R. Brown

Inflammation in dysferlin myopathy: Immunohistochemical characterization of 13 patients

R. Rojas-García, I. Illa, E. Gallardo, 2001, Neurology.

Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis

Robert H. Brown, D. A. Bosco, C. Shaw, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Tau levels do not influence human ALS or motor neuron degeneration in the SOD1G93A mouse

A. Goris, B. Dubois, S. Boonen, 2010, Neurology.

Dysferlin is a surface membrane–associated protein that is absent in Miyoshi myopathy

Y. Hayashi, K. Arahata, R H Brown, 1999, Neurology.

Calpain-3 and dysferlin protein screening in patients with limb–girdle dystrophy and myopathy

C. Angelini, E. Pegoraro, M. Fanin, 2001, Neurology.

Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22

J. Haines, D. McKenna-Yasek, B. Hosler, 1999, Neurology.

Dysferlin mutations in Japanese Miyoshi myopathy

Y. Itoyama, I. Nonaka, Kayoko Saito, 2003, Neurology.

Mice lacking cytosolic copper/zinc superoxide dismutase display a distinctive motor axonopathy

J. Shefner, D. Flood, A. Reaume, 1999, Neurology.

Disease course unaltered by a single intracisternal injection of BMP‐7 in ALS mice

M. Cudkowicz, P. Kaplan, E. Smith, 2002, Muscle and Nerve.