Iwona Stępniak - Concepedia

Author

Iwona Stępniak

Institute of Psychiatry and Neurology ORCID

Also Known As

Halina Sienkiewicz-Jarosz, I. Stepniak, I. Stępniak, Iwona Stepniak, Iwona Stępniak, Jacek Zaremba

Publications

777

Citations

H-Index

Concepts

All Affiliations

Institute of Psychiatry and Neurology Institute of Physiology and Pathology of Hearing Polish Academy of Sciences Medical University of Warsaw Medical University of Silesia

About

Iwona Stępniak is an author at Institute of Psychiatry and Neurology specializing in medicine, molecular genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	165
2	Molecular Genetics	2	2	61
3	Pathology	2	2	61
4	Biology	1	1	29
5	Neurology	1	1	104

Iwona Stępniak

Publications

307

Citations

H-Index

Page 1

	Year	Citations
Safety and efficacy of pridopidine in patients with Huntington's disease (PRIDE-HD): a phase 2, randomised, placebo-controlled, multicentre, dose-ranging study Ralf Reilmann, Andrew McGarry, Igor D. Grachev, The Lancet Neurology Neurodegenerative DiseasesMedicinePsychotropic MedicationPsychopharmacologyPharmacotherapy	2018	104
Novel neuro-audiological findings and further evidence for TWNK involvement in Perrault syndrome Monika Ołdak, Dominika Oziębło, Agnieszka Pollak, Journal of Translational Medicine	2017	51
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
Two Novel Pathogenic Variants Confirm RMND1 Causative Role in Perrault Syndrome with Renal Involvement Dominika Oziębło, J. Pazik, Iwona Stępniak, Genes	2020	30
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
Pathology of mitochondria in MELAS syndrome: an ultrastructural study Paulina Felczak, Eliza Lewandowska, Iwona Stępniak, Polish Journal of Pathology	2017	11

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