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Clinica Chimica Acta; International Journal of Clinical Chemistry|March 4, 1999
Distribution of serum creatine kinase activity in young healthy personsE I Lev, I Tur-Kaspa, I Ashkenazy, et al.Neurology|May 14, 2003
Hereditary inclusion body myopathy: the Middle Eastern genetic clusterZ Argov, I Eisenberg, G Grabov-Nardini, et al.Journal of Phonetics|March 29, 2016
Velar-vowel coarticulation in a virtual target model of stop productionStefan A Frisch, Sylvie M WodzinskiHuman Genetics|May 1, 1996
A new point mutation affecting the fourth transmembrane domain of PMP22 results in severe de novo Charcot-Marie-Tooth diseaseR Navon, B Seifried, N S Gal-On, et al.American Journal of Human Genetics|July 1, 1976
Low levels of beta hexosaminidase A in healthy individuals with apparent deficiency of this enzymeR Navon, B Geiger, Y B Yoseph, et al.Journal of Applied Behavior Analysis|January 1, 1974
Training generalized receptive prepositions in retarded childrenS A Frisch, J B SchumakerThe British Journal of Psychiatry : the Journal of Mental Science|September 1, 1988
Post-partum psychosis in adult GM2 gangliosidosis. A case reportP Lichtenberg, R Navon, E Wertman, et al.Journal of Medical Genetics|June 1, 1983
Intestinal obstruction and cystic fibrosis: antenatal ultrasound appearanceJ Shalev, R Navon, D Urbach, et al.Annals of Neurology|November 1, 1991
Hereditary branching enzyme dysfunction in adult polyglucosan body disease: a possible metabolic cause in two patientsA Lossos, V Barash, D Soffer, et al.Journal of Neurology|April 29, 2008
Increased severity over generations of Charcot-Marie-Tooth disease type 1AI Steiner, M Gotkine, B Steiner-Birmanns, et al.Pageof 22