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Ear and Hearing|January 2, 2001
Modeling spoken word recognition performance by pediatric cochlear implant users using feature identificationS A Frisch, D B PisoniMolecular Genetics and Metabolism|April 6, 2010
Two novel exonic point mutations in HEXA identified in a juvenile Tay-Sachs patient: role of alternative splicing and nonsense-mediated mRNA decayA Levit, D Nutman, E Osher, et al.Annals of Neurology|June 1, 1986
Treatment of mitochondrial myopathy due to complex III deficiency with vitamins K3 and C: A 31P-NMR follow-up studyZ Argov, W J Bank, J Maris, et al.Journal of Applied Physiology (Bethesda, Md. : 1985)|February 1, 1992
Substrate regulation of mitochondrial oxidative phosphorylation in hypercapnic rabbit muscleS Nioka, Z Argov, G P Dobson, et al.Clinical Linguistics & Phonetics|February 26, 2016
Anticipatory coarticulation and stability of speech in typically fluent speakers and people who stutterStefan A Frisch, Nathan Maxfield, Alissa BelmontAnnals of Neurology|December 16, 1998
Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme geneA Lossos, Z Meiner, V Barash, et al.Journal of Child Neurology|June 8, 2001
31Phosphorus magnetic resonance spectroscopy in late-onset Tay-Sachs diseaseU Felderhoff-Mueser, J Sperner, P Konstanzcak, et al.Annals of Neurology|April 1, 1997
Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1Z Argov, E Tiram, I Eisenberg, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|November 1, 1994
Transient neurological events during dipyridamole stress test: an arterial steal phenomenon?D Schechter, M Bocher, Y Berlatzky, et al.Neurology|February 1, 1995
Hereditary leukoencephalopathy and palmoplantar keratoderma: a new disorder with increased skin collagen contentA Lossos, H Cooperman, D Soffer, et al.Pageof 22