Associated Papers
Bridging pleiotropic mechanisms in leprosy type-1 reactions and neurodegenerative diseases.
Fava VM et al.
Scientific Reports, 2025
41430073 (PubMed )
Supplement: 41598_2025_30734_MOESM2_ESM.xlsx › Variants
Comprehensive genetic screening of the South African Parkinson's disease study collection using the NeuroBooster array.
Step K et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
41445612 (PubMed )
Supplement: media-1.pdf
Whole-Genome Sequencing Reveals a Novel GATA2 Mutation in Lower-Grade Glioma: Bioinformatics Analysis of Functional and Therapeutic Implications.
Handoko et al.
Cancers, 2025
41154393 (PubMed )
Supplement: cancers-17-03338-s001.zip › Table_S1._SNV_Analysis.xlsx › SNV_Analysis
Refractory erythroderma in idiopathic hypereosinophilic syndrome: A case treated with mepolizumab and abrocitinib.
Elhaj H et al.
Sage Open Medical Case Reports, 2025
HTRA2 variations in Taiwanese Parkinson's disease.
Chen CM et al.
Journal of Neural Transmission (vienna, Austria : 1996), 2014
Genetic variations of Omi/HTRA2 in Chinese patients with Parkinson's disease.
Wang CY et al.
Brain Research, 2011
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