Robert Brown
Robert Brown
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Cited by
Cited by
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
DR Rosen, T Siddique, D Patterson, DA Figlewicz, P Sapp, A Hentati, ...
Nature 362 (6415), 59-62, 1993
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
TJ Kwiatkowski Jr, DA Bosco, AL Leclerc, E Tamrazian, CR Vanderburg, ...
Science 323 (5918), 1205-1208, 2009
Adams and Victor's principles of neurology
AH Ropper, RH Brown
Adams and Victor's principles of neurology, 1382-1382, 2005
Amyotrophic lateral sclerosis
RH Brown, A Al-Chalabi
New England Journal of Medicine 377 (2), 162-172, 2017
Decoding ALS: from genes to mechanism
JP Taylor, RH Brown Jr, DW Cleveland
Nature 539 (7628), 197-206, 2016
Tocilizumab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
RECOVERY Collaborative Group
Lancet (London, England) 397 (10285), 1637, 2021
Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury
AG Reaume, JL Elliott, EK Hoffman, NW Kowall, RJ Ferrante, DR Siwek, ...
Nature genetics 13 (1), 43-47, 1996
Molecular biology of amyotrophic lateral sclerosis: insights from genetics
P Pasinelli, RH Brown
Nature Reviews Neuroscience 7 (9), 710-723, 2006
Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice
AM Clement, MD Nguyen, EA Roberts, ML Garcia, S Boillee, M Rule, ...
science 302 (5642), 113-117, 2003
Mutant dynactin in motor neuron disease
I Puls, C Jonnakuty, BH LaMonte, ELF Holzbaur, M Tokito, E Mann, ...
Nature genetics 33 (4), 455-456, 2003
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
J Liu, M Aoki, I Illa, C Wu, M Fardeau, C Angelini, C Serrano, ...
Nature genetics 20 (1), 31-36, 1998
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy
EP Hoffman, KH Fischbeck, RH Brown, M Johnson, R Medori, JD Loire, ...
New England Journal of Medicine 318 (21), 1363-1368, 1988
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
Science 347 (6229), 1436-1441, 2015
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
S Hadano, CK Hand, H Osuga, Y Yanagisawa, A Otomo, RS Devon, ...
Nature genetics 29 (2), 166-173, 2001
Insulin-regulatable tissues express a unique insulin-sensitive glucose transport protein
DE James, R Brown, J Navarro, PF Pilch
Nature 333 (6169), 183-185, 1988
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
MJ Greenway, PM Andersen, C Russ, S Ennis, S Cashman, C Donaghy, ...
Nature genetics 38 (4), 411-413, 2006
Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS
DA Bosco, G Morfini, NM Karabacak, Y Song, F Gros-Louis, P Pasinelli, ...
Nature neuroscience 13 (11), 1396-1403, 2010
Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity.
DR Borchelt, MK Lee, HS Slunt, M Guarnieri, ZS Xu, PC Wong, ...
Proceedings of the National Academy of Sciences 91 (17), 8292-8296, 1994
Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons
BJ Wainger, E Kiskinis, C Mellin, O Wiskow, SSW Han, J Sandoe, ...
Cell reports 7 (1), 1-11, 2014
Epidemiology of mutations in superoxide dismutase in amyotrophic lateal sclerosis
ME Cudkowicz, D McKenna‐Yasek, PE Sapp, W Chin, B Geller, ...
Annals of Neurology: Official Journal of the American Neurological …, 1997
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