Gerstmann-Straussler-Scheinker Disease

Gerstmann-Straussler-Scheinker disease is a rare neurodegenerative disorder caused by prions and characterized by symptoms similar to other prion-associated diseases. Here is the latest research.

December 29, 2021
Review
Open Access

Differential Accumulation of Misfolded Prion Strains in Natural Hosts of Prion Diseases.

Viruses
Zoe J LambertM Heather West Greenlee
June 21, 2021

[Prion diseases or transmissible spongiform encephalopathies].

La Revue de médecine interne
J-P Brandel
December 17, 2020
Open Access

Structural Features of Heparin and Its Interactions With Cellular Prion Protein Measured by Surface Plasmon Resonance.

Frontiers in Molecular Biosciences
So Young KimRobert J Linhardt
January 1, 2020
Case Report
Open Access

A case of Gerstmann-Straussler-Scheinker (GSS) disease with supranuclear gaze palsy

Journal of Clinical Movement Disorders
Nicole A UfkesMarian L Dale
September 19, 2019

Prion Disease

Seminars in Neurology
Kelly J Baldwin, Cynthia M Correll
July 25, 2018
Open Access

Human prion diseases: current issues

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
N N ZavadenkoE N Saverskaya
January 20, 2018

In Situ Tissue Labeling of Cerebral Amyloid Using HIV-Related Tat Peptide

Molecular Neurobiology
E MadernaG Giaccone
November 18, 2017
Case Report

Gerstmann-Straussler-Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy

European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies
L MumoliA Gambardella
September 2, 2017
Open Access

Purification and Fibrillation of Full-Length Recombinant PrP

Methods in Molecular Biology
Natallia MakaravaIlia V Baskakov
April 19, 2017
Open Access

A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Straussler-Scheinker syndrome with P102L mutation in PRNP gene

Neurosciences : the Official Journal of the Pan Arab Union of Neurological Sciences
Ling LongZhengqi Lu
January 23, 2017
Review

Neuroradiology of human prion diseases, diagnosis and differential diagnosis

La Radiologia medica
Simona GaudinoCesare Colosimo
November 5, 2016
Review

Oxidative stress and mitochondrial dysfunction-linked neurodegenerative disorders

Neurological Research
Md Torequl Islam
May 20, 2016
Review
Open Access

Prions in dentistry: A need to be concerned and known

Journal of Oral and Maxillofacial Pathology : JOMFP
B SushmaShambhvi A Malik
July 16, 2015
Open Access

Prion Protein Prolines 102 and 105 and the Surrounding Lysine Cluster Impede Amyloid Formation.

The Journal of Biological Chemistry
Allison KrausByron Caughey

Sign up to follow this feed and discover related papers.

Related Feeds

3D Cellular Models of Brain and Neurodegeneration

Brain organoids are three-dimensional in vitro cellular models of the brain that can recapitulate many processes such as the neurodevelopment. In addition, these organoids can be combined with other cell types, such as neurons and astrocytes to study their interactions in assembloids. Disease processes can also be modeled by induced pluripotent stem cell-derived organoids and assembloids from patients with neurodegenerative disorders. Discover the latest research on the models here.

ALS & FTD: TDP-43

TAR DNA-binding protein 43 (TDP-43) is a pathological protein identified in sporadic Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD). Here are the latest discoveries pertaining to TDP-43 and these diseases.

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: Pathogenic Mechanisms

Amyotrophic Lateral Sclerosis 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 neurodegenerative disorder characterized phenotypically by progressive muscle weakness. Clinical phenotypes of ALS can be classified based on the pattern, level, and area of onset (e.g. bulbar, cervical, lumbar). Here is the latest research investigating phenotypes of ALS.

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 is the latest research on ALS and prions.

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 in this field.

ALS: Therapies

Amyotrophic Lateral Sclerosis (ALS) is associated with the death of neurons that control voluntary muscles. This feed followes the latest research into therapies for this progressive neurodegenerative disease.

Age-related Dementia

Dementias are a group of conditions, including Alzheimer's disease, vascular dementia, and frontotemporal dementia, characterized by deficiencies in cognitive abilities. Age-related dementia refers to dementias that occur in older individuals, usually 60+ years old, in contrast to early-onset dementia. Follow the latest research on age-related dementia here.

Alexander Disease

Alexander disease is a rare leukodystrophy caused by mutations in the astrocyte-specific intermediate filament protein glial fibrillary acidic protein (GFAP). Here is the latest research on this disease.

© 2022 Meta ULC. All rights reserved
/feed-previews/gerstmann-straussler-scheinker/a3c4889b-b190-4e1a-8447-fdfae7aa76dd