Marta Rajkiewicz
Warsaw, MZ, Poland
Last Updated: 09/26/2026
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Found 9 publications
Frequently observed polyneuropathy expands phenotypic spectrum of apparently pure autosomal dominant hereditary spastic paraplegias.
Journal: Neurologia i neurochirurgia polska
Published: June 25, 2024
WITHDRAWN: Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.
Journal: Neurologia i neurochirurgia polska
Published: March 27, 2018
Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.
Journal: Neurologia i neurochirurgia polska
Published: October 03, 2017
Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.
Journal: Journal of the neurological sciences
Published: July 24, 2015
Peripheral nerve involvement in myotonic dystrophy type 2 - similar or different than in myotonic dystrophy type 1?
Journal: Neurologia i neurochirurgia polska
Published: December 08, 2014
Does quantitative EMG differ myotonic dystrophy type 2 and type 1?
Journal: Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology
Published: December 01, 2013
Rapid detection of large expansions in progressive myoclonus epilepsy type 1, myotonic dystrophy type 2 and spinocerebellar ataxia type 8.
Journal: Neurologia i neurochirurgia polska
Published: May 15, 2012
Familial occurrence of FXTAS caused by premutation in the FMR1 gene
Journal: Neurologia i neurochirurgia polska
Published: November 22, 2011
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Last Updated: 09/26/2026