Wioletta Krysa - Concepedia

Author

Wioletta Krysa

Institute of Psychiatry and Neurology

Also Known As

Berry Kremer, Katarzyna Jachinska, Rafal Rola, W Krysa, W. Krysa, Wioletta Krysa

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Institute of Psychiatry and Neurology Medical University of Silesia Polish Academy of Sciences

About

Wioletta Krysa is an author at Institute of Psychiatry and Neurology specializing in medicine, pathology, and neuromuscular pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	124
2	Education	1	1	20
3	Health Sciences	1	1	23
4	Biology	1	1	29
5	Biostatistics	1	1	20

Wioletta Krysa

Publications

315

Citations

H-Index

Page 1

	Year	Citations
Self-awareness of Motor Dysfunction in Patients with Huntington's Disease in Comparison to Parkinson's Disease and Cervical Dystonia Emilia J. Sitek, Witold Sołtan, Dariusz Wieczorek, Journal of the International Neuropsychological Society	2011	71
Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes Ewelina Elert‐Dobkowska, Iwona Stępniak, Wioletta Krysa, Neurogenetics	2019	50
Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients Ewelina Elert‐Dobkowska, Iwona Stępniak, Wioletta Krysa, Journal of the Neurological Sciences Rare DiseasesReep1 Gene MutationsPolish PatientsGenetic DisorderMedicine	2015	32
Screening for the hereditary spastic paraplaegias SPG4 and SPG3A with the multiplex ligation-dependent probe amplification technique in a large population of affected individuals Ewelina Elert‐Dobkowska, Marta Rajkiewicz, Elżbieta Zdzienicka, Neurological Sciences BiologyGenetic DisorderMedicineGeneticsPathology	2011	29
The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients Anna Sułek, Elżbieta Zdzienicka, Maria Rakowicz, Neurologia i Neurochirurgia Polska	2010	24
Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients. Aleksandra Nadaj‐Pakleza, Anna Sułek, Wioletta Krysa, PubMed Genetic TestingMuscle FunctionPathologyEighteen PatientsOrthopaedic Surgery	2011	23
The personal experience of parenting a child with Juvenile Huntington’s Disease: perceptions across Europe Virginia Eatough, Helen Santini, Christine Eiser, European Journal of Human Genetics Family MedicineChild PsychologyChild Well-beingFamily InvolvementChild Mental Health	2013	20
High relative frequency of SCA1 in Poland reflecting a potential founder effect Wioletta Krysa, Maria Rakowicz, Walentyna Szirkowiec, Neurological Sciences Allelic VariantMendelian DisorderGenetic DisorderGeneticsSpinocerebellar Ataxias	2016	20
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. Anna Sułek, Wioletta Krysa, Elżbieta Zdzienicka, PubMed	2008	13
Rapid detection of large expansions in progressive myoclonus epilepsy type 1, myotonic dystrophy type 2 and spinocerebellar ataxia type 8 Wioletta Krysa, Marta Rajkiewicz, Anna Sutek Neurologia i Neurochirurgia Polska	2012	12

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