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).

书目详细资料
Main Authors:	Laura Black, Deborah Gaebler-Spira
格式:	文件
语言:	English
出版:	Pediatric Neurology Briefs Publishers 2016-11-01
丛编:	Pediatric Neurology Briefs
主题:	dravet syndrome neurologic gait disorders nav1.1 voltage gated sodium channel
在线阅读:	https://www.pediatricneurologybriefs.com/articles/3790

相似书籍

Functional Investigation of a Neuronal Microcircuit in the CA1 Area of the Hippocampus Reveals Synaptic Dysfunction in Dravet Syndrome Mice
由: Yael Almog, et al.
出版: (2022-03-01)

Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome
由: Moran Rubinstein, et al.
出版: (2015-01-01)

Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome
由: Joanna Mattis, et al.
出版: (2022-02-01)

Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations
由: Lucia Mora-Jimenez, et al.
出版: (2021-09-01)

Phenotypes of Dravet Syndrome
由: Rebecca Garcia-Sosa, et al.
出版: (2016-08-01)

A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients
由: Yishan Sun, et al.
出版: (2016-07-01)

Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulated pathways for chromatin remodeling and neurodevelopment
由: Jens Schuster, et al.
出版: (2019-12-01)

Generation and Characterization of the <i>Drosophila melanogaster paralytic</i> Gene Knock-Out as a Model for Dravet Syndrome
由: Andrea Tapia, et al.
出版: (2021-11-01)

Mutação no gene scn1a e suas diferentes expressões fenotípicas - comparação de dois casos
由: Brenda Klemm Arci Mattos de Freitas Alves, et al.
出版: (2023-06-01)

Focal Scn1a knockdown induces cognitive impairment without seizures
由: Alex C. Bender, et al.
出版: (2013-06-01)

NaV1.1 is essential for proprioceptive signaling and motor behaviors
由: Cyrrus M Espino, et al.
出版: (2022-10-01)

Neurodevelopmental defects in Dravet syndrome Scn1a+/− mice: Targeting GABA-switch rescues behavioral dysfunctions but not seizures and mortality
由: Lara Pizzamiglio, et al.
出版: (2025-04-01)

Compromised function in the Nav1.2 Dravet syndrome mutation R1312T
由: Christoph Lossin, et al.
出版: (2012-09-01)

Cell-Adhesion Properties of β-Subunits in the Regulation of Cardiomyocyte Sodium Channels
由: Samantha C. Salvage, et al.
出版: (2020-07-01)

Dravet Variant SCN1AA1783V Impairs Interneuron Firing Predominantly by Altered Channel Activation
由: Nikolas Layer, et al.
出版: (2021-10-01)

Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet syndrome
由: Kevin M Goff, et al.
出版: (2019-07-01)

Antinociceptive effects of AGAP, a recombinant neurotoxic polypeptide: Possible involvement of the tetrodotoxin-resistant sodium channels in small dorsal root ganglia neurons
由: Li Chunli, et al.
出版: (2016-12-01)

Recent developments regarding voltage-gated sodium channel blockers for the treatment of inherited and acquired neuropathic pain syndromes
由: Jonathan W. Theile, et al.
出版: (2011-10-01)

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
由: Valery Zayat, et al.
出版: (2023-01-01)

Epileptic seizures worsen the gait and motor abnormalities in adult patients with Dravet syndrome (with a case report and literature review)
由: Xiaoping Du, et al.
出版: (2023-12-01)

Genetic Variants in the SCN9A Gene are Detected in a Minority of Erythromelalgia Patients
由: Mari Skystad Kvernebo, et al.
出版: (2025-01-01)

Insights into the voltage-gated sodium channel, NaV1.8, and its role in visceral pain perception
由: J. Westley Heinle, et al.
出版: (2024-05-01)

The Tarantula Venom Peptide Eo1a Binds to the Domain II S3-S4 Extracellular Loop of Voltage-Gated Sodium Channel NaV1.8 to Enhance Activation
由: Jennifer R. Deuis, et al.
出版: (2022-01-01)

Role of the hippocampus in Nav1.6 (Scn8a) mediated seizure resistance
由: Christopher D. Makinson, et al.
出版: (2014-08-01)

Extremely Potent Block of Bacterial Voltage-Gated Sodium Channels by µ-Conotoxin PIIIA
由: Rocio K. Finol-Urdaneta, et al.
出版: (2019-08-01)

Genetic and Functional Differences between Duplicated Zebrafish Genes for Human <i>SCN1A</i>
由: Wout J. Weuring, et al.
出版: (2022-01-01)

Effects of Mexiletine on a Race-specific Mutation in Nav1.5 Associated With Long QT Syndrome
由: Xin Wu, et al.
出版: (2022-07-01)

Patient with Dravet syndrome: A case report
由: Rukesh Yadav, et al.
出版: (2022-05-01)

Fenestropathy of Voltage-Gated Sodium Channels
由: Tamer M. Gamal El-Din, et al.
出版: (2022-02-01)

Conotoxins Targeting Neuronal Voltage-Gated Sodium Channel Subtypes: Potential Analgesics?
由: Jeffrey R. McArthur, et al.
出版: (2012-11-01)

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
由: Sarah Thull, et al.
出版: (2020-08-01)

Deficiency of autism-related Scn2a gene in mice disrupts sleep patterns and circadian rhythms
由: Zhixiong Ma, et al.
出版: (2022-06-01)

Molecular Surface of JZTX-V (β-Theraphotoxin-Cj2a) Interacting with Voltage-Gated Sodium Channel Subtype NaV1.4
由: Ji Luo, et al.
出版: (2014-07-01)

Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disability
由: Janelle Elizabeth O'Brien, et al.
出版: (2013-10-01)

Molecular determinants of μ-conotoxin KIIIA interaction with the human voltage-gated sodium channel NaV1.7
由: Ian H. Kimball, et al.
出版: (2023-03-01)

Abstract P-10: Comparison of Ion Coordination in Similar Selectivity Filters of Bacterial Sodium and Eukaryotic Calcium Voltage-Gated Channels
由: Ivan N. Terterov, et al.
出版: (2019-06-01)

Vaccinations and Dravet Syndrome
由: Christian M. Korff
出版: (2015-12-01)

Animal Toxins Can Alter the Function of Nav1.8 and Nav1.9
由: John Gilchrist, et al.
出版: (2012-08-01)

SCN1B Genetic Variants: A Review of the Spectrum of Clinical Phenotypes and a Report of Early Myoclonic Encephalopathy
由: Zahra Zhu, et al.
出版: (2022-10-01)

Tetrodotoxin, a Candidate Drug for Nav1.1-Induced Mechanical Pain?
由: César Mattei
出版: (2018-02-01)