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Neurology|May 5, 1998
Effects of aerobic training in patients with mitochondrial myopathiesT Taivassalo, N De Stefano, Z Argov, et al.
American Journal of Medical Genetics|September 19, 1997
Type I Gaucher disease due to homozygosity for the 259T mutation in a Bedouin patientR Rockah, R Narinsky, L Hatskelzon, et al.
Biochimica Et Biophysica Acta|January 4, 1978
Inhibition of conjugation in Tetrahymena pyriformis by cerulenin. Possible requirement for de novo lipid synthesisA Frisch, A Loyter, R Levy, et al.
Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.
Muscle & Nerve|October 27, 1997
Biochemical and genetic studies in a family with mitochondrial myopathyT D Heiman-Patterson, Z Argov, J M Chavin, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13I Eisenberg, H Hochner, M Shemesh, et al.
American Journal of Medical Genetics|April 15, 2000
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammationE M McNally, C T Ly, H Rosenmann, et al.
Neurology|August 19, 2007
GNE protein expression and subcellular distribution are unaltered in HIBMS Krause, A Aleo, S Hinderlich, et al.
Human Mutation|January 1, 1997
Molecular basis of heat labile hexosaminidase B among Jews and ArabsG Narkis, A Adam, L Jaber, et al.
Israel Journal of Medical Sciences|December 1, 1976
Tay-Sachs disease in a Moroccan Jewish family: a possible new mutationG Bach, R Navon, M Zeigler, et al.
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