Last Posted: Sep 21, 2019
- ALS gene may be a hitchhiker’s guide to the neuron
NIH, September 19, 2019 - Mutations in the SPTLC1 gene are a cause of amyotrophic lateral sclerosis that may be amenable to serine supplementation
JO Johnson et al, BioRXIV, September 19, 2019 - Genetic testing in fetuses with isolated agenesis of the corpus callosum.
She Qin et al. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2019 Aug 1-201 - Update on amyotrophic lateral sclerosis genetics.
Brenner David et al. Current opinion in neurology 2019 Jul - Lifetime Risk and Heritability of Amyotrophic Lateral Sclerosis.
Ryan Marie et al. JAMA neurology 2019 Jul - The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public.
van der Spek Rick A A et al. Amyotrophic lateral sclerosis & frontotemporal degeneration 2019 Aug 20(5-6) 432-440 - Rare variants in MYH15 modify amyotrophic lateral sclerosis risk
Kin H. et al. Human Molecular Genetics, Volume 28, Issue 14, 15 July 2019, Pages 2309?2318 - Adjusted Cost Analysis of Video Televisits for the Care of People with ALS.
Paganoni Sabrina et al. Muscle & nerve 2019 May - Nutritional counseling with or without mobile health technology: a randomized open-label standard-of-care-controlled trial in ALS.
Wills Anne Marie et al. BMC neurology 2019 May 19(1) 104 - An update on genetic frontotemporal dementia.
Greaves Caroline V et al. Journal of neurology 2019 May
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