Unverricht-Lundborg Syndrome

Unverricht-Lundborg Syndrome is a type of progressive myoclonus epilepsy characterized by involuntary muscle jerking/twitching, seizures, muscle rigidity, and convulsions. Discover the latest research on this rare inherited form of epilepsy here.

December 29, 2020
Open Access

Ataxia Prevalence in Primary Orthostatic Tremor

Tremor and Other Hyperkinetic Movements
Rebecca ThompsonDiego Torres-Russotto
November 23, 2020
Open Access

Multivariate white matter alterations are associated with epilepsy duration

The European Journal of Neuroscience
Thomas W OwenPeter N Taylor
December 30, 2020

Lafora body disease: a case of progressive myoclonic epilepsy

BMJ Case Reports
Ranjot KaurSudarshan Kumar Sharma
November 17, 2020
Open Access

TRPM7 as a Candidate Gene for Vestibular Migraine

Frontiers in Neurology
Eun Hye OhJae-Hwan Choi
December 6, 2020

Urinary clusterin and cystatin B as biomarkers of tubular injury in dogs following envenomation by the European adder

Research in Veterinary Science
E GordinT Spillmann
December 4, 2020
Open Access

Cross Talk at the Cytoskeleton-Plasma Membrane Interface: Impact on Neuronal Morphology and Functions

International Journal of Molecular Sciences
Rossella Di GiaimoMarianna Crispino
December 22, 2020
Case Report
Open Access

Case Report: Four Cases of Panayiotopoulos Syndrome Evolving to Juvenile Myoclonic Epilepsy

Frontiers in Neurology
Hideo EnokiAyataka Fujimoto
December 18, 2020

Blepharoptosis and dysarthria in a boy aged 2 years

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Li-Rong ZhaoGuang-Lu Yang
December 3, 2020
Open Access

Trait impulsivity in Juvenile Myoclonic Epilepsy.

Annals of Clinical and Translational Neurology
Amy ShakeshaftBIOJUME Consortium
December 18, 2020
Case Report
Open Access

CSF HIV RNA Escape in Opsoclonus-Myoclonus-Ataxia Syndrome: Case Report and Review of the Literature

Frontiers in Neurology
Cabaraux PierreManto Mario
December 22, 2020
Case Report
Open Access

Case Report: Distinctive EEG Patterns in SCARB-2 Related Progressive Myoclonus Epilepsy

Frontiers in Genetics
Mostafa HotaitAhmad Beydoun
January 1, 2021

Surround inhibition in patients with juvenile myoclonic epilepsy

Neurological Research
Bengi Gul TurkMeral Kiziltan
December 12, 2020

Rare case of Marchiafava-Bignami disease due to thiamine deficiency and malnutrition

BMJ Case Reports
Stephanie KinsleyDavid Shulman
December 18, 2020
Open Access

Epilepsy protein Efhc1/myoclonin1 is expressed in cells with motile cilia but not in neurons or mitotic apparatuses in brain

Scientific Reports
Toshimitsu SuzukiKazuhiro Yamakawa
November 26, 2020
Case Report

Novel ACOX1 mutations in two siblings with peroxisomal acyl-CoA oxidase deficiency

Brain & Development
Atsushi MoritaHidetoshi Takada
December 15, 2020
Open Access

Systematic review of CMTX1 patients with episodic neurological dysfunction.

Annals of Clinical and Translational Neurology
Dandan TianXu Liu
January 19, 2021

Leucine Carboxyl Methyltransferase 1 Overexpression Protects Against Cognitive and Electrophysiological Impairments in Tg2576 APP Transgenic Mice

Journal of Alzheimer's Disease : JAD
Madhumathi GnanaprakashRussell E Nicholls
November 30, 2020

Household poverty, schooling, stigma and quality of life in adolescents with epilepsy in rural Uganda

Epilepsy & Behavior : E&B
Ronald AnguzuRichard Idro
November 14, 2020

Revisiting the clinical impact of variants in EFHC1 in patients with different phenotypes of genetic generalized epilepsy

Epilepsy & Behavior : E&B
Marina C GonsalesIscia Lopes-Cendes

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