeneity of MCAHS, see MCAHS1 (614080). For a discussion of nomenclature and genetic heterogeneity of DEE, see 308350. For a discussion of genetic heterogeneity of GPI biosynthesis defects, see GPIBD1 (610293).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/477139">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_811346"><div><strong>Meckel syndrome, type 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>811346</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.">C3714506</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Meckel syndrome, also known as Meckel-Gruber syndrome, is a severe pleiotropic autosomal recessive developmental disorder caused by dysfunction of primary cilia during early embryogenesis. There is extensive clinical variability and controversy as to the minimum diagnostic criteria. Early reports, including that of Opitz and Howe (1969) and Wright et al. (1994), stated that the classic triad of Meckel syndrome comprises (1) cystic renal disease; (2) a central nervous system malformation, most commonly occipital encephalocele; and (3) polydactyly, most often postaxial. However, based on a study of 67 patients, Salonen (1984) concluded that the minimum diagnostic criteria are (1) cystic renal disease; (2) CNS malformation, and (3) hepatic abnormalities, including portal fibrosis or ductal proliferation. In a review of Meckel syndrome, Logan et al. (2011) stated that the classic triad first described by Meckel (1822) included occipital encephalocele, cystic kidneys, and fibrotic changes to the liver. Genetic Heterogeneity of Meckel Syndrome See also MKS2 (603194), caused by mutation in the TMEM216 gene (613277) on chromosome 11q12; MKS3 (607361), caused by mutation in the TMEM67 gene (609884) on chromosome 8q; MKS4 (611134), caused by mutation in the CEP290 gene (610142) on chromosome 12q; MKS5 (611561), caused by mutation in the RPGRIP1L gene (610937) on chromosome 16q12; MKS6 (612284), caused by mutation in the CC2D2A gene (612013) on chromosome 4p15; MKS7 (267010), caused by mutation in the NPHP3 (608002) gene on chromosome 3q22; MKS8 (613885), caused by mutation in the TCTN2 gene (613846) on chromosome 12q24; MKS9 (614209), caused by mutation in the B9D1 gene (614144) on chromosome 17p11; MKS10 (614175), caused by mutation in the B9D2 gene (611951) on chromosome 19q13; MKS11 (615397), caused by mutation in the TMEM231 gene (614949) on chromosome 16q23; MKS12 (616258), caused by mutation in the KIF14 gene (611279) on chromosome 1q32; MKS13 (617562), caused by mutation in the TMEM107 gene (616183) on chromosome 17p13; and MKS14 (619879), caused by mutation in the TXNDC15 gene (617778) on chromosome 5q31.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/811346">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_295872" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypogonadotropic hypogonadism 1 with or without anosmia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_333437" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Kallmann syndrome with spastic paraplegia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_811346" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Meckel syndrome, type 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_477139" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Multiple congenital anomalies-hypotonia-seizures syndrome 2</a></div></div>
|
||
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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>
|
||
<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/28186656">Phenotype- and genotype-specific structural alterations in spasmodic dysphonia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bianchi S,
|
||
Battistella G,
|
||
Huddleston H,
|
||
Scharf R,
|
||
Fleysher L,
|
||
Rumbach AF,
|
||
Frucht SJ,
|
||
Blitzer A,
|
||
Ozelius LJ,
|
||
Simonyan K</span><br />
|
||
<span class="medgenPMjournal">Mov Disord</span>
|
||
2017 Apr;32(4):560-568.
|
||
Epub 2017 Feb 10
|
||
doi: 10.1002/mds.26920.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28186656" target="_blank">28186656</a><a href="/pmc/articles/PMC5578762" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23640781">Distortion of the anterior part of the interhemispheric fissure: significance and implications for prenatal diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vinurel N,
|
||
Van Nieuwenhuyse A,
|
||
Cagneaux M,
|
||
Garel C,
|
||
Quarello E,
|
||
Brasseur M,
|
||
Picone O,
|
||
Ferry M,
|
||
Gaucherand P,
|
||
des Portes V,
|
||
Guibaud L</span><br />
|
||
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
|
||
2014 Mar;43(3):346-52.
|
||
Epub 2014 Jan 2
|
||
doi: 10.1002/uog.12498.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23640781" target="_blank">23640781</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18511243">A magnetic resonance imaging study of the entorhinal cortex in treatment-resistant depression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Furtado CP,
|
||
Maller JJ,
|
||
Fitzgerald PB</span><br />
|
||
<span class="medgenPMjournal">Psychiatry Res</span>
|
||
2008 Jul 15;163(2):133-42.
|
||
Epub 2008 May 29
|
||
doi: 10.1016/j.pscychresns.2007.11.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18511243" target="_blank">18511243</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(olfactory%20lobe%20agenesis)%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 (3)</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/36825405">Single-cell sequencing of entorhinal cortex reveals widespread disruption of neuropeptide networks in Alzheimer's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Li M,
|
||
Larsen PA</span><br />
|
||
<span class="medgenPMjournal">Alzheimers Dement</span>
|
||
2023 Aug;19(8):3575-3592.
|
||
Epub 2023 Feb 24
|
||
doi: 10.1002/alz.12979.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36825405" target="_blank">36825405</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35255491">SARS-CoV-2 is associated with changes in brain structure in UK Biobank.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Douaud G,
|
||
Lee S,
|
||
Alfaro-Almagro F,
|
||
Arthofer C,
|
||
Wang C,
|
||
McCarthy P,
|
||
Lange F,
|
||
Andersson JLR,
|
||
Griffanti L,
|
||
Duff E,
|
||
Jbabdi S,
|
||
Taschler B,
|
||
Keating P,
|
||
Winkler AM,
|
||
Collins R,
|
||
Matthews PM,
|
||
Allen N,
|
||
Miller KL,
|
||
Nichols TE,
|
||
Smith SM</span><br />
|
||
<span class="medgenPMjournal">Nature</span>
|
||
2022 Apr;604(7907):697-707.
|
||
Epub 2022 Mar 7
|
||
doi: 10.1038/s41586-022-04569-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35255491" target="_blank">35255491</a><a href="/pmc/articles/PMC9046077" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34012420">Altered White Matter Microstructures in Type 2 Diabetes Mellitus: A Coordinate-Based Meta-Analysis of Diffusion Tensor Imaging Studies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhou C,
|
||
Li J,
|
||
Dong M,
|
||
Ping L,
|
||
Lin H,
|
||
Wang Y,
|
||
Wang S,
|
||
Gao S,
|
||
Yu G,
|
||
Cheng Y,
|
||
Xu X</span><br />
|
||
<span class="medgenPMjournal">Front Endocrinol (Lausanne)</span>
|
||
2021;12:658198.
|
||
Epub 2021 May 3
|
||
doi: 10.3389/fendo.2021.658198.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34012420" target="_blank">34012420</a><a href="/pmc/articles/PMC8127836" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33482355">T(1)AM-TAAR1 signalling protects against OGD-induced synaptic dysfunction in the entorhinal cortex.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tozzi F,
|
||
Rutigliano G,
|
||
Borsò M,
|
||
Falcicchia C,
|
||
Zucchi R,
|
||
Origlia N</span><br />
|
||
<span class="medgenPMjournal">Neurobiol Dis</span>
|
||
2021 Apr;151:105271.
|
||
Epub 2021 Jan 19
|
||
doi: 10.1016/j.nbd.2021.105271.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33482355" target="_blank">33482355</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29956611">Electrophysiological Characteristics of the Migraine Brain: Current Knowledge and Perspectives.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marucco E,
|
||
Lisicki M,
|
||
Magis D</span><br />
|
||
<span class="medgenPMjournal">Curr Med Chem</span>
|
||
2019;26(34):6222-6235.
|
||
doi: 10.2174/0929867325666180627130811.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29956611" target="_blank">29956611</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Olfactory%20lobe%20agenesis%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 (94)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36825405">Single-cell sequencing of entorhinal cortex reveals widespread disruption of neuropeptide networks in Alzheimer's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Li M,
|
||
Larsen PA</span><br />
|
||
<span class="medgenPMjournal">Alzheimers Dement</span>
|
||
2023 Aug;19(8):3575-3592.
|
||
Epub 2023 Feb 24
|
||
doi: 10.1002/alz.12979.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36825405" target="_blank">36825405</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35255491">SARS-CoV-2 is associated with changes in brain structure in UK Biobank.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Douaud G,
|
||
Lee S,
|
||
Alfaro-Almagro F,
|
||
Arthofer C,
|
||
Wang C,
|
||
McCarthy P,
|
||
Lange F,
|
||
Andersson JLR,
|
||
Griffanti L,
|
||
Duff E,
|
||
Jbabdi S,
|
||
Taschler B,
|
||
Keating P,
|
||
Winkler AM,
|
||
Collins R,
|
||
Matthews PM,
|
||
Allen N,
|
||
Miller KL,
|
||
Nichols TE,
|
||
Smith SM</span><br />
|
||
<span class="medgenPMjournal">Nature</span>
|
||
2022 Apr;604(7907):697-707.
|
||
Epub 2022 Mar 7
|
||
doi: 10.1038/s41586-022-04569-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35255491" target="_blank">35255491</a><a href="/pmc/articles/PMC9046077" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25968962">Olfaction and Aging: A Mini-Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Attems J,
|
||
Walker L,
|
||
Jellinger KA</span><br />
|
||
<span class="medgenPMjournal">Gerontology</span>
|
||
2015;61(6):485-90.
|
||
Epub 2015 May 9
|
||
doi: 10.1159/000381619.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25968962" target="_blank">25968962</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23932763">The olfactory system.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leboucq N,
|
||
Menjot de Champfleur N,
|
||
Menjot de Champfleur S,
|
||
Bonafé A</span><br />
|
||
<span class="medgenPMjournal">Diagn Interv Imaging</span>
|
||
2013 Oct;94(10):985-91.
|
||
Epub 2013 Aug 7
|
||
doi: 10.1016/j.diii.2013.06.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23932763" target="_blank">23932763</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9210754">Cytoarchitecture of the entorhinal cortex in schizophrenia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Akil M,
|
||
Lewis DA</span><br />
|
||
<span class="medgenPMjournal">Am J Psychiatry</span>
|
||
1997 Jul;154(7):1010-2.
|
||
doi: 10.1176/ajp.154.7.1010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9210754" target="_blank">9210754</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Olfactory%20lobe%20agenesis%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 (78)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36063364">Interventions for the prevention of persistent post-COVID-19 olfactory dysfunction.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Webster KE,
|
||
O'Byrne L,
|
||
MacKeith S,
|
||
Philpott C,
|
||
Hopkins C,
|
||
Burton MJ</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2022 Sep 5;9(9):CD013877.
|
||
doi: 10.1002/14651858.CD013877.pub3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36063364" target="_blank">36063364</a><a href="/pmc/articles/PMC9443936" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32589127">Central nervous system pathology in the amniotic rupture sequence.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shannon P</span><br />
|
||
<span class="medgenPMjournal">Clin Neuropathol</span>
|
||
2020 Nov/Dec;39(6):288-299.
|
||
doi: 10.5414/NP301266.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32589127" target="_blank">32589127</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25245197">Migraine is associated with altered processing of sensory stimuli.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Harriott AM,
|
||
Schwedt TJ</span><br />
|
||
<span class="medgenPMjournal">Curr Pain Headache Rep</span>
|
||
2014 Nov;18(11):458.
|
||
doi: 10.1007/s11916-014-0458-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25245197" target="_blank">25245197</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18511243">A magnetic resonance imaging study of the entorhinal cortex in treatment-resistant depression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Furtado CP,
|
||
Maller JJ,
|
||
Fitzgerald PB</span><br />
|
||
<span class="medgenPMjournal">Psychiatry Res</span>
|
||
2008 Jul 15;163(2):133-42.
|
||
Epub 2008 May 29
|
||
doi: 10.1016/j.pscychresns.2007.11.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18511243" target="_blank">18511243</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9460094">The volume of the entorhinal cortex in schizophrenia: a controlled MRI study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nasrallah HA,
|
||
Sharma S,
|
||
Olson SC</span><br />
|
||
<span class="medgenPMjournal">Prog Neuropsychopharmacol Biol Psychiatry</span>
|
||
1997 Nov;21(8):1317-22.
|
||
doi: 10.1016/s0278-5846(97)00166-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9460094" target="_blank">9460094</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Olfactory%20lobe%20agenesis%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 (23)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36825405">Single-cell sequencing of entorhinal cortex reveals widespread disruption of neuropeptide networks in Alzheimer's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Li M,
|
||
Larsen PA</span><br />
|
||
<span class="medgenPMjournal">Alzheimers Dement</span>
|
||
2023 Aug;19(8):3575-3592.
|
||
Epub 2023 Feb 24
|
||
doi: 10.1002/alz.12979.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36825405" target="_blank">36825405</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33784519">A1 Segment Unruptured Aneurysm of Persistent Primitive Olfactory Artery Coexisted with Accessory Middle Cerebral Artery.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ogawa Y,
|
||
Soejima K,
|
||
Kawahara I,
|
||
Shiozaki E,
|
||
Morofuji Y,
|
||
Ono T,
|
||
Haraguchi W,
|
||
Tsutsumi K</span><br />
|
||
<span class="medgenPMjournal">J Stroke Cerebrovasc Dis</span>
|
||
2021 Jun;30(6):105758.
|
||
Epub 2021 Mar 27
|
||
doi: 10.1016/j.jstrokecerebrovasdis.2021.105758.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33784519" target="_blank">33784519</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28641136">Age exacerbates abnormal protein expression in a mouse model of Down syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ahmed MM,
|
||
Block A,
|
||
Tong S,
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Davisson MT,
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Gardiner KJ</span><br />
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<span class="medgenPMjournal">Neurobiol Aging</span>
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2017 Sep;57:120-132.
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Epub 2017 May 10
|
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doi: 10.1016/j.neurobiolaging.2017.05.002.
|
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<span class="bold">PMID: </span><a href="/pubmed/28641136" target="_blank">28641136</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/21592598">Neurochemical alterations of the entorhinal cortex in amnestic mild cognitive impairment (aMCI): a three-year follow-up study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Seo SW,
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Lee JH,
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Jang SM,
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Kim ST,
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Chin J,
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Kim GH,
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Kim JH,
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Roh JH,
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Kim MJ,
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Kim SH,
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<span class="medgenPMjournal">Arch Gerontol Geriatr</span>
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2012 Jan-Feb;54(1):192-6.
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<span class="bold">PMID: </span><a href="/pubmed/21592598" target="_blank">21592598</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/18511243">A magnetic resonance imaging study of the entorhinal cortex in treatment-resistant depression.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Furtado CP,
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2008 Jul 15;163(2):133-42.
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Epub 2008 May 29
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doi: 10.1016/j.pscychresns.2007.11.005.
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<span class="bold">PMID: </span><a href="/pubmed/18511243" target="_blank">18511243</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Olfactory%20lobe%20agenesis%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 (36)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/36825405">Single-cell sequencing of entorhinal cortex reveals widespread disruption of neuropeptide networks in Alzheimer's disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Li M,
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Larsen PA</span><br />
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<span class="medgenPMjournal">Alzheimers Dement</span>
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2023 Aug;19(8):3575-3592.
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Epub 2023 Feb 24
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doi: 10.1002/alz.12979.
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<span class="bold">PMID: </span><a href="/pubmed/36825405" target="_blank">36825405</a></div>
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|
||
<div class="nl"><a target="_blank" href="/pubmed/35255491">SARS-CoV-2 is associated with changes in brain structure in UK Biobank.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Douaud G,
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Lee S,
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Alfaro-Almagro F,
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Arthofer C,
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Wang C,
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McCarthy P,
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Lange F,
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Andersson JLR,
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Griffanti L,
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Duff E,
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Jbabdi S,
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Taschler B,
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Keating P,
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Collins R,
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Miller KL,
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<span class="medgenPMjournal">Nature</span>
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2022 Apr;604(7907):697-707.
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Epub 2022 Mar 7
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doi: 10.1038/s41586-022-04569-5.
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<span class="bold">PMID: </span><a href="/pubmed/35255491" target="_blank">35255491</a><a href="/pmc/articles/PMC9046077" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/33482355">T(1)AM-TAAR1 signalling protects against OGD-induced synaptic dysfunction in the entorhinal cortex.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tozzi F,
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Rutigliano G,
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Borsò M,
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Falcicchia C,
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Zucchi R,
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Origlia N</span><br />
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<span class="medgenPMjournal">Neurobiol Dis</span>
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2021 Apr;151:105271.
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Epub 2021 Jan 19
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doi: 10.1016/j.nbd.2021.105271.
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<span class="bold">PMID: </span><a href="/pubmed/33482355" target="_blank">33482355</a></div>
|
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|
||
<div class="nl"><a target="_blank" href="/pubmed/28641136">Age exacerbates abnormal protein expression in a mouse model of Down syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ahmed MM,
|
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Block A,
|
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Tong S,
|
||
Davisson MT,
|
||
Gardiner KJ</span><br />
|
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<span class="medgenPMjournal">Neurobiol Aging</span>
|
||
2017 Sep;57:120-132.
|
||
Epub 2017 May 10
|
||
doi: 10.1016/j.neurobiolaging.2017.05.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28641136" target="_blank">28641136</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9210754">Cytoarchitecture of the entorhinal cortex in schizophrenia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Akil M,
|
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Lewis DA</span><br />
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<span class="medgenPMjournal">Am J Psychiatry</span>
|
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1997 Jul;154(7):1010-2.
|
||
doi: 10.1176/ajp.154.7.1010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9210754" target="_blank">9210754</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Olfactory%20lobe%20agenesis%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 (88)</a></div></div>
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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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|
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<div class="nl"><a target="_blank" href="/pubmed/39667073">Gray matter structural alterations in idiopathic rapid eye movement sleep behavior disorder: A voxel-based meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang X,
|
||
Li Y,
|
||
Li B,
|
||
Shang H,
|
||
Yang J</span><br />
|
||
<span class="medgenPMjournal">Sleep Med</span>
|
||
2025 Feb;126:114-121.
|
||
Epub 2024 Dec 4
|
||
doi: 10.1016/j.sleep.2024.12.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39667073" target="_blank">39667073</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36063364">Interventions for the prevention of persistent post-COVID-19 olfactory dysfunction.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Webster KE,
|
||
O'Byrne L,
|
||
MacKeith S,
|
||
Philpott C,
|
||
Hopkins C,
|
||
Burton MJ</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2022 Sep 5;9(9):CD013877.
|
||
doi: 10.1002/14651858.CD013877.pub3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36063364" target="_blank">36063364</a><a href="/pmc/articles/PMC9443936" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34291812">Interventions for the prevention of persistent post-COVID-19 olfactory dysfunction.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Webster KE,
|
||
O'Byrne L,
|
||
MacKeith S,
|
||
Philpott C,
|
||
Hopkins C,
|
||
Burton MJ</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2021 Jul 22;7(7):CD013877.
|
||
doi: 10.1002/14651858.CD013877.pub2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34291812" target="_blank">34291812</a><a href="/pmc/articles/PMC8406518" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/34012420">Altered White Matter Microstructures in Type 2 Diabetes Mellitus: A Coordinate-Based Meta-Analysis of Diffusion Tensor Imaging Studies.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Zhou C,
|
||
Li J,
|
||
Dong M,
|
||
Ping L,
|
||
Lin H,
|
||
Wang Y,
|
||
Wang S,
|
||
Gao S,
|
||
Yu G,
|
||
Cheng Y,
|
||
Xu X</span><br />
|
||
<span class="medgenPMjournal">Front Endocrinol (Lausanne)</span>
|
||
2021;12:658198.
|
||
Epub 2021 May 3
|
||
doi: 10.3389/fendo.2021.658198.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34012420" target="_blank">34012420</a><a href="/pmc/articles/PMC8127836" 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=%22Olfactory%20lobe%20agenesis%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 (4)</a></div></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(olfactory%20lobe%20agenesis)%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">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Olfactory%20lobe%20agenesis%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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