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).

Sonraí bibleagrafaíochta
Príomhchruthaitheoirí:	Laura Black, Deborah Gaebler-Spira
Formáid:	Alt
Teanga:	English
Foilsithe / Cruthaithe:	Pediatric Neurology Briefs Publishers 2016-11-01
Sraith:	Pediatric Neurology Briefs
Ábhair:	dravet syndrome neurologic gait disorders nav1.1 voltage gated sodium channel
Rochtain ar líne:	https://www.pediatricneurologybriefs.com/articles/3790

Míreanna comhchosúla

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

Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome
de réir: Moran Rubinstein, et al.
Foilsithe / Cruthaithe: (2015-01-01)

Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome
de réir: Joanna Mattis, et al.
Foilsithe / Cruthaithe: (2022-02-01)

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

Phenotypes of Dravet Syndrome
de réir: Rebecca Garcia-Sosa, et al.
Foilsithe / Cruthaithe: (2016-08-01)

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

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

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

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

Focal Scn1a knockdown induces cognitive impairment without seizures
de réir: Alex C. Bender, et al.
Foilsithe / Cruthaithe: (2013-06-01)

NaV1.1 is essential for proprioceptive signaling and motor behaviors
de réir: Cyrrus M Espino, et al.
Foilsithe / Cruthaithe: (2022-10-01)

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

Compromised function in the Nav1.2 Dravet syndrome mutation R1312T
de réir: Christoph Lossin, et al.
Foilsithe / Cruthaithe: (2012-09-01)

Cell-Adhesion Properties of β-Subunits in the Regulation of Cardiomyocyte Sodium Channels
de réir: Samantha C. Salvage, et al.
Foilsithe / Cruthaithe: (2020-07-01)

Dravet Variant SCN1AA1783V Impairs Interneuron Firing Predominantly by Altered Channel Activation
de réir: Nikolas Layer, et al.
Foilsithe / Cruthaithe: (2021-10-01)

Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet syndrome
de réir: Kevin M Goff, et al.
Foilsithe / Cruthaithe: (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
de réir: Li Chunli, et al.
Foilsithe / Cruthaithe: (2016-12-01)

Recent developments regarding voltage-gated sodium channel blockers for the treatment of inherited and acquired neuropathic pain syndromes
de réir: Jonathan W. Theile, et al.
Foilsithe / Cruthaithe: (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
de réir: Valery Zayat, et al.
Foilsithe / Cruthaithe: (2023-01-01)

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

Genetic Variants in the SCN9A Gene are Detected in a Minority of Erythromelalgia Patients
de réir: Mari Skystad Kvernebo, et al.
Foilsithe / Cruthaithe: (2025-01-01)

Insights into the voltage-gated sodium channel, NaV1.8, and its role in visceral pain perception
de réir: J. Westley Heinle, et al.
Foilsithe / Cruthaithe: (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
de réir: Jennifer R. Deuis, et al.
Foilsithe / Cruthaithe: (2022-01-01)

Role of the hippocampus in Nav1.6 (Scn8a) mediated seizure resistance
de réir: Christopher D. Makinson, et al.
Foilsithe / Cruthaithe: (2014-08-01)

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

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

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

Patient with Dravet syndrome: A case report
de réir: Rukesh Yadav, et al.
Foilsithe / Cruthaithe: (2022-05-01)

Fenestropathy of Voltage-Gated Sodium Channels
de réir: Tamer M. Gamal El-Din, et al.
Foilsithe / Cruthaithe: (2022-02-01)

Conotoxins Targeting Neuronal Voltage-Gated Sodium Channel Subtypes: Potential Analgesics?
de réir: Jeffrey R. McArthur, et al.
Foilsithe / Cruthaithe: (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
de réir: Sarah Thull, et al.
Foilsithe / Cruthaithe: (2020-08-01)

Deficiency of autism-related Scn2a gene in mice disrupts sleep patterns and circadian rhythms
de réir: Zhixiong Ma, et al.
Foilsithe / Cruthaithe: (2022-06-01)

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

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

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

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

Vaccinations and Dravet Syndrome
de réir: Christian M. Korff
Foilsithe / Cruthaithe: (2015-12-01)

Animal Toxins Can Alter the Function of Nav1.8 and Nav1.9
de réir: John Gilchrist, et al.
Foilsithe / Cruthaithe: (2012-08-01)

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

Tetrodotoxin, a Candidate Drug for Nav1.1-Induced Mechanical Pain?
de réir: César Mattei
Foilsithe / Cruthaithe: (2018-02-01)