Marion Wandzel

Nancy, France

Last Updated: 09/26/2026

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Found 16 publications

Cerebellar cognitive affective syndrome (CCAS) and [18F]-FDG PET findings in spinocerebellar ataxia type SCA27B.

Cerebellar cognitive affective syndrome (CCAS) and [18F]-FDG PET findings in spinocerebellar ataxia type SCA27B.

Journal: Journal of neurology

Published: March 07, 2026

Hyperhomocysteinemia and Vitamin B Deficiency as Potential Aggravating Factors in Huntington's Disease: A Prospective Monocentric Study.

Hyperhomocysteinemia and Vitamin B Deficiency as Potential Aggravating Factors in Huntington's Disease: A Prospective Monocentric Study.

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

Published: February 20, 2026

Late-onset cerebellar ataxia in three European patients with repeat expansions in RFC1 and FGF14: a case series.

Late-onset cerebellar ataxia in three European patients with repeat expansions in RFC1 and FGF14: a case series.

Journal: Journal of neurology

Published: April 21, 2025

Oculomotor Findings in Spinocerebellar Ataxia 27B: A Case Series.

Oculomotor Findings in Spinocerebellar Ataxia 27B: A Case Series.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: December 09, 2024

Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophy.

Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophy.

Journal: Brain : a journal of neurology

Published: November 20, 2024

How to distinguish spinocerebellar ataxia 27B from late onset cerebellar ataxia: insights from a case-control study.

How to distinguish spinocerebellar ataxia 27B from late onset cerebellar ataxia: insights from a case-control study.

Journal: Journal of neurology

Published: October 09, 2024

Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients.

Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients.

Journal: Journal of medical genetics

Published: April 02, 2024

Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur-Chung neurodevelopmental syndrome.

Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur-Chung neurodevelopmental syndrome.

Journal: American journal of medical genetics. Part A

Published: March 05, 2024

Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions.

Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions.

Journal: EBioMedicine

Published: October 02, 2023

A common flanking variant is associated with enhanced meiotic stability of the FGF14 -SCA27B locus.

A common flanking variant is associated with enhanced meiotic stability of the FGF14 -SCA27B locus.

Journal: bioRxiv : the preprint server for biology

Published: July 10, 2023

Non-GAA Repeat Expansions in FGF14 Are Likely Not Pathogenic-Reply to: "Shaking Up Ataxia: FGF14 and RFC1 Repeat Expansions in Affected and Unaffected Members of a Chilean Family".

Non-GAA Repeat Expansions in FGF14 Are Likely Not Pathogenic-Reply to: "Shaking Up Ataxia: FGF14 and RFC1 Repeat Expansions in Affected and Unaffected Members of a Chilean Family".

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

Published: June 05, 2023

A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus.

A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus.

Journal: Nature genetics

Published: May 11, 2023

Showing 1-12 of 16

Last Updated: 09/26/2026