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Works
11
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Extensive genetics of ALS: a population-based study in Italy
Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD
Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels
Dealing with Data Scarcity in Rare Diseases: Dynamic Bayesian Networks and Transfer Learning to Develop Prognostic Models of Amyotrophic Lateral Sclerosis
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis in Sardinia, insular Italy, 1995-2009
Exome sequencing reveals VCP mutations as a cause of familial ALS
Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations.
Differential neuropsychological profile of ALS patients with and without C9orf72 mutation
