Last Posted: Jul 09, 2020
- SOD1 Suppression with Adeno-Associated Virus and MicroRNA in Familial ALS.
Mueller Christian et al. The New England journal of medicine 2020 Jul (2) 151-158 - Phase 1-2 Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS.
Miller Timothy et al. The New England journal of medicine 2020 Jul (2) 109-119 - The Beginning of Genomic Therapies for ALS.
Hardiman Orla et al. The New England journal of medicine 2020 Jul (2) 180-181 - Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort.
Scarlino Stefania et al. International journal of molecular sciences 2020 May 21(9) - Prevalence of C9orf72 hexanucleotide repeat expansion in Greek patients with sporadic ALS.
Sokratous Maria et al. Amyotrophic lateral sclerosis & frontotemporal degeneration 2020 Apr 1-3 - Molecular analysis and clinical diversity of distal hereditary motor neuropathy.
Liu Xiaoxuan et al. European journal of neurology 2020 Apr - Prediction of caregiver burden in amyotrophic lateral sclerosis: a machine learning approach using random forests applied to a cohort study.
Antoniadi Anna Markella et al. BMJ open 2020 Feb 10(2) e033109 - Hereditary Motor Neuropathies and Amyotrophic Lateral Sclerosis: a Molecular and Clinical Update.
Garcia-Santibanez Rocio et al. Current neurology and neuroscience reports 2018 18(12) 93 - CMS-01 Genetic testing for familial amyotrophic lateral sclerosis (ALS): insights and challenges.
Crook Ashley et al. Amyotrophic lateral sclerosis & frontotemporal degeneration 2019 Nov 20(sup1) 327-347 - NIH's All of Us Partners with HudsonAlpha on Long-Read Sequencing Project
Clinical Omics, October 18, 2019
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