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Neurology|August 1, 1992
Intrafamilial heterogeneity in hereditary motor neuron diseaseJ S Appelbaum, R P Roos, E F Salazar-Grueso, et al.Australian Paediatric Journal|January 1, 1988
Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.Neuroepidemiology|June 7, 2003
A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosisHatice Aksoy, Geoffrey Dean, Marta Elian, et al.Journal of Neurophysiology|March 7, 2014
Effect of fluoxetine on disease progression in a mouse model of ALSJ E Koschnitzky, K A Quinlan, T J Lukas, et al.Science (New York, N.Y.)|June 17, 1994
Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutationM E Gurney, H Pu, A Y Chiu, et al.Yi Chuan Xue Bao = Acta Genetica Sinica|July 2, 1998
[Localization of the gene for 4 hereditary multiple exostoses families]Y Tang, J H Xia, J N Zhou, et al.Neurology|January 1, 1985
Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free dietV Askanas, W K Engel, H H Kwan, et al.Human Molecular Genetics|August 1, 1994
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneityA Hentati, M A Pericak-Vance, W Y Hung, et al.American Journal of Medical Genetics|October 1, 1987
Chorea-acanthocytosis: a report of three new families and implications for genetic counsellingJ M Vance, M A Pericak-Vance, M H Bowman, et al.Genomics|August 1, 1988
The poliovirus sensitivity (PVS) gene is on chromosome 19q12----q13.2T Siddique, R McKinney, W Y Hung, et al.Pageof 11