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International Journal of Molecular Sciences|October 13, 2021
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALSMarta Lualdi, Adeena Shafique, Edoardo Pedrini, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 27, 2023
Phosphorylated tau in plasma could be a biomarker of lower motor neuron impairment in amyotrophic lateral sclerosisFederico Verde, Ilaria Milone, Eleonora Colombo, et al.Journal of Neurology|October 6, 2023
The value of routine blood work-up in clinical stratification and prognosis of patients with amyotrophic lateral sclerosisFrancesco Gentile, Alessio Maranzano, Federico Verde, et al.Journal of Medical Genetics|October 29, 2009
Mutations of FUS gene in sporadic amyotrophic lateral sclerosisLucia Corrado, Roberto Del Bo, Barbara Castellotti, et al.Neuron|November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALSBradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.Nature Genetics|July 26, 2016
NEK1 variants confer susceptibility to amyotrophic lateral sclerosisKevin P Kenna, Perry T C van Doormaal, Annelot M Dekker, et al.JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.Pageof 5