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
Review
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

Sign up to follow this feed and discover related papers.

Trending Feeds

COVID-19

Coronaviruses encompass a large family of viruses that cause the common cold as well as more serious diseases, such as the ongoing outbreak of coronavirus disease 2019 (COVID-19; formally known as 2019-nCoV). Coronaviruses can spread from animals to humans; symptoms include fever, cough, shortness of breath, and breathing difficulties; in more severe cases, infection can lead to death. This feed covers recent research on COVID-19.

Synthetic Genetic Array Analysis

Synthetic genetic arrays allow the systematic examination of genetic interactions. Here is the latest research focusing on synthetic genetic arrays and their analyses.

Congenital Hyperinsulinism

Congenital hyperinsulinism is caused by genetic mutations resulting in excess insulin secretion from beta cells of the pancreas. Here is the latest research.

Neural Activity: Imaging

Imaging of neural activity in vivo has developed rapidly recently with the advancement of fluorescence microscopy, including new applications using miniaturized microscopes (miniscopes). This feed follows the progress in this growing field.

Chronic Fatigue Syndrome

Chronic fatigue syndrome is a disease characterized by unexplained disabling fatigue; the pathology of which is incompletely understood. Discover the latest research on chronic fatigue syndrome here.

Epigenetic Memory

Epigenetic memory refers to the heritable genetic changes that are not explained by the DNA sequence. Find the latest research on epigenetic memory here.

Cell Atlas of the Human Eye

Constructing a cell atlas of the human eye will require transcriptomic and histologic analysis over the lifespan. This understanding will aid in the study of development and disease. Find the latest research pertaining to the Cell Atlas of the Human Eye here.

Femoral Neoplasms

Femoral Neoplasms are bone tumors that arise in the femur. Discover the latest research on femoral neoplasms here.

STING Receptor Agonists

Stimulator of IFN genes (STING) are a group of transmembrane proteins that are involved in the induction of type I interferon that is important in the innate immune response. The stimulation of STING has been an active area of research in the treatment of cancer and infectious diseases. Here is the latest research on STING receptor agonists.

© 2021 Meta ULC. All rights reserved
/feed-previews/unverricht-lundborg-syndrome/13376d71-54a9-4579-a3eb-a2350681e66a