Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

78 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Scoring Algorithm-Based Genomic Testing in Dystonia: A Prospective Validation Study.
Zech M, Jech R, Boesch S, Škorvánek M, Necpál J, Švantnerová J, Wagner M, Sadr-Nabavi A, Distelmaier F, Krenn M, Serranová T, Rektorová I, Havránková P, Mosejová A, Příhodová I, Šarláková J, Kulcsarová K, Ulmanová O, Bechyně K, Ostrozovičová M, Haň V, Ventosa JR, Brunet T, Berutti R, Shariati M, Shoeibi A, Schneider SA, Kuster A, Baumann M, Weise D, Wilbert F, Janzarik WG, Eckenweiler M, Mall V, Haslinger B, Berweck S, Winkelmann J, Oexle K. Zech M, et al. Among authors: shoeibi a. Mov Disord. 2021 Aug;36(8):1959-1964. doi: 10.1002/mds.28614. Epub 2021 May 5. Mov Disord. 2021. PMID: 33949708
Clinically relevant copy-number variants in exome sequencing data of patients with dystonia.
Zech M, Boesch S, Škorvánek M, Necpál J, Švantnerová J, Wagner M, Dincer Y, Sadr-Nabavi A, Serranová T, Rektorová I, Havránková P, Ganai S, Mosejová A, Příhodová I, Šarláková J, Kulcsarová K, Ulmanová O, Bechyně K, Ostrozovičová M, Haň V, Ventosa JR, Shariati M, Shoeibi A, Weber S, Mollenhauer B, Trenkwalder C, Berutti R, Strom TM, Ceballos-Baumann A, Mall V, Haslinger B, Jech R, Winkelmann J. Zech M, et al. Among authors: shoeibi a. Parkinsonism Relat Disord. 2021 Mar;84:129-134. doi: 10.1016/j.parkreldis.2021.02.013. Epub 2021 Feb 12. Parkinsonism Relat Disord. 2021. PMID: 33611074
AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonism.
Garavaglia B, Vallian S, Romito LM, Straccia G, Capecci M, Invernizzi F, Andrenelli E, Kazemi A, Boesch S, Kopajtich R, Olfati N, Shariati M, Shoeibi A, Sadr-Nabavi A, Prokisch H, Winkelmann J, Zech M. Garavaglia B, et al. Among authors: shoeibi a. Parkinsonism Relat Disord. 2022 Apr;97:52-56. doi: 10.1016/j.parkreldis.2022.03.007. Epub 2022 Mar 16. Parkinsonism Relat Disord. 2022. PMID: 35306330
Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease.
Seyedtaghia MR, Soudyab M, Shariati M, Esfehani RJ, Vafadar S, Shalaei N, Nouri V, Zech M, Winkelmann J, Shoeibi A, Sadr-Nabavi A. Seyedtaghia MR, et al. Among authors: shoeibi a. Heliyon. 2023 Apr 8;9(4):e15393. doi: 10.1016/j.heliyon.2023.e15393. eCollection 2023 Apr. Heliyon. 2023. PMID: 37095917 Free PMC article.
Diplopia in Progressive Supranuclear Palsy.
Yazdi N, Ghamsari MR, Shoeibi A, Rohani M. Yazdi N, et al. Among authors: shoeibi a. Mov Disord Clin Pract. 2020 Jan 22;7(2):232-233. doi: 10.1002/mdc3.12890. eCollection 2020 Feb. Mov Disord Clin Pract. 2020. PMID: 32071947 Free PMC article. No abstract available.
Progress in the treatment of Parkinson-Plus syndromes.
Olfati N, Shoeibi A, Litvan I. Olfati N, et al. Among authors: shoeibi a. Parkinsonism Relat Disord. 2019 Feb;59:101-110. doi: 10.1016/j.parkreldis.2018.10.006. Epub 2018 Oct 3. Parkinsonism Relat Disord. 2019. PMID: 30314846 Review.
78 results