Christine Zuhlke
Ratzeburger Allee 160
Luebeck, SH 23538, Germany
Luebeck, SH 23538, Germany
Last Updated: 09/26/2026
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Found 14 publications
Repeat length in spinocerebellar ataxia type 4 (SCA4) predicts age at onset and disease severity.
Journal: Journal of neurology
Published: June 05, 2024
Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year Study.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 24, 2022
A case of Huntington's disease with two reduced penetrance alleles.
Journal: Clinical neurology and neurosurgery
Published: December 21, 2020
Clinical spectrum of the pentanucleotide repeat expansion in the RFC1 gene in ataxia syndromes.
Journal: Neurology
Published: January 13, 2020
Spinocerebellar ataxia 28: a novel AFG3L2 mutation in a German family with young onset, slow progression and saccadic slowing.
Journal: Cerebellum & ataxias
Published: December 02, 2015
Psychosis Complicating Friedreich Ataxia.
Journal: Movement disorders clinical practice
Published: August 10, 2014
Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14.
Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14.
Journal: Cerebellum (London, England)
Published: September 14, 2013
A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.
Journal: European journal of medical genetics
Published: September 09, 2013
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.
Journal: Journal of neurology
Published: July 18, 2013
Last Updated: 09/26/2026