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Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 20, 2012
A novel TARDBP insertion/deletion mutation in the flail arm variant of amyotrophic lateral sclerosisJennifer A Solski, Shu Yang, Garth A Nicholson, et al.
JAMA Neurology|July 17, 2013
Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G)Marion Simpson, Vanessa Johanssen, Alison Boyd, et al.
Plos One|May 20, 2020
Concentrations of toxic metals and essential trace elements vary among individual neurons in the human locus ceruleusRoger Pamphlett, Rachel Mak, Joonsup Lee, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 10, 2024
Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestryLyndal Henden, Liam G Fearnley, Dean Southwood, et al.
Scientific Reports|June 22, 2022
Association between DNA methylation variability and self-reported exposure to heavy metalsAnna Freydenzon, Marta F Nabais, Tian Lin, et al.
Emerging Infectious Diseases|July 18, 2018
Anncaliia algerae Microsporidial Myositis, New South Wales, AustraliaGaurav Sutrave, Adam Maundrell, Caitlin Keighley, et al.
Croatian Medical Journal|September 1, 2017
Concomitant occurrence of FXTAS and clinically defined sporadic inclusion body myositis: report of two casesMirna Lechpammer, Verónica Martínez Cerdeńo, Michael Ryan Hunsaker, et al.
Molecular Brain|March 8, 2020
A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activityRobin N Stringer, Bohumila Jurkovicova-Tarabova, Sun Huang, et al.
Neurobiology of Aging|May 25, 2022
NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis riskNatalie Grima, Lyndal Henden, Liam G Fearnley, et al.
Neurobiology of Aging|February 14, 2021
Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosisSandrine Chan Moi Fat, Emily P McCann, Kelly L Williams, et al.
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