Publications by authors named "Maria Rakowicz"

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Frequently observed polyneuropathy expands phenotypic spectrum of apparently pure autosomal dominant hereditary spastic paraplegias.
Iwona Stępniak, Maria Rakowicz, Wanda Lipczyńska-Łojkowska, Anna Sobańska, Ewelina Elert-Dobkowska

Neurol Neurochir Pol· July 2025

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Quantitative Evaluation of Stance as a Sensitive Biomarker of Postural Ataxia Development in Preclinical SCA1 Mutation Carriers.
Anna Sobanska, Leszek Czerwosz, Anna Sulek, Rafal Rola, Iwona Stepniak, Maria Rakowicz

Cerebellum· October 2024

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Levels of Neurofilament Light at the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 1.
Carlo Wilke, David Mengel, Ludger Schöls, Holger Hengel, Maria Rakowicz

Neurology· May 2022

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Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study.
Heike Jacobi, Sophie Tezenas du Montcel, Sandro Romanzetti, Florian Harmuth, Caterina Mariotti, Maria Rakowicz

Lancet Neurol· September 2020

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Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice.
Carlo Wilke, Eva Haas, Kathrin Reetz, Jennifer Faber, Hector Garcia-Moreno, Maria Rakowicz

EMBO Mol Med· July 2020

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Prediction of Survival With Long-Term Disease Progression in Most Common Spinocerebellar Ataxia.
Alhassane Diallo, Heike Jacobi, Arron Cook, Paola Giunti, Michael H Parkinson, Maria Rakowicz

Mov Disord· August 2019

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Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.
Anna Sulek, Anna Lusakowska, Wioletta Krysa, Marta Rajkiewicz, Anna Kaminska, Maria Rakowicz

Neurol Neurochir Pol· June 2019

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Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes.
Ewelina Elert-Dobkowska, Iwona Stepniak, Wioletta Krysa, Karolina Ziora-Jakutowicz, Maria Rakowicz

Neurogenetics· March 2019

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Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias.
Heike Jacobi, Sophie Tezenas du Montcel, Peter Bauer, Paola Giunti, Arron Cook, Maria Rakowicz

J Neurol· September 2018

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Are there clinical and neurophysiologic predictive factors for a positive response to HF-rTMS in patients with treatment-resistant depression?
Anna Poleszczyk, Maria Rakowicz, Tadeusz Parnowski, Jakub Antczak, Łukasz Święcicki

Psychiatry Res· June 2018

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WITHDRAWN: Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.
Anna Sulek, Anna Lusakowska, Wioletta Krysa, Marta Rajkiewicz, Anna Kaminska, Maria Rakowicz

Neurol Neurochir Pol· May 2018

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Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study.
Alhassane Diallo, Heike Jacobi, Arron Cook, Robyn Labrum, Alexandra Durr, Maria Rakowicz

Lancet Neurol· April 2018

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The influence of the repetitive transcranial magnetic stimulation on sleep quality in depression.
Jakub Maria Antczak, Anna Poleszczyk, Adam Wichniak, Maria Rakowicz, Tadeusz Jerzy Parnowski

Psychiatr Pol· October 2017

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Body Mass Index Decline Is Related to Spinocerebellar Ataxia Disease Progression.
Alhassane Diallo, Heike Jacobi, Tanja Schmitz-Hübsch, Arron Cook, Robyn Labrum, Maria Rakowicz

Mov Disord Clin Pract· August 2017

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High relative frequency of SCA1 in Poland reflecting a potential founder effect.
Wioletta Krysa, Anna Sulek, Maria Rakowicz, Walentyna Szirkowiec, Jacek Zaremba

Neurol Sci· August 2016

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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 Stepniak, Wioletta Krysa, Marta Rajkiewicz, Maria Rakowicz

J Neurol Sci· December 2015

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Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
Heike Jacobi, Sophie Tezenas du Montcel, Peter Bauer, Paola Giunti, Arron Cook, Maria Rakowicz

Lancet Neurol· November 2015

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Morphological changes of skeletal muscle in spinal and bulbar muscular atrophy (SBMA), Kennedy's disease: a case report.
Albert Acewicz, Teresa Wierzba-Bobrowicz, Eliza Lewandowska, Halina Sienkiewicz-Jarosz, Anna Sulek, Maria Rakowicz

Clin Neuropathol· August 2015

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Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
Sophie Tezenas du Montcel, Alexandra Durr, Peter Bauer, Karla P Figueroa, Yaeko Ichikawa, Maria Rakowicz

Brain· September 2014

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Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6.
Sophie Tezenas du Montcel, Alexandra Durr, Maria Rakowicz, Lorenzo Nanetti, Perrine Charles

J Med Genet· July 2014

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Negative influence of L-dopa on subjectively assessed sleep but not on nocturnal polysomnography in Parkinson's disease.
Jakub M Antczak, Maria J Rakowicz, Marta Banach, Mirosława Derejko, Jakub Sienkiewicz

Pharmacol Rep· April 2014

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The personal experience of parenting a child with juvenile Huntington's disease: perceptions across Europe.
Virginia Eatough, Helen Santini, Christine Eiser, Marie-Louise Goller, Wioletta Krysa, Maria Rakowicz

Eur J Hum Genet· October 2013

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Corticomotor excitability in drug-naive patients with Parkinson disease.
Mirosława Derejko, Maria Rakowicz, Jakub Antczak, Ewa Inglot, Maria Niewiadomska

Neurol Neurochir Pol· August 2013

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Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Heike Jacobi, Kathrin Reetz, Sophie Tezenas du Montcel, Peter Bauer, Caterina Mariotti, Maria Rakowicz

Lancet Neurol· July 2013

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Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
Kathrin Reetz, Ana S Costa, Shahram Mirzazade, Anna Lehmann, Agnes Juzek, Maria Rakowicz

Brain· March 2013

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