W. Krysa

发表

Peripheral nerve involvement in myotonic dystrophy type 2 - similar or different than in myotonic dystrophy type 1?

M. Gaweł, A. Kaminska, A. Łusakowska, 2015, Neurologia i neurochirurgia polska.

Familial 15q11.2 Micro deletions are not Fully Penetrant in Two Cases with Hereditary Spastic Paraplegia and Dysmorphic Features

D. Hoffman-Zacharska, J. Zaremba, A. Sulek, 2014 .

The personal experience of parenting a child with Juvenile Huntington’s Disease: perceptions across Europe

Jonathan A. Smith, B. Landwehrmeyer, V. Eatough, 2013, European Journal of Human Genetics.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes

J. Pilch, J. Zaremba, A. Sobańska, 2019, neurogenetics.

Value of short exercise and short exercise with cooling tests in the diagnosis of myotonic dystrophies (DM1 AND DM2)

M. Gaweł, A. Kaminska, E. Szmidt-Sałkowska, 2014, Muscle & nerve.

Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients

J. Pilch, C. Beetz, M. Rudzińska, 2015, Journal of the Neurological Sciences.

Hereditary form of prion disease in Poland.

J. Zimowski, W. Lojkowska, J. Zaremba, 2012, Neurologia i neurochirurgia polska.

Does quantitative EMG differ myotonic dystrophy type 2 and type 1?

M. Gaweł, A. Kaminska, E. Szmidt-Sałkowska, 2014, Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology.

Rapid detection of large expansions in progressive myoclonus epilepsy type 1, myotonic dystrophy type 2 and spinocerebellar ataxia type 8.

W. Krysa, M. Rajkiewicz, A. Sułek, 2012, Neurologia i neurochirurgia polska.

Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes

J. Pilch, J. Zaremba, A. Sobańska, 2019, neurogenetics.

Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.

A. Kaminska, A. Nadaj-Pakleza, H. Kwiecinski, 2011, Folia morphologica.

High relative frequency of SCA1 in Poland reflecting a potential founder effect

J. Zaremba, W. Krysa, W. Szirkowiec, 2016, Neurological Sciences.

Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.

D. Hoffman-Zacharska, J. Zaremba, W. Krysa, 2008, Neurologia i neurochirurgia polska.

Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.

A. Kaminska, H. Kwiecinski, J. Zaremba, 2018, Neurologia i neurochirurgia polska.

WITHDRAWN: Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.

A. Kaminska, H. Kwiecinski, J. Zaremba, 2018, Neurologia i neurochirurgia polska.

Screening for the hereditary spastic paraplaegias SPG4 and SPG3A with the multiplex ligation-dependent probe amplification technique in a large population of affected individuals

J. Zaremba, W. Krysa, M. Rajkiewicz, 2013, Neurological Sciences.

Self-awareness of Motor Dysfunction in Patients with Huntington's Disease in Comparison to Parkinson's Disease and Cervical Dystonia

R. Reilmann, M. Harciarek, E. Sitek, 2011, Journal of the International Neuropsychological Society.

A molecular and cytogenetic investigation of FMR1 gene premutations in Polish patients with primary ovarian insufficiency.

S. Radowicki, J. Zaremba, W. Krysa, 2011, European journal of obstetrics, gynecology, and reproductive biology.

The needle EMG findings in myotonia congenita.

M. Gaweł, A. Kaminska, M. Nojszewska, 2019, Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology.

Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia.

J. Zaremba, W. Krysa, M. Rajkiewicz, 2008, Neurologia i neurochirurgia polska.

Recommendations for the Predictive Genetic Test in Huntington's Disease Committee and Working Group 'genetic Testing Counselling' of the European Huntington Disease Network †, ‡

D. Craufurd, R. Macleod, F. Squitieri, 2022 .

Huntington ’ s Disease and Sleep Related Breathing Disorders

J. Antczak, G. Witkowski, R. Rola, 2015 .