Crouch Gait in Dravet Syndrome

Crouch Gait in Dravet Syndrome

Investigators from Necker Enfants Malades Hospital, Sorbonne Paris Cite University, Raymond Poincare University, and Paris Descartes University studied motor neuron function in children with Dravet syndrome (DS).

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Laura Black, Deborah Gaebler-Spira
التنسيق:	مقال
اللغة:	English
منشور في:	Pediatric Neurology Briefs Publishers 2016-11-01
سلاسل:	Pediatric Neurology Briefs
الموضوعات:	dravet syndrome neurologic gait disorders nav1.1 voltage gated sodium channel
الوصول للمادة أونلاين:	https://www.pediatricneurologybriefs.com/articles/3790

مواد مشابهة

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A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients
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Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulated pathways for chromatin remodeling and neurodevelopment
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Generation and Characterization of the <i>Drosophila melanogaster paralytic</i> Gene Knock-Out as a Model for Dravet Syndrome
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The Generation of Human iPSC Lines from Three Individuals with Dravet Syndrome and Characterization of Neural Differentiation Markers in iPSC-Derived Ventral Forebrain Organoid Model
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The Tarantula Venom Peptide Eo1a Binds to the Domain II S3-S4 Extracellular Loop of Voltage-Gated Sodium Channel NaV1.8 to Enhance Activation
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Role of the hippocampus in Nav1.6 (Scn8a) mediated seizure resistance
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Extremely Potent Block of Bacterial Voltage-Gated Sodium Channels by µ-Conotoxin PIIIA
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Genetic and Functional Differences between Duplicated Zebrafish Genes for Human <i>SCN1A</i>
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Effects of Mexiletine on a Race-specific Mutation in Nav1.5 Associated With Long QT Syndrome
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Dataset of electrophysiological patch-clamp recordings of the effect of the compounds deltamethrin, ATx-II and β4-peptide on human cardiac Nav1.5 sodium channel gating properties
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Molecular determinants of μ-conotoxin KIIIA interaction with the human voltage-gated sodium channel NaV1.7
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Vaccinations and Dravet Syndrome
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Animal Toxins Can Alter the Function of Nav1.8 and Nav1.9
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