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M Zatz

Showing results (161-170 of 252) with videos related to

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Neuromuscular Disorders : NMD|December 9, 2003
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.
American Journal of Human Genetics|July 1, 1997
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12E S Moreira, M Vainzof, S K Marie, et al.
Human Heredity|January 1, 1991
Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophiesE Rabbi-Bortolini, G M Dal Colletto, M R Passos-Bueno, et al.
Journal of Clinical Ultrasound : JCU|March 1, 1975
Real-time imaging with a new ultrasonic camera: part II, preliminary studies in normal adultsL M Zatz, E W Marich, P S Green, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|February 4, 2015
Stem cells for amyotrophic lateral sclerosis modeling and therapy: myth or fact?G C Coatti, M S Beccari, T R Olávio, et al.
Archives of General Psychiatry|July 1, 1988
Computed tomographic evidence for generalized sulcal and ventricular enlargement in schizophreniaA Pfefferbaum, R B Zipursky, K O Lim, et al.
Journal of the Neurological Sciences|June 29, 1999
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationM Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Academic Radiology|September 16, 2008
Discordance rates between preliminary and final radiology reports on cross-sectional imaging studies at a level 1 trauma centerKathryn J Stevens, Karen L Griffiths, Jarrett Rosenberg, et al.
American Journal of Medical Genetics|April 17, 1998
Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosisE Rabbi-Bortolini, A L Bernardino, A L Lopes, et al.
American Journal of Medical Genetics|January 1, 1991
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequenceM R Passos-Bueno, J Terwilliger, J Ott, et al.
Pageof 26

Showing results (161-170 of 252) with videos related to

Sort By:
Pageof 26
Neuromuscular Disorders : NMD|December 9, 2003
Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.
American Journal of Human Genetics|July 1, 1997
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12E S Moreira, M Vainzof, S K Marie, et al.
Human Heredity|January 1, 1991
Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophiesE Rabbi-Bortolini, G M Dal Colletto, M R Passos-Bueno, et al.
Journal of Clinical Ultrasound : JCU|March 1, 1975
Real-time imaging with a new ultrasonic camera: part II, preliminary studies in normal adultsL M Zatz, E W Marich, P S Green, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|February 4, 2015
Stem cells for amyotrophic lateral sclerosis modeling and therapy: myth or fact?G C Coatti, M S Beccari, T R Olávio, et al.
Archives of General Psychiatry|July 1, 1988
Computed tomographic evidence for generalized sulcal and ventricular enlargement in schizophreniaA Pfefferbaum, R B Zipursky, K O Lim, et al.
Journal of the Neurological Sciences|June 29, 1999
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationM Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Academic Radiology|September 16, 2008
Discordance rates between preliminary and final radiology reports on cross-sectional imaging studies at a level 1 trauma centerKathryn J Stevens, Karen L Griffiths, Jarrett Rosenberg, et al.
American Journal of Medical Genetics|April 17, 1998
Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosisE Rabbi-Bortolini, A L Bernardino, A L Lopes, et al.
American Journal of Medical Genetics|January 1, 1991
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequenceM R Passos-Bueno, J Terwilliger, J Ott, et al.
Pageof 26