Corien C. Bemelmans-Verschuuren

Groningen, GR, Netherlands

Last Updated: 09/26/2026

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Found 38 publications

Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch Cohort.

Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch Cohort.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 23, 2025

Corrigendum to "Genetics of upper limb tremor in clinical practice: a systematic literature review" [Parkinsonism and Related disorders volume "in press" (2025) PRD 107981].

Corrigendum to "Genetics of upper limb tremor in clinical practice: a systematic literature review" [Parkinsonism and Related disorders volume "in press" (2025) PRD 107981].

Journal: Parkinsonism & related disorders

Published: September 27, 2025

Genetics of upper limb tremor in clinical practice: a systematic literature review.

Genetics of upper limb tremor in clinical practice: a systematic literature review.

Journal: Parkinsonism & related disorders

Published: April 29, 2025

Prevalence of Pathogenic Variants and Eligibility Criteria for Genetic Testing in Patients Who Visit a Memory Clinic.

Prevalence of Pathogenic Variants and Eligibility Criteria for Genetic Testing in Patients Who Visit a Memory Clinic.

Journal: Neurology

Published: January 27, 2025

High Prevalence of the Intronic GAA-FGF14 Repeat Expansion in Dutch Patients With Late-Onset Ataxia.

High Prevalence of the Intronic GAA-FGF14 Repeat Expansion in Dutch Patients With Late-Onset Ataxia.

Journal: Neurology. Genetics

Published: September 30, 2024

Identification and Copy Number Variant Analysis of Enhancer Regions of Genes Causing Spinocerebellar Ataxia.

Identification and Copy Number Variant Analysis of Enhancer Regions of Genes Causing Spinocerebellar Ataxia.

Journal: International journal of molecular sciences

Published: September 07, 2024

A Likely Pathogenic variant in the KBTBD13 Gene: A Case Series of Three Patients with Nemaline Myopathy Type 6.

A Likely Pathogenic variant in the KBTBD13 Gene: A Case Series of Three Patients with Nemaline Myopathy Type 6.

Journal: Journal of neuromuscular diseases

Published: September 06, 2024

A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder.

A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: April 19, 2024

A cross-sectional study in 18 patients with typical and mild forms of nemaline myopathy in the Netherlands.

A cross-sectional study in 18 patients with typical and mild forms of nemaline myopathy in the Netherlands.

Journal: Neuromuscular disorders : NMD

Published: March 06, 2024

The natural history of progressive myoclonus ataxia.

The natural history of progressive myoclonus ataxia.

Journal: Neurobiology of disease

Published: March 02, 2024

Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients With Cerebellar Ataxia.

Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients With Cerebellar Ataxia.

Journal: Neurology. Genetics

Published: June 06, 2022

Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxia.

Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxia.

Journal: Journal of neurology

Published: May 05, 2022

Showing 1-12 of 38

Last Updated: 09/26/2026