Familial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes-Reference-Cited by-同舟云学术

Familial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes

Published:2016-11 Issue:46 Volume:95 Page:e5398
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Bartonikova Tereza,Mensikova Katerina,Mikulicova Lenka,Vodicka Radek,Vrtel Radek,Godava Marek,Vastik Miroslav,Kaiserova Michaela,Otruba Pavel,Dolinova Iva,Nevrly Martin,Kanovsky Petr

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference24 articles.

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3. Familial, autosomal-dominant neurodegenerative parkinsonism with cognitive deterioration spanning five generations in a genetically isolated population of south-eastern Moravia, Czech Republic;Mensikova;Biomed Pap Med Fac Univ Palacky Olomouc Czech Rep,2016

4. Monogenic Parkinson's disease and parkinsonism: clinical phenotypes and frequencies of known mutations;Puschmann;Park Relat Disord,2013

5. The phenotypic spectrum of progressive supranuclear palsy;Respondek;Park Relat Disord,2016

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1. Study of an FBXO7 patient mutation reveals Fbxo7 and PI31 co‐regulate proteasomes and mitochondria;The FEBS Journal;2024-03-11

2. Study of an FBXO7 patient mutation reveals Fbxo7 and PI31 co-regulate proteasomes and mitochondria;2021-12-23

3. VPS35, the core component of the retromer complex, and Parkinson's disease;Ibrain;2021-12

4. Mechanisms of VPS35-mediated neurodegeneration in Parkinson's disease;International Review of Movement Disorders;2021

5. Evaluating Basic Next-Generation Sequencing Parameters in Relation to True/False Positivity Findings of Rare Variants in an Isolated Population from the Czech Republic South-Eastern Moravia Region with a High Incidence of Parkinsonism;Bioinformatics and Biomedical Engineering;2020