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Gabriela Klodowska-Duda

Researcher at Medical University of Silesia

Publications -  23
Citations -  938

Gabriela Klodowska-Duda is an academic researcher from Medical University of Silesia. The author has contributed to research in topics: Haplotype & Age of onset. The author has an hindex of 15, co-authored 23 publications receiving 785 citations.

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Journal ArticleDOI

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

Davina J. Hensman Moss, +734 more
- 01 Sep 2017 - 
TL;DR: A novel measure of disease progression and a genome-wide significant signal on chromosome 5 spanning three genes: MSH3, DHFR, and MTRNR2L2 is generated, suggesting this mechanism as an area for future therapeutic investigation.
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Safety and efficacy of opicinumab in patients with relapsing multiple sclerosis (SYNERGY): a randomised, placebo-controlled, phase 2 trial

Diego Cadavid, +98 more
- 05 Jul 2019 - 
TL;DR: The findings did not show a significant dose-linear improvement in disability compared with placebo in patients with relapsing multiple sclerosis, and a linear dose-response in the probability of confirmed disability improvement was not seen.
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The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications.

TL;DR: Both nonsynonymous and synonymous SNPs within functional COMT haplotype blocks may be more relevant than individual SNPs in conferring PD susceptibility and this may be useful in instituting individualized therapy for PD patients.
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CARD15 variants in patients with sporadic Parkinson's disease

TL;DR: The results of the study suggest, that the polymorphism in CARD15/NOD2 gene may be a risk factor for sporadic PD development, and support the concept of inflammatory pathogenesis of PD.
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The effect of monoamine oxidase B (MAOB) and catechol‐O‐methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease

TL;DR: The aim of the study was to find out if a relationship exists between MAOB and COMT haplotypes and motor disturbances onset in PD patients treated with levodopa preparations.