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.

June 4, 2020

Thalamic and cortical hyperexcitability in juvenile myoclonic epilepsy

Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
Giovanni AssenzaVincenzo Di Lazzaro
June 12, 2020
Open Access

Genetic generalized epilepsies with frontal lesions mimicking migratory disorders on the epilepsy monitoring unit

Epilepsia Open
Susanne FauserChristian G Bien
July 6, 2020
Case Report

Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
L A KalashnikovaM V Kostyreva
August 13, 2020

How to diagnose and classify idiopathic (genetic) generalized epilepsies

Epileptic Disorders : International Epilepsy Journal with Videotape
Ayse Deniz ElmaliMichalis Koutroumanidis
July 24, 2020

Do interictal EEG findings reflect cognitive function in juvenile myoclonic epilepsy?

Epilepsy & Behavior : E&B
Zeynep Ezgi BalcikDilek Atakli
August 6, 2020
Open Access

A Case of Myoclonic Epilepsy Presenting with Status Epilepticus in an Elderly Male Patient

Journal of Neurosciences in Rural Practice
Halil Onder
July 10, 2020

Cloning and characterization of Litopenaeus vannamei cystainB-like in WSSV infection

Fish & Shellfish Immunology
Rui-Feng Zou, Qing-Hui Liu
August 11, 2020
Case Report
Open Access

Paraneoplastic Cerebellar Degeneration Secondary to BRAF Mutant Melanoma Metastasis from an Occult Primary Cancer

Case Reports in Oncology
Omar Jiménez-ZarazúaJaime Daniel Mondragón
August 9, 2020

Can we predict drug response by functional connectivity in patients with juvenile myoclonic epilepsy?

Clinical Neurology and Neurosurgery
Jiyoung KimKang Min Park
July 10, 2020
Case Report
Open Access

Long term follow up after transorbital penetrating injury: A case report

American Journal of Ophthalmology Case Reports
Caroline VlokaSusan Stefko
June 20, 2020
Case Report
Open Access

Variant ataxia-telangiectasia in a child presenting with laryngeal dystonia

The Turkish Journal of Pediatrics
Pınar ArıcanPınar Gençpınar
June 26, 2020
Open Access

Motor hyperactivation during cognitive tasks: An endophenotype of juvenile myoclonic epilepsy

Epilepsia
Lorenzo CaciagliMatthias J Koepp
June 26, 2020

Immunogenetic protective factors in Genetic Generalized Epilepsy

Epilepsy Research
João ChavesBárbara Leal

Sign up to follow this feed and discover related papers.

Related Feeds

ALS

Amyotrophic Lateral Sclerosis (ALS), also known as motor neuron disease, is associated with the death of neurons that control voluntary muscles. Discover the latest research on ALS here.

ALS & FTD: TDP-43

ALS shares with a considerable proportion of FTD cases the same neuropathological substrate, namely, inclusions of abnormally phosphorylated protein tdp-43 (ptdp-43). Here are the latest discoveries pertaining to ptdp-43 and these diseases.

ALS - Pathogenic Mechanisms

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. Here is the latest research investigating pathogenic mechanisms that underlie this genetically heterogeneous disorder.

ALS - Phenotypes

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. Here is the latest research investigating phenotypes associated with this genetically heterogeneous disorder.

ALS: Genetics

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. ALS is a genetically heterogeneous disorder with several causative genes. Here are the latest discoveries pertaining to the genetics of this disease.

ALS: Prions

Prions are misfolded proteins which characterize several fatal neurodegenerative diseases. Prion-like mechanisms are associated with the pathogenesis of Amyotrophic Lateral Sclerosis (ALS). Here are the latest discoveries pertaining to this disease.

ALS: Stress Granules

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease characterized by cytoplasmic protein aggregates within motor neurons. TDP-43 is an ALS-linked protein that is known to regulate splicing and storage of specific mRNAs into stress granules, which have been implicated in formation of ALS protein aggregates. Here is the latest research.

ALS: Therapies

Amyotrophic Lateral Sclerosis (ALS), also known as motor neuron disease, is associated with the death of neurons that control voluntary muscles. Discover the latest research on ALS therapies here.

ALS: Transposon de-silencing

Transposon silencing is a form of transcriptional gene silencing. These gene silencing mechanisms are impaired in Amyotrophic lateral sclerosis (ALS). Here are the latest discoveries pertaining to transposon silencing and this disease.

Age-related Dementia

Age-related dementia (Alzheimer's disease) results from the destructive impact of the pulse on cerebral vasculature. Evidence is reviewed that the neuropathology of the dementia is caused by the breakdown of small cerebral vessels (silent microbleeds), that the microbleeds result from pulse-induced damage to the cerebral vessels, and that pulse becomes increasingly destructive with age, because of the age-related stiffening of the aorta and great arteries, which causes an increase in the intensity of the pressure pulse. Discover the latest research on age-related dementia here.

© 2020 Meta ULC. All rights reserved
/feed-previews/unverricht-lundborg-syndrome/13376d71-54a9-4579-a3eb-a2350681e66a