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Neuromolecular Medicine|October 5, 2020
Low Levels of LRRK2 Gene Expression are Associated with LRRK2 SNPs and Contribute to Parkinson's Disease ProgressionSelma Yılmazer, Esin Candaş, Gençer Genç, et al.The International Journal of Neuroscience|September 17, 2020
Genetic variants of vitamin D metabolism-related <i>DHCR7/NADSYN1</i> locus and <i>CYP2R1</i> gene are associated with clinical features of Parkinson's diseaseMerve Alaylıoğlu, Erdinç Dursun, Gençer Genç, et al.Neuromolecular Medicine|June 11, 2016
GC and VDR SNPs and Vitamin D Levels in Parkinson's Disease: The Relevance to Clinical FeaturesDuygu Gezen-Ak, Merve Alaylıoğlu, Gençer Genç, et al.Journal of Alzheimer'S Disease : JAD|February 3, 2020
Altered Transcriptional Profile of Mitochondrial DNA-Encoded OXPHOS Subunits, Mitochondria Quality Control Genes, and Intracellular ATP Levels in Blood Samples of Patients with Parkinson's DiseaseDuygu Gezen-Ak, Merve Alaylıoğlu, Gençer Genç, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 24, 2021
The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical PracticeAtay Vural, Gülşah Şimşir, Şeyma Tekgül, et al.Plos One|October 3, 2023
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease ProjectEva-Juliane Vollstedt, Harutyun Madoev, Anna Aasly, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 24, 2023
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD CohortEva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, et al.Brain : a Journal of Neurology|August 1, 2024
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease studyAna Westenberger, Volha Skrahina, Tatiana Usnich, et al.Pageof 2