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Last Updated: 03/06/2025

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Found 452 publications

Gerstmann-Straussler-Scheinker disease: Lessons from two new Indian kindreds.

Gerstmann-Straussler-Scheinker disease: Lessons from two new Indian kindreds.

Journal: Parkinsonism & related disorders
Published: November 09, 2024

Involvement of the nigrostriatal system in Gerstman-Sträussler-Scheinker disease with the PRNP-P102L mutation.

Involvement of the nigrostriatal system in Gerstman-Sträussler-Scheinker disease with the PRNP-P102L mutation.

Journal: Journal of the neurological sciences
Published: May 16, 2024

Novel method for classification of prion diseases by detecting PrPres signal patterns from formalin-fixed paraffin-embedded samples.

Novel method for classification of prion diseases by detecting PrPres signal patterns from formalin-fixed paraffin-embedded samples.

Journal: Prion
Published: April 16, 2024

Clinical characteristics and diagnostics of human spongiform encephalopathies: an update

Clinical characteristics and diagnostics of human spongiform encephalopathies: an update

Journal: Der Nervenarzt
Published: February 28, 2024

Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Sträussler-Scheinker disease.

Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Sträussler-Scheinker disease.

Journal: Neurobiology of disease
Published: January 26, 2024

F198S Gerstmann-Sträussler-Scheinker Syndrome With Parkinsonism, Dyskinesia, and Abnormal (I-123)-FP-CIT Single-Photon Emission Computed Tomography: A Case Report.

F198S Gerstmann-Sträussler-Scheinker Syndrome With Parkinsonism, Dyskinesia, and Abnormal (I-123)-FP-CIT Single-Photon Emission Computed Tomography: A Case Report.

Journal: Cureus
Published: October 09, 2023

Serial changes in regional cerebral blood flow in Gerstmann-Sträussler-Scheinker disease caused by a Pro-to-Leu mutation at codon 105 in the prion protein gene.

Serial changes in regional cerebral blood flow in Gerstmann-Sträussler-Scheinker disease caused by a Pro-to-Leu mutation at codon 105 in the prion protein gene.

Journal: Prion
Published: September 14, 2023

Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology.

Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology.

Journal: Movement disorders clinical practice
Published: June 07, 2023

NGS study in a sicilian case series with a genetic diagnosis for Gerstmann-Sträussler-Scheinker syndrome (PRNP, p.P102L).

NGS study in a sicilian case series with a genetic diagnosis for Gerstmann-Sträussler-Scheinker syndrome (PRNP, p.P102L).

Journal: Molecular biology reports
Published: May 16, 2023

Gerstmann-Sträussler disease: a familial case with common PRNP mutation and atypical features

Gerstmann-Sträussler disease: a familial case with common PRNP mutation and atypical features

Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: February 27, 2023

A family with mental disorder as the first symptom finally confirmed with Gerstmann-Sträussler-Scheinker disease with P102L mutation in PRNP gene - case report.

A family with mental disorder as the first symptom finally confirmed with Gerstmann-Sträussler-Scheinker disease with P102L mutation in PRNP gene - case report.

Journal: Prion
Published: February 27, 2023

Sleep in Gerstmann-Straüssler-Scheinker disease.

Sleep in Gerstmann-Straüssler-Scheinker disease.

Journal: Sleep medicine
Published: February 26, 2023
Showing 1-12 of 452

Last Updated: 03/06/2025