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<!--
|
||
UID=488958
|
||
ConceptID=C1279412
|
||
-->
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||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Periodic paralysis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>488958</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.">C1279412</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Episodic paralysis</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Periodic paralysis (198030008)</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:0003768">HP:0003768</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0016122" target="_blank">MONDO:0016122</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=206976">ORPHA206976</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">Episodes of muscle weakness. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1279412[DISCUI]&test_type=Clinical&redirect=true" ref="ncbi_uid=488958">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 Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=488958" ref="ncbi_uid=488958">V</a></span></span><span class="TLline">Periodic paralysis</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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/868417" ref="tree=MeSH" title="MedGen record for Abnormal nervous system physiology">Abnormal nervous system physiology</a></span><ul><li><span class="TLline"><a href="/medgen/868940" ref="tree=MeSH" title="MedGen record for Abnormal central motor function">Abnormal central motor function</a></span><ul><li><span class="TLline"><a href="/medgen/105510" ref="tree=MeSH" title="MedGen record for Paralysis">Paralysis</a></span><ul><li><span class="matched_ds">Periodic paralysis</span><ul><li><span class="TLline"><a href="/medgen/327586" ref="tree=MeSH" title="MedGen record for Andersen Tawil syndrome">Andersen Tawil syndrome</a></span></li><li><span class="TLline"><a href="/medgen/68665" ref="tree=MeSH" title="MedGen record for Hyperkalemic periodic paralysis">Hyperkalemic periodic paralysis</a></span></li><li><span class="TLline"><a href="/medgen/116058" ref="tree=MeSH" title="MedGen record for Hypokalemic periodic paralysis">Hypokalemic periodic paralysis</a></span><ul><li><span class="TLline"><a href="/medgen/811387" ref="tree=MeSH" title="MedGen record for Hypokalemic periodic paralysis, type 1">Hypokalemic periodic paralysis, type 1</a></span></li><li><span class="TLline"><a href="/medgen/413748" ref="tree=MeSH" title="MedGen record for Hypokalemic periodic paralysis, type 2">Hypokalemic periodic paralysis, type 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/867195" ref="tree=MeSH" title="MedGen record for Periodic hypokalemic paresis">Periodic hypokalemic paresis</a></span></li><li><span class="TLline"><a href="/medgen/1670241" ref="tree=MeSH" title="MedGen record for Periodic paralysis with later-onset distal motor neuropathy">Periodic paralysis with later-onset distal motor neuropathy</a></span></li><li><span class="TLline"><a href="/medgen/1668303" ref="tree=MeSH" title="MedGen record for Periodic paralysis with transient compartment-like syndrome">Periodic paralysis with transient compartment-like syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120639" ref="tree=MeSH" title="MedGen record for Thyrotoxic periodic paralysis">Thyrotoxic periodic paralysis</a></span></li></ul></li></ul></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_75688"><div><strong>Tyrosinemia type I</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75688</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.">C0268490</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Untreated tyrosinemia type I usually presents either in young infants with severe liver involvement or later in the first year with liver dysfunction and renal tubular dysfunction associated with growth failure and rickets. Untreated children may have repeated, often unrecognized, neurologic crises lasting one to seven days that can include change in mental status, abdominal pain, peripheral neuropathy, and/or respiratory failure requiring mechanical ventilation. Death in the untreated child usually occurs before age ten years, typically from liver failure, neurologic crisis, or hepatocellular carcinoma. Combined treatment with nitisinone and a low-tyrosine diet has resulted in a greater than 90% survival rate, normal growth, improved liver function, prevention of cirrhosis, correction of renal tubular acidosis, and improvement in secondary rickets.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75688">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_327586"><div><strong>Andersen Tawil syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>327586</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.">C1563715</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Andersen-Tawil syndrome (ATS) is characterized by a triad of: episodic flaccid muscle weakness (i.e., periodic paralysis); ventricular arrhythmias and prolonged QT interval; and anomalies including low-set ears, widely spaced eyes, small mandible, fifth-digit clinodactyly, syndactyly, short stature, and scoliosis. Affected individuals present in the first or second decade with either cardiac symptoms (palpitations and/or syncope) or weakness that occurs spontaneously following prolonged rest or following rest after exertion. Mild permanent weakness is common. Mild learning difficulties and a distinct neurocognitive phenotype (i.e., deficits in executive function and abstract reasoning) have been described.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/327586">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_324588"><div><strong>Familial pseudohyperkalemia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>324588</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.">C1836705</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">'Familial pseudohyperkalemia' (PSHK) is a term that was coined to describe conditions in which a patient presents with pseudohyperkalemia as a result of a temperature-based abnormality in the transport of potassium (K) and sodium (Na) across the red cell membrane, in association with essentially normal hematology. PSHK can be considered to be the clinically benign, nonhemolytic cousin of hereditary stomatocytic leaky-cell, congenital hemolytic anemias (see 194380) (summary by Gore et al., 2002). For a discussion of clinical and genetic heterogeneity of the hereditary stomatocytoses, see 194380.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/324588">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_336601"><div><strong>Renal tubular acidosis 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>336601</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.">C1849435</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/336601">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_413199"><div><strong>Thyrotoxic periodic paralysis, susceptibility to, 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>413199</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.">C2749982</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Thyrotoxic periodic paralysis is a sporadic muscle disorder characterized by episodic attacks of weakness associated with hypokalemia in individuals with hyperthyroidism. The paralysis resolves upon treatment of hyperthyroidism. The disorder is most common among males of Asian descent, including Chinese, Japanese, Vietnamese, Filipino, and Koreans, although it occurs less commonly in individuals of Caucasian background. Thyrotoxic periodic paralysis is clinically similar to hereditary hypokalemic periodic paralysis (HOKPP; 170400), but the paralysis in TTPP occurs only in the presence of hyperthyroidism. TTPP can also be precipitated by factors that result in hypokalemia, such as carbohydrate ingestion and rest after exercise (review by Kung, 2006). Genetic Heterogeneity of Thyrotoxic Periodic Paralysis See also TTPP2 (613239), conferred by variation in the KCNJ18 gene (613236) on chromosome 17p11, and TTPP3 (614834), mapped to chromosome 17q24.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/413199">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_413748"><div><strong>Hypokalemic periodic paralysis, type 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>413748</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.">C2750061</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypokalemic periodic paralysis (hypoPP) is a condition in which affected individuals may experience paralytic episodes with concomitant hypokalemia (serum potassium <3.5 mmol/L). The paralytic attacks are characterized by decreased muscle tone (flaccidity) more marked proximally than distally with normal to decreased deep tendon reflexes. The episodes develop over minutes to hours and last several minutes to several days with spontaneous recovery. Some individuals have only one episode in a lifetime; more commonly, crises occur repeatedly: daily, weekly, monthly, or less often. The major triggering factors are cessation of effort following strenuous exercise and carbohydrate-rich evening meals. Additional triggers can include cold, stress/excitement/fear, salt intake, prolonged immobility, use of glucosteroids or alcohol, and anesthetic procedures. The age of onset of the first attack ranges from two to 30 years; the duration of paralytic episodes ranges from one to 72 hours with an average of nearly 24 hours. Long-lasting interictal muscle weakness may occur in some affected individuals and in some stages of the disease and in myopathic muscle changes. A myopathy may occur independent of paralytic symptoms and may be the sole manifestation of hypoPP.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/413748">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_413851"><div><strong>Thyrotoxic periodic paralysis, susceptibility to, 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>413851</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.">C2750473</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any thyrotoxic periodic paralysis in which the cause of the disease is a mutation in the KCNJ18 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/413851">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_481742"><div><strong>Congenital myasthenic syndrome 16</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>481742</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.">C3280112</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Congenital myasthenic syndrome is a disorder characterized by variable degrees of muscle fatigability caused by impaired transmission of electrical signals at the neuromuscular junction (NMJ) (summary by Arnold et al., 2015). For a discussion of genetic heterogeneity of CMS, see CMS1A (601462).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/481742">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_811387"><div><strong>Hypokalemic periodic paralysis, type 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>811387</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.">C3714580</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypokalemic periodic paralysis (hypoPP) is a condition in which affected individuals may experience paralytic episodes with concomitant hypokalemia (serum potassium <3.5 mmol/L). The paralytic attacks are characterized by decreased muscle tone (flaccidity) more marked proximally than distally with normal to decreased deep tendon reflexes. The episodes develop over minutes to hours and last several minutes to several days with spontaneous recovery. Some individuals have only one episode in a lifetime; more commonly, crises occur repeatedly: daily, weekly, monthly, or less often. The major triggering factors are cessation of effort following strenuous exercise and carbohydrate-rich evening meals. Additional triggers can include cold, stress/excitement/fear, salt intake, prolonged immobility, use of glucosteroids or alcohol, and anesthetic procedures. The age of onset of the first attack ranges from two to 30 years; the duration of paralytic episodes ranges from one to 72 hours with an average of nearly 24 hours. Long-lasting interictal muscle weakness may occur in some affected individuals and in some stages of the disease and in myopathic muscle changes. A myopathy may occur independent of paralytic symptoms and may be the sole manifestation of hypoPP.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/811387">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_327586" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Andersen Tawil syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_481742" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital myasthenic syndrome 16</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_324588" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Familial pseudohyperkalemia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_811387" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypokalemic periodic paralysis, type 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_413748" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypokalemic periodic paralysis, type 2</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_336601" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Renal tubular acidosis 3</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_413199" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Thyrotoxic periodic paralysis, susceptibility to, 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_413851" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Thyrotoxic periodic paralysis, susceptibility to, 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75688" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Tyrosinemia type I</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/36848916">Hyperthyroidism: aetiology, pathogenesis, diagnosis, management, complications, and prognosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wiersinga WM,
|
||
Poppe KG,
|
||
Effraimidis G</span><br />
|
||
<span class="medgenPMjournal">Lancet Diabetes Endocrinol</span>
|
||
2023 Apr;11(4):282-298.
|
||
Epub 2023 Feb 24
|
||
doi: 10.1016/S2213-8587(23)00005-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36848916" target="_blank">36848916</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29125635">Review of the Diagnosis and Treatment of Periodic Paralysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Statland JM,
|
||
Fontaine B,
|
||
Hanna MG,
|
||
Johnson NE,
|
||
Kissel JT,
|
||
Sansone VA,
|
||
Shieh PB,
|
||
Tawil RN,
|
||
Trivedi J,
|
||
Cannon SC,
|
||
Griggs RC</span><br />
|
||
<span class="medgenPMjournal">Muscle Nerve</span>
|
||
2018 Apr;57(4):522-530.
|
||
Epub 2017 Nov 29
|
||
doi: 10.1002/mus.26009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29125635" target="_blank">29125635</a><a href="/pmc/articles/PMC5867231" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19377223">Diagnosis of hypokalemia: a problem-solving approach to clinical cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Assadi F</span><br />
|
||
<span class="medgenPMjournal">Iran J Kidney Dis</span>
|
||
2008 Jul;2(3):115-22.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19377223" target="_blank">19377223</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22periodic%20paralysis%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (38)</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/36848916">Hyperthyroidism: aetiology, pathogenesis, diagnosis, management, complications, and prognosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wiersinga WM,
|
||
Poppe KG,
|
||
Effraimidis G</span><br />
|
||
<span class="medgenPMjournal">Lancet Diabetes Endocrinol</span>
|
||
2023 Apr;11(4):282-298.
|
||
Epub 2023 Feb 24
|
||
doi: 10.1016/S2213-8587(23)00005-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36848916" target="_blank">36848916</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32703462">Skeletal Muscle Channelopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vivekanandam V,
|
||
Munot P,
|
||
Hanna MG,
|
||
Matthews E</span><br />
|
||
<span class="medgenPMjournal">Neurol Clin</span>
|
||
2020 Aug;38(3):481-491.
|
||
doi: 10.1016/j.ncl.2020.04.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32703462" target="_blank">32703462</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32560786">"Electrifying dysmorphology": Potassium channelopathies causing dysmorphic syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hamilton MJ,
|
||
Suri M</span><br />
|
||
<span class="medgenPMjournal">Adv Genet</span>
|
||
2020;105:137-174.
|
||
Epub 2020 May 26
|
||
doi: 10.1016/bs.adgen.2020.03.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32560786" target="_blank">32560786</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29478596">Periodic paralysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fialho D,
|
||
Griggs RC,
|
||
Matthews E</span><br />
|
||
<span class="medgenPMjournal">Handb Clin Neurol</span>
|
||
2018;148:505-520.
|
||
doi: 10.1016/B978-0-444-64076-5.00032-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29478596" target="_blank">29478596</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18351527">Muscle channelopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Saperstein DS</span><br />
|
||
<span class="medgenPMjournal">Semin Neurol</span>
|
||
2008 Apr;28(2):260-9.
|
||
doi: 10.1055/s-2008-1062262.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18351527" target="_blank">18351527</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periodic%20paralysis%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 (243)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37562884">Muscle channelopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vivekanandam V,
|
||
Jayaseelan D,
|
||
Hanna MG</span><br />
|
||
<span class="medgenPMjournal">Handb Clin Neurol</span>
|
||
2023;195:521-532.
|
||
doi: 10.1016/B978-0-323-98818-6.00006-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37562884" target="_blank">37562884</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33983691">Thyrotoxic Periodic Paralysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fralick M,
|
||
Sarma S</span><br />
|
||
<span class="medgenPMjournal">N Engl J Med</span>
|
||
2021 May 13;384(19):e71.
|
||
Epub 2021 May 8
|
||
doi: 10.1056/NEJMicm2030770.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33983691" target="_blank">33983691</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29125635">Review of the Diagnosis and Treatment of Periodic Paralysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Statland JM,
|
||
Fontaine B,
|
||
Hanna MG,
|
||
Johnson NE,
|
||
Kissel JT,
|
||
Sansone VA,
|
||
Shieh PB,
|
||
Tawil RN,
|
||
Trivedi J,
|
||
Cannon SC,
|
||
Griggs RC</span><br />
|
||
<span class="medgenPMjournal">Muscle Nerve</span>
|
||
2018 Apr;57(4):522-530.
|
||
Epub 2017 Nov 29
|
||
doi: 10.1002/mus.26009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29125635" target="_blank">29125635</a><a href="/pmc/articles/PMC5867231" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27741989">Acute Generalized Weakness.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ganti L,
|
||
Rastogi V</span><br />
|
||
<span class="medgenPMjournal">Emerg Med Clin North Am</span>
|
||
2016 Nov;34(4):795-809.
|
||
Epub 2016 Sep 3
|
||
doi: 10.1016/j.emc.2016.06.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27741989" target="_blank">27741989</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18351527">Muscle channelopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Saperstein DS</span><br />
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<span class="medgenPMjournal">Semin Neurol</span>
|
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2008 Apr;28(2):260-9.
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doi: 10.1055/s-2008-1062262.
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<span class="bold">PMID: </span><a href="/pubmed/18351527" target="_blank">18351527</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periodic%20paralysis%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 (690)</a></div><h3 class="subhead">Therapy</h3>
|
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<div class="nl"><a target="_blank" href="/pubmed/36848916">Hyperthyroidism: aetiology, pathogenesis, diagnosis, management, complications, and prognosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wiersinga WM,
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Poppe KG,
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Effraimidis G</span><br />
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<span class="medgenPMjournal">Lancet Diabetes Endocrinol</span>
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2023 Apr;11(4):282-298.
|
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Epub 2023 Feb 24
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doi: 10.1016/S2213-8587(23)00005-0.
|
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<span class="bold">PMID: </span><a href="/pubmed/36848916" target="_blank">36848916</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/36537980">Muscle Channelopathies.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Trivedi JR</span><br />
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<span class="medgenPMjournal">Continuum (Minneap Minn)</span>
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<div class="nl"><a target="_blank" href="/pubmed/33983691">Thyrotoxic Periodic Paralysis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Fralick M,
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<span class="medgenPMjournal">N Engl J Med</span>
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2021 May 13;384(19):e71.
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Epub 2021 May 8
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<span class="bold">PMID: </span><a href="/pubmed/33983691" target="_blank">33983691</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/30169664">Thyrotoxic hypokalemic periodic paralysis.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Urbina-Soto L,
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Hernández-Martínez P,
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Ortiz-Flores F,
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2018 Dec 1;111(12):887-889.
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<span class="bold">PMID: </span><a href="/pubmed/30169664" target="_blank">30169664</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/29125635">Review of the Diagnosis and Treatment of Periodic Paralysis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Statland JM,
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Fontaine B,
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Hanna MG,
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Johnson NE,
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Kissel JT,
|
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Sansone VA,
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Shieh PB,
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Tawil RN,
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Trivedi J,
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<span class="medgenPMjournal">Muscle Nerve</span>
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2018 Apr;57(4):522-530.
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Epub 2017 Nov 29
|
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doi: 10.1002/mus.26009.
|
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<span class="bold">PMID: </span><a href="/pubmed/29125635" target="_blank">29125635</a><a href="/pmc/articles/PMC5867231" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periodic%20paralysis%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 (435)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36848916">Hyperthyroidism: aetiology, pathogenesis, diagnosis, management, complications, and prognosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wiersinga WM,
|
||
Poppe KG,
|
||
Effraimidis G</span><br />
|
||
<span class="medgenPMjournal">Lancet Diabetes Endocrinol</span>
|
||
2023 Apr;11(4):282-298.
|
||
Epub 2023 Feb 24
|
||
doi: 10.1016/S2213-8587(23)00005-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36848916" target="_blank">36848916</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35119093">Thyrotoxic myopathy: research status, diagnosis, and treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cui H,
|
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Zhang X</span><br />
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<span class="medgenPMjournal">Endokrynol Pol</span>
|
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2022;73(1):157-162.
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Epub 2022 Feb 4
|
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doi: 10.5603/EP.a2022.0004.
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<span class="bold">PMID: </span><a href="/pubmed/35119093" target="_blank">35119093</a></div>
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|
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<div class="nl"><a target="_blank" href="/pubmed/32947483">Andersen-Tawil Syndrome: A Comprehensive Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pérez-Riera AR,
|
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Barbosa-Barros R,
|
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Samesina N,
|
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Pastore CA,
|
||
Scanavacca M,
|
||
Daminello-Raimundo R,
|
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de Abreu LC,
|
||
Nikus K,
|
||
Brugada P</span><br />
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<span class="medgenPMjournal">Cardiol Rev</span>
|
||
2021 Jul-Aug 01;29(4):165-177.
|
||
doi: 10.1097/CRD.0000000000000326.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32947483" target="_blank">32947483</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32077432">Management of Conn's Syndrome Associated with Hypokalemic Nonperiodic Paralysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Elson MJ,
|
||
Wang VL,
|
||
Sharma J</span><br />
|
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<span class="medgenPMjournal">Am Surg</span>
|
||
2020 Jan 1;86(1):e33-e34.
|
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<span class="bold">PMID: </span><a href="/pubmed/32077432" target="_blank">32077432</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12420087">Skeletal muscle channelopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jurkat-Rott K,
|
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Lerche H,
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Lehmann-Horn F</span><br />
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<span class="medgenPMjournal">J Neurol</span>
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2002 Nov;249(11):1493-502.
|
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doi: 10.1007/s00415-002-0871-5.
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<span class="bold">PMID: </span><a href="/pubmed/12420087" target="_blank">12420087</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periodic%20paralysis%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 (135)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32947483">Andersen-Tawil Syndrome: A Comprehensive Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pérez-Riera AR,
|
||
Barbosa-Barros R,
|
||
Samesina N,
|
||
Pastore CA,
|
||
Scanavacca M,
|
||
Daminello-Raimundo R,
|
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de Abreu LC,
|
||
Nikus K,
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Brugada P</span><br />
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<span class="medgenPMjournal">Cardiol Rev</span>
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2021 Jul-Aug 01;29(4):165-177.
|
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doi: 10.1097/CRD.0000000000000326.
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<span class="bold">PMID: </span><a href="/pubmed/32947483" target="_blank">32947483</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32657178">Improving genetic diagnostics of skeletal muscle channelopathies.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Vivekanandam V,
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Männikkö R,
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Matthews E,
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Hanna MG</span><br />
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<span class="medgenPMjournal">Expert Rev Mol Diagn</span>
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2020 Jul;20(7):725-736.
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Epub 2020 Jul 12
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doi: 10.1080/14737159.2020.1782195.
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||
<span class="bold">PMID: </span><a href="/pubmed/32657178" target="_blank">32657178</a></div>
|
||
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<div class="nl"><a target="_blank" href="/pubmed/28561926">Quantitative sonographic assessment of myotonia.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Abraham A,
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Breiner A,
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Barnett C,
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Bril V,
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Katzberg HD</span><br />
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<span class="medgenPMjournal">Muscle Nerve</span>
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||
2018 Jan;57(1):146-149.
|
||
Epub 2017 Jul 31
|
||
doi: 10.1002/mus.25714.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28561926" target="_blank">28561926</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12420087">Skeletal muscle channelopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jurkat-Rott K,
|
||
Lerche H,
|
||
Lehmann-Horn F</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2002 Nov;249(11):1493-502.
|
||
doi: 10.1007/s00415-002-0871-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12420087" target="_blank">12420087</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10369304">Genetic linkage analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pulst SM</span><br />
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<span class="medgenPMjournal">Arch Neurol</span>
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1999 Jun;56(6):667-72.
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||
doi: 10.1001/archneur.56.6.667.
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||
<span class="bold">PMID: </span><a href="/pubmed/10369304" target="_blank">10369304</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periodic%20paralysis%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 (197)</a></div></div>
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|
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|
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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/33325393">Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision Medicine.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Desaphy JF,
|
||
Altamura C,
|
||
Vicart S,
|
||
Fontaine B</span><br />
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||
<span class="medgenPMjournal">J Neuromuscul Dis</span>
|
||
2021;8(3):357-381.
|
||
doi: 10.3233/JND-200582.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33325393" target="_blank">33325393</a><a href="/pmc/articles/PMC8203248" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31439490">Secondary hypokalemic paralysis with bulbar weakness and reversible electrophysiologic abnormalities: A case report and systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ignacio KHD,
|
||
Bagnas MAC,
|
||
Espiritu AI,
|
||
Reyes JPBT</span><br />
|
||
<span class="medgenPMjournal">J Clin Neurosci</span>
|
||
2019 Dec;70:254-257.
|
||
Epub 2019 Aug 19
|
||
doi: 10.1016/j.jocn.2019.08.063.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31439490" target="_blank">31439490</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18254068">Treatment for periodic paralysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sansone V,
|
||
Meola G,
|
||
Links TP,
|
||
Panzeri M,
|
||
Rose MR</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2008 Jan 23;(1):CD005045.
|
||
doi: 10.1002/14651858.CD005045.pub2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18254068" target="_blank">18254068</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periodic%20paralysis%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 (3)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C1279412%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (1)</a></li>
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<li><a href="/gtr/tests?term=C1279412%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (1)</a></li>
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<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C1279412%5bDISCUI%5d" target="_blank">See all (1)</a></total></li>
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