Maria Rakowicz
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Explore the profile of Maria Rakowicz including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
741
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Recent Articles
1.
Sobanska A, Czerwosz L, Sulek A, Rola R, Stepniak I, Rakowicz M
Cerebellum
. 2024 Mar;
23(5):1882-1891.
PMID: 38492164
The aim of this study was to determine the time between the first detection of postural control impairments and the evident manifestation of ataxia in preclinical SCA1 individuals. Twenty five...
2.
Wilke C, Mengel D, Schols L, Hengel H, Rakowicz M, Klockgether T, et al.
Neurology
. 2022 Mar;
98(20):e1985-e1996.
PMID: 35264424
Background And Objectives: Neurofilament light (NfL) appears to be a promising fluid biomarker in repeat-expansion spinocerebellar ataxias (SCAs), with piloting studies in mixed SCA cohorts suggesting that NfL might be...
3.
Jacobi H, Tezenas du Montcel S, Romanzetti S, Harmuth F, Mariotti C, Nanetti L, et al.
Lancet Neurol
. 2020 Aug;
19(9):738-747.
PMID: 32822634
Background: Spinocerebellar ataxias (SCAs) are autosomal dominant neurodegenerative diseases. Our aim was to study the conversion to manifest ataxia among apparently healthy carriers of mutations associated with the most common...
4.
Wilke C, Haas E, Reetz K, Faber J, Garcia-Moreno H, Santana M, et al.
EMBO Mol Med
. 2020 Jun;
12(7):e11803.
PMID: 32510847
With molecular treatments coming into reach for spinocerebellar ataxia type 3 (SCA3), easily accessible, cross-species validated biomarkers for human and preclinical trials are warranted, particularly for the preataxic disease stage....
5.
Diallo A, Jacobi H, Cook A, Giunti P, Parkinson M, Labrum R, et al.
Mov Disord
. 2019 Jun;
34(8):1220-1227.
PMID: 31211461
Background: Spinocerebellar ataxias are rare dominantly inherited neurodegenerative diseases that lead to severe disability and premature death. Objective: To quantify the impact of disease progression measured by the Scale for...
6.
Elert-Dobkowska E, Stepniak I, Krysa W, Ziora-Jakutowicz K, Rakowicz M, Sobanska A, et al.
Neurogenetics
. 2019 Feb;
20(1):27-38.
PMID: 30778698
Hereditary spastic paraplegias (HSPs) are clinically and genetically heterogeneous neurodegenerative disorders. Numerous genes linked to HSPs, overlapping phenotypes between HSP subtypes and other neurodegenerative disorders and the HSPs' dual mode...
7.
Diallo A, Jacobi H, Schmitz-Hubsch T, Cook A, Labrum R, Durr A, et al.
Mov Disord Clin Pract
. 2018 Oct;
4(5):689-697.
PMID: 30363449
Background: Spinocerebellar ataxias (SCAs) are dominantly inherited, progressive ataxia disorders. Disease progression could be preceded by weight loss. Objectives: We aimed to study the course of weight loss in patients...
8.
Jacobi H, Tezenas du Montcel S, Bauer P, Giunti P, Cook A, Labrum R, et al.
J Neurol
. 2018 Jul;
265(9):2040-2051.
PMID: 29959555
Introduction: To study the long-term evolution of patient-reported outcome measures (PROMs) in the most common spinocerebellar ataxias (SCAs), we analyzed 8 years follow-up data of the EUROSCA Natural History Study,...
9.
Sulek A, Lusakowska A, Krysa W, Rajkiewicz M, Kaminska A, Nojszewska M, et al.
Neurol Neurochir Pol
. 2018 Jun;
PMID: 29880430
The Publisher regrets that this article is an accidental duplication of an article that has already been published, 10.1016/j.pjnns.2018.02.008. The duplicate article has therefore been withdrawn. The full Elsevier Policy...
10.
Poleszczyk A, Rakowicz M, Parnowski T, Antczak J, Swiecicki L
Psychiatry Res
. 2018 Apr;
264:175-181.
PMID: 29649674
Better selection of patients with treatment-resistant depression for high-frequency repetitive transcranial magnetic stimulation (HF-rTMS) would make the procedure more efficient. The objective of this study was to search for clinical...