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Cytogenetic and Genome Research|November 20, 2002
Establishment of the genomic structure and identification of thirteen single-nucleotide polymorphisms in the human RECK geneI Eisenberg, H Hochner, M Sadeh, et al.Archives of Neurology|November 1, 1980
Congenital myotonic dystrophy: fiber type abnormalities in two casesZ Argov, D Gardner-Medwin, M A Johnson, et al.Annals of Neurology|September 1, 1988
Hexosaminidase A deficiency manifesting as spinal muscular atrophy of late onsetA Karni, R Navon, M SadehClinical Chemistry|July 1, 1978
Hexosaminidase A in amniotic fluid of Tay-Sachs fetusesB Geiger, R Navon, R ArnonCellular Immunology|August 1, 1994
Fine specificity of T cell lines and clones that are capable of inducing autoimmune manifestations in miceS L Kirshner, Y Katz-Levy, I Wirguin, et al.Neurology|June 1, 1987
Familial progressive neuronal disease and chronic idiopathic intestinal pseudo-obstructionI Steiner, A Steinberg, Z Argov, et al.Annals of Neurology|July 1, 1987
Muscle energy metabolism in human phosphofructokinase deficiency as recorded by 31P nuclear magnetic resonance spectroscopyZ Argov, W J Bank, J Maris, et al.Archives of Neurology|June 1, 1987
Phosphorus magnetic resonance spectroscopy of partially blocked muscle glycolysis. An in vivo study of phosphoglycerate mutase deficiencyZ Argov, W J Bank, B Boden, et al.The Journal of Clinical Investigation|June 1, 1988
Effects of thyroid hormones on skeletal muscle bioenergetics. In vivo phosphorus-31 magnetic resonance spectroscopy study of humans and ratsZ Argov, P F Renshaw, B Boden, et al.American Journal of Human Genetics|August 1, 1992
Identification and rapid detection of three Tay-Sachs mutations in the Moroccan Jewish populationL Drucker, R L Proia, R NavonPageof 22