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<!--
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UID=322038
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ConceptID=C1832776
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Hypertrophic nerve changes</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>322038</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.">C1832776</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><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:0003382">HP:0003382</a></td></tr>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Hypertrophic nerve changes</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/871309" ref="tree=MeSH" title="MedGen record for Abnormality of prenatal development or birth">Abnormality of prenatal development or birth</a></span><ul><li><span class="TLline"><a href="/medgen/1254" ref="tree=MeSH" title="MedGen record for Fetal anomaly">Fetal anomaly</a></span><ul><li><span class="TLline"><a href="/medgen/474891" ref="tree=MeSH" title="MedGen record for Congenital Systemic Disorder">Congenital Systemic Disorder</a></span><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/892389" ref="tree=MeSH" title="MedGen record for Abnormal peripheral nervous system morphology">Abnormal peripheral nervous system morphology</a></span><ul><li><span class="matched_ds">Hypertrophic nerve changes</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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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_3710"><div><strong>Dejerine-Sottas disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>3710</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.">C0011195</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Dejerine-Sottas neuropathy is a demyelinating peripheral neuropathy with onset in infancy. It can show autosomal dominant or recessive inheritance. Affected individuals have delayed motor development due to severe distal motor and sensory impairment, resulting in difficulties in gait. Some patients have generalized hypotonia in infancy. Other features may include pes cavus, scoliosis, and sensory ataxia. Nerve conduction velocities are severely decreased (sometimes less than 10 m/s), and sural nerve biopsy shows severe loss of myelinated fibers (summary by Baets et al., 2011).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/3710">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_64430"><div><strong>Roussy-Lévy syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>64430</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.">C0205713</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Roussy-Levy syndrome is an autosomal dominant disorder characterized by early onset of prominent ataxia followed by late onset of mild motor involvement. Symptoms progress very slowly, and affected individuals may remain ambulatory throughout life (Auer-Grumbach et al., 1998; Plante-Bordeneuve et al., 1999).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/64430">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_75727"><div><strong>Charcot-Marie-Tooth disease, type IA</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75727</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.">C0270911</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">For a general phenotypic description and a discussion of genetic heterogeneity of Charcot-Marie-Tooth disease type 1, see CMT1B (118200). CMT1A is the most common form of CMT. The average age of onset of clinical symptoms is 12.2 +/- 7.3 years. Slow nerve conduction velocity (NCV) less than 38 m/s is highly diagnostic and is a 100% penetrant phenotype independent of age (Lupski et al., 1991, 1992).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75727">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_124377"><div><strong>Charcot-Marie-Tooth disease type 1B</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>124377</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.">C0270912</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Charcot-Marie-Tooth disease is a sensorineural peripheral polyneuropathy. Affecting approximately 1 in 2,500 individuals, Charcot-Marie-Tooth disease is the most common inherited disorder of the peripheral nervous system (Skre, 1974). Autosomal dominant, autosomal recessive, and X-linked forms have been recognized. Classification On the basis of electrophysiologic properties and histopathology, CMT has been divided into primary peripheral demyelinating (type 1, or HMSNI) and primary peripheral axonal (type 2, or HMSNII) neuropathies. The demyelinating neuropathies classified as CMT type 1 are characterized by severely reduced motor NCVs (less than 38 m/s) and segmental demyelination and remyelination with onion bulb formations on nerve biopsy. The axonal neuropathies classified as CMT type 2 are characterized by normal or mildly reduced NCVs and chronic axonal degeneration and regeneration on nerve biopsy (see CMT2A1; 118210). Distal hereditary motor neuropathy (dHMN) (see 158590), or spinal CMT, is characterized by exclusive motor involvement and sparing of sensory nerves (Pareyson, 1999). McAlpine (1989) proposed that the forms of CMT with very slow nerve conduction be given the gene symbol CMT1A (118220) and CMT1B, CMT1A being the gene on chromosome 17 and CMT1B being the gene on chromosome 1. CMT2 was the proposed symbol for the autosomal locus responsible for the moderately slow nerve conduction form of the disease (axonal). For a phenotypic description and discussion of genetic heterogeneity of the various subtypes of CMT, see CMTX1 (302800), CMT2A1 (118210), CMT3 (DSS; 145900), CMT4A (214400), and CMTDIB (606482). Genetic Heterogeneity of Autosomal Dominant Demyelinating CMT1 Autosomal dominant demyelinating CMT1 is a genetically heterogeneous disorder and can be caused by mutations in different genes; see CMT1A (118220), CMT1C (601098), CMT1D (607678), CMT1E (607734), CMT1F (607734), CMT1G (618279), CMT1H (619764), CMT1I (619742), and CMT1J (620111). See also 608236 for a related phenotype characterized by isolated slowed nerve conduction velocities (NCVs).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/124377">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_75728"><div><strong>Charcot-Marie-Tooth disease type 1C</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75728</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.">C0270913</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">For a phenotypic description and a discussion of genetic heterogeneity of autosomal dominant Charcot-Marie-Tooth disease type 1, see CMT1B (118200).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75728">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_347821"><div><strong>Charcot-Marie-Tooth disease type 4A</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>347821</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.">C1859198</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">GDAP1-related hereditary motor and sensory neuropathy (GDAP1-HMSN) is a peripheral neuropathy (also known as a subtype of Charcot-Marie-Tooth disease) that typically affects the lower extremities earlier and more severely than the upper extremities. As the neuropathy progresses, the distal upper extremities also become severely affected. Proximal muscles can also become weak. Age at onset ranges from infancy to early childhood. In most cases, disease progression causes disabilities within the first or second decade of life. At the end of the second decade, most individuals are wheelchair bound. Disease progression varies considerably even within the same family. The neuropathy can be either of the demyelinating type with reduced nerve conduction velocities or the axonal type with normal nerve conduction velocities. Vocal cord paresis is common. Intelligence is normal. Life expectancy is usually normal, but on occasion may be reduced because of secondary complications.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/347821">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_124377" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Charcot-Marie-Tooth disease type 1B</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75728" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Charcot-Marie-Tooth disease type 1C</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_347821" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Charcot-Marie-Tooth disease type 4A</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75727" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Charcot-Marie-Tooth disease, type IA</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_3710" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Dejerine-Sottas disease</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_64430" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Roussy-Lévy syndrome</a></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/35061135">Nerve ultrasound may help predicting response to immune treatment in chronic inflammatory demyelinating polyradiculoneuropathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Niu J,
|
||
Zhang L,
|
||
Fan J,
|
||
Liu J,
|
||
Ding Q,
|
||
Guan Y,
|
||
Wu S,
|
||
Cui L,
|
||
Liu M</span><br />
|
||
<span class="medgenPMjournal">Neurol Sci</span>
|
||
2022 Jun;43(6):3929-3937.
|
||
Epub 2022 Jan 21
|
||
doi: 10.1007/s10072-022-05882-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35061135" target="_blank">35061135</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33101766">Palatal Tremor - Pathophysiology, Clinical Features, Investigations, Management and Future Challenges.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bhattacharjee S</span><br />
|
||
<span class="medgenPMjournal">Tremor Other Hyperkinet Mov (N Y)</span>
|
||
2020 Oct 8;10:40.
|
||
doi: 10.5334/tohm.188.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33101766" target="_blank">33101766</a><a href="/pmc/articles/PMC7546106" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22079126">Evaluation of surgical treatment in mandibular condyle fractures.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vesnaver A,
|
||
Ahčan U,
|
||
Rozman J</span><br />
|
||
<span class="medgenPMjournal">J Craniomaxillofac Surg</span>
|
||
2012 Dec;40(8):647-53.
|
||
Epub 2011 Nov 12
|
||
doi: 10.1016/j.jcms.2011.10.029.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22079126" target="_blank">22079126</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(hypertrophic%20nerve%20changes)%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 (7)</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/36543582">ROSAH syndrome mimicking chronic uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fardeau C,
|
||
Alafaleq M,
|
||
Dhaenens CM,
|
||
Dollfus H,
|
||
Koné-Paut I,
|
||
Grunewald O,
|
||
Morel JB,
|
||
Titah C,
|
||
Saadoun D,
|
||
Lazeran PO,
|
||
Meunier I</span><br />
|
||
<span class="medgenPMjournal">Clin Genet</span>
|
||
2023 Apr;103(4):453-458.
|
||
Epub 2022 Dec 30
|
||
doi: 10.1111/cge.14286.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36543582" target="_blank">36543582</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35348828">Male Lower Extremity Sculpting.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Monarca C,
|
||
Alessi M,
|
||
Rizzo MI</span><br />
|
||
<span class="medgenPMjournal">Aesthetic Plast Surg</span>
|
||
2022 Oct;46(5):2342-2347.
|
||
Epub 2022 Mar 28
|
||
doi: 10.1007/s00266-022-02823-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35348828" target="_blank">35348828</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19917336">The role of renal sympathetic nerves in hypertension: has percutaneous renal denervation refocused attention on their clinical significance?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Katholi RE,
|
||
Rocha-Singh KJ</span><br />
|
||
<span class="medgenPMjournal">Prog Cardiovasc Dis</span>
|
||
2009 Nov-Dec;52(3):243-8.
|
||
doi: 10.1016/j.pcad.2009.09.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19917336" target="_blank">19917336</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12563417">Role of laminin bioavailability in the astroglial permissivity for neuritic outgrowth.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tardy M</span><br />
|
||
<span class="medgenPMjournal">An Acad Bras Cienc</span>
|
||
2002 Dec;74(4):683-90.
|
||
Epub 2003 Jan 24
|
||
doi: 10.1590/s0001-37652002000400009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12563417" target="_blank">12563417</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8829265">The aging glomerulus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Baylis C,
|
||
Schmidt R</span><br />
|
||
<span class="medgenPMjournal">Semin Nephrol</span>
|
||
1996 Jul;16(4):265-76.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8829265" target="_blank">8829265</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypertrophic%20nerve%20changes%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 (142)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36070242">Traumatic injury to peripheral nerves.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Robinson LR</span><br />
|
||
<span class="medgenPMjournal">Muscle Nerve</span>
|
||
2022 Dec;66(6):661-670.
|
||
Epub 2022 Sep 7
|
||
doi: 10.1002/mus.27706.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36070242" target="_blank">36070242</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34098726">HINT1 (Histidine Triad Nucleotide-Binding Protein 1) Attenuates Cardiac Hypertrophy Via Suppressing HOXA5 (Homeobox A5) Expression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhang Y,
|
||
Da Q,
|
||
Cao S,
|
||
Yan K,
|
||
Shi Z,
|
||
Miao Q,
|
||
Li C,
|
||
Hu L,
|
||
Sun S,
|
||
Wu W,
|
||
Wu L,
|
||
Chen F,
|
||
Wang L,
|
||
Gao Y,
|
||
Huang Z,
|
||
Shao Y,
|
||
Chen H,
|
||
Wei Y,
|
||
Chen F,
|
||
Han Y,
|
||
Xie L,
|
||
Ji Y</span><br />
|
||
<span class="medgenPMjournal">Circulation</span>
|
||
2021 Aug 24;144(8):638-654.
|
||
Epub 2021 Jun 8
|
||
doi: 10.1161/CIRCULATIONAHA.120.051094.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34098726" target="_blank">34098726</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33308584">Minimally Invasive Treatment for Degenerative Lumbar Spine.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nguyen KML,
|
||
Nguyen DTD</span><br />
|
||
<span class="medgenPMjournal">Tech Vasc Interv Radiol</span>
|
||
2020 Dec;23(4):100700.
|
||
Epub 2020 Oct 5
|
||
doi: 10.1016/j.tvir.2020.100700.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33308584" target="_blank">33308584</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23792284">Glia and pain: is chronic pain a gliopathy?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ji RR,
|
||
Berta T,
|
||
Nedergaard M</span><br />
|
||
<span class="medgenPMjournal">Pain</span>
|
||
2013 Dec;154 Suppl 1(0 1):S10-S28.
|
||
Epub 2013 Jun 20
|
||
doi: 10.1016/j.pain.2013.06.022.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23792284" target="_blank">23792284</a><a href="/pmc/articles/PMC3858488" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17385355">Piriformis muscle syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kuncewicz E,
|
||
Gajewska E,
|
||
Sobieska M,
|
||
Samborski W</span><br />
|
||
<span class="medgenPMjournal">Ann Acad Med Stetin</span>
|
||
2006;52(3):99-101; discussion 101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17385355" target="_blank">17385355</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypertrophic%20nerve%20changes%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 (148)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33308584">Minimally Invasive Treatment for Degenerative Lumbar Spine.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nguyen KML,
|
||
Nguyen DTD</span><br />
|
||
<span class="medgenPMjournal">Tech Vasc Interv Radiol</span>
|
||
2020 Dec;23(4):100700.
|
||
Epub 2020 Oct 5
|
||
doi: 10.1016/j.tvir.2020.100700.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33308584" target="_blank">33308584</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26232292">Fabry's disease: an example of cardiorenal syndrome type 5.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sharma A,
|
||
Sartori M,
|
||
Zaragoza JJ,
|
||
Villa G,
|
||
Lu R,
|
||
Faggiana E,
|
||
Brocca A,
|
||
Di Lullo L,
|
||
Feriozzi S,
|
||
Ronco C</span><br />
|
||
<span class="medgenPMjournal">Heart Fail Rev</span>
|
||
2015 Nov;20(6):689-708.
|
||
doi: 10.1007/s10741-015-9500-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26232292" target="_blank">26232292</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24644008">Renal denervation and heart failure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Böhm M,
|
||
Ewen S,
|
||
Kindermann I,
|
||
Linz D,
|
||
Ukena C,
|
||
Mahfoud F</span><br />
|
||
<span class="medgenPMjournal">Eur J Heart Fail</span>
|
||
2014 Jun;16(6):608-13.
|
||
Epub 2014 Mar 18
|
||
doi: 10.1002/ejhf.83.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24644008" target="_blank">24644008</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24022031">Statins in heart failure--With preserved and reduced ejection fraction. An update.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tousoulis D,
|
||
Oikonomou E,
|
||
Siasos G,
|
||
Stefanadis C</span><br />
|
||
<span class="medgenPMjournal">Pharmacol Ther</span>
|
||
2014 Jan;141(1):79-91.
|
||
Epub 2013 Sep 8
|
||
doi: 10.1016/j.pharmthera.2013.09.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24022031" target="_blank">24022031</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9276166">The power athlete.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Longhurst JC,
|
||
Stebbins CL</span><br />
|
||
<span class="medgenPMjournal">Cardiol Clin</span>
|
||
1997 Aug;15(3):413-29.
|
||
doi: 10.1016/s0733-8651(05)70349-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9276166" target="_blank">9276166</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypertrophic%20nerve%20changes%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 (79)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36543582">ROSAH syndrome mimicking chronic uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fardeau C,
|
||
Alafaleq M,
|
||
Dhaenens CM,
|
||
Dollfus H,
|
||
Koné-Paut I,
|
||
Grunewald O,
|
||
Morel JB,
|
||
Titah C,
|
||
Saadoun D,
|
||
Lazeran PO,
|
||
Meunier I</span><br />
|
||
<span class="medgenPMjournal">Clin Genet</span>
|
||
2023 Apr;103(4):453-458.
|
||
Epub 2022 Dec 30
|
||
doi: 10.1111/cge.14286.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36543582" target="_blank">36543582</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36070242">Traumatic injury to peripheral nerves.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Robinson LR</span><br />
|
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<span class="medgenPMjournal">Muscle Nerve</span>
|
||
2022 Dec;66(6):661-670.
|
||
Epub 2022 Sep 7
|
||
doi: 10.1002/mus.27706.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36070242" target="_blank">36070242</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29382617">Hypertrophic Olivary Degeneration: Neurosurgical Perspective and Literature Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Onen MR,
|
||
Moore K,
|
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Cikla U,
|
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Ucer M,
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Schmidt B,
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2018 Apr;112:e763-e771.
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Epub 2018 Jan 31
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doi: 10.1016/j.wneu.2018.01.150.
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<span class="bold">PMID: </span><a href="/pubmed/29382617" target="_blank">29382617</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3530120">Familial myoclonic dementia masquerading as Creutzfeldt-Jakob disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Little BW,
|
||
Brown PW,
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Rodgers-Johnson P,
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Perl DP,
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Gajdusek DC</span><br />
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<span class="medgenPMjournal">Ann Neurol</span>
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1986 Aug;20(2):231-9.
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doi: 10.1002/ana.410200209.
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<span class="bold">PMID: </span><a href="/pubmed/3530120" target="_blank">3530120</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1186294">Chronic inflammatory polyradiculoneuropathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dyck PJ,
|
||
Lais AC,
|
||
Ohta M,
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Bastron JA,
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Okazaki H,
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Groover RV</span><br />
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<span class="medgenPMjournal">Mayo Clin Proc</span>
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1975 Nov;50(11):621-37.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1186294" target="_blank">1186294</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypertrophic%20nerve%20changes%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 (66)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35348828">Male Lower Extremity Sculpting.</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Monarca C,
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Alessi M,
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Rizzo MI</span><br />
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<span class="medgenPMjournal">Aesthetic Plast Surg</span>
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2022 Oct;46(5):2342-2347.
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Epub 2022 Mar 28
|
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doi: 10.1007/s00266-022-02823-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35348828" target="_blank">35348828</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34098726">HINT1 (Histidine Triad Nucleotide-Binding Protein 1) Attenuates Cardiac Hypertrophy Via Suppressing HOXA5 (Homeobox A5) Expression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhang Y,
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Da Q,
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Cao S,
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Yan K,
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Shi Z,
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Miao Q,
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Li C,
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Hu L,
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Sun S,
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||
Wu W,
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Wu L,
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Chen F,
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Wang L,
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Gao Y,
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||
Huang Z,
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Shao Y,
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Chen H,
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Wei Y,
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Chen F,
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Han Y,
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Xie L,
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Ji Y</span><br />
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<span class="medgenPMjournal">Circulation</span>
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2021 Aug 24;144(8):638-654.
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Epub 2021 Jun 8
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doi: 10.1161/CIRCULATIONAHA.120.051094.
|
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<span class="bold">PMID: </span><a href="/pubmed/34098726" target="_blank">34098726</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/31588577">Thigh muscle MRI findings in myopathy associated with anti-mitochondrial antibody.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Minamiyama S,
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Ueda S,
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Nakashima R,
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Yamakado H,
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Sakato Y,
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Yamashita H,
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Sawamoto N,
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Fujimoto R,
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Nishino I,
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Urushitani M,
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Mimori T,
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Takahashi R</span><br />
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<span class="medgenPMjournal">Muscle Nerve</span>
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2020 Jan;61(1):81-87.
|
||
Epub 2019 Nov 8
|
||
doi: 10.1002/mus.26731.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31588577" target="_blank">31588577</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25771924">Hypertrophic pachymeningitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dziedzic T,
|
||
Wojciechowski J,
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||
Nowak A,
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Marchel A</span><br />
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<span class="medgenPMjournal">Childs Nerv Syst</span>
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||
2015 Jul;31(7):1025-31.
|
||
Epub 2015 Mar 15
|
||
doi: 10.1007/s00381-015-2680-z.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25771924" target="_blank">25771924</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12563417">Role of laminin bioavailability in the astroglial permissivity for neuritic outgrowth.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tardy M</span><br />
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<span class="medgenPMjournal">An Acad Bras Cienc</span>
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2002 Dec;74(4):683-90.
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Epub 2003 Jan 24
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||
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|
||
<span class="bold">PMID: </span><a href="/pubmed/12563417" target="_blank">12563417</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypertrophic%20nerve%20changes%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 (155)</a></div></div>
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|
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|
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<div class="nl"><a target="_blank" href="/pubmed/34284162">Clinical Features, Natural History, and Outcomes of Intraneural Perineuriomas: A Systematic Review of the Literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lenartowicz KA,
|
||
Goyal A,
|
||
Mauermann ML,
|
||
Wilson TJ,
|
||
Spinner RJ</span><br />
|
||
<span class="medgenPMjournal">World Neurosurg</span>
|
||
2021 Oct;154:120-131.e8.
|
||
Epub 2021 Jul 17
|
||
doi: 10.1016/j.wneu.2021.07.042.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34284162" target="_blank">34284162</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32281018">Lumbar disc herniation with contralateral radiculopathy: a systematic review on pathophysiology and surgical strategies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ruschel LG,
|
||
Agnoletto GJ,
|
||
Aragão A,
|
||
Duarte JS,
|
||
de Oliveira MF,
|
||
Teles AR</span><br />
|
||
<span class="medgenPMjournal">Neurosurg Rev</span>
|
||
2021 Apr;44(2):1071-1081.
|
||
Epub 2020 Apr 13
|
||
doi: 10.1007/s10143-020-01294-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32281018" target="_blank">32281018</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30562201">Donor Site Morbidities of Iliac Crest Bone Graft in Craniofacial Surgery: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Boehm KS,
|
||
Al-Taha M,
|
||
Morzycki A,
|
||
Samargandi OA,
|
||
Al-Youha S,
|
||
LeBlanc MR</span><br />
|
||
<span class="medgenPMjournal">Ann Plast Surg</span>
|
||
2019 Sep;83(3):352-358.
|
||
doi: 10.1097/SAP.0000000000001682.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30562201" target="_blank">30562201</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27634052">A systematic review of prenatal screening for congenital heart disease by fetal electrocardiography.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Verdurmen KM,
|
||
Eijsvoogel NB,
|
||
Lempersz C,
|
||
Vullings R,
|
||
Schroer C,
|
||
van Laar JO,
|
||
Oei SG</span><br />
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||
<span class="medgenPMjournal">Int J Gynaecol Obstet</span>
|
||
2016 Nov;135(2):129-134.
|
||
Epub 2016 Aug 4
|
||
doi: 10.1016/j.ijgo.2016.05.010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27634052" target="_blank">27634052</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypertrophic%20nerve%20changes%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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<li>
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<a class="text-white" href="https://www.usa.gov/">USA.gov</a>
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