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M Zatz

Showing results (111-120 of 252) with videos related to

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Journal of Medical Genetics|December 1, 1981
Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locusM Zatz, A M Vianna-Morgante, P Campos, et al.
Archives of General Psychiatry|July 1, 1982
Computed tomography in schizophrenics and normal volunteers. I. Fluid volumeT L Jernigan, L M Zatz, J A Moses, et al.
Neuromuscular Disorders : NMD|November 23, 2006
Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2IN M Vieira, D Schlesinger, F de Paula, et al.
Journal of Molecular Neuroscience : MN|July 9, 2008
The genetics of Alzheimer's disease in Brazil: 10 years of analysis in a unique populationJ R M Oliveira, A L Nishimura, R R Lemos, et al.
Biochemical Pharmacology|March 1, 1982
Nonpolar lipid methylation-identification of nonpolar methylated products synthesized by rat basophilic leukemia cells, retina and parotidY Kloog, M Zatz, B Rivnay, et al.
Archives of General Psychiatry|July 1, 1982
Computed tomography in schizophrenics and normal volunteers. II. Cranial asymmetryT L Jernigan, L M Zatz, J A Moses, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 1, 1981
Separation and characterization of two component tumor lines within the AKR lymphoma, AKTB-1, by fluorescence-activated cell sorting and flow microfluorometry analysis. I. the coexistence of sIg+ and sIg- sublinesM M Zatz, B J Mathieson, C Kanellopoulos-Langevin, et al.
Growth Regulation|March 1, 1991
Short stature in Duchenne muscular dystrophyD Rapaport, G M Colletto, M Vainzof, et al.
Neuropediatrics|August 25, 2001
Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 geneJ S Schwartzman, A Bernardino, A Nishimura, et al.
Neuroradiology|January 1, 1978
Dual kilovoltage at computed tomography: a prereconstruction method for estimation of effective atomic number and electron densityW H Marshall, R Alvarez, A Macovski, et al.
Pageof 26

Showing results (111-120 of 252) with videos related to

Sort By:
Pageof 26
Journal of Medical Genetics|December 1, 1981
Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locusM Zatz, A M Vianna-Morgante, P Campos, et al.
Archives of General Psychiatry|July 1, 1982
Computed tomography in schizophrenics and normal volunteers. I. Fluid volumeT L Jernigan, L M Zatz, J A Moses, et al.
Neuromuscular Disorders : NMD|November 23, 2006
Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2IN M Vieira, D Schlesinger, F de Paula, et al.
Journal of Molecular Neuroscience : MN|July 9, 2008
The genetics of Alzheimer's disease in Brazil: 10 years of analysis in a unique populationJ R M Oliveira, A L Nishimura, R R Lemos, et al.
Biochemical Pharmacology|March 1, 1982
Nonpolar lipid methylation-identification of nonpolar methylated products synthesized by rat basophilic leukemia cells, retina and parotidY Kloog, M Zatz, B Rivnay, et al.
Archives of General Psychiatry|July 1, 1982
Computed tomography in schizophrenics and normal volunteers. II. Cranial asymmetryT L Jernigan, L M Zatz, J A Moses, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 1, 1981
Separation and characterization of two component tumor lines within the AKR lymphoma, AKTB-1, by fluorescence-activated cell sorting and flow microfluorometry analysis. I. the coexistence of sIg+ and sIg- sublinesM M Zatz, B J Mathieson, C Kanellopoulos-Langevin, et al.
Growth Regulation|March 1, 1991
Short stature in Duchenne muscular dystrophyD Rapaport, G M Colletto, M Vainzof, et al.
Neuropediatrics|August 25, 2001
Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 geneJ S Schwartzman, A Bernardino, A Nishimura, et al.
Neuroradiology|January 1, 1978
Dual kilovoltage at computed tomography: a prereconstruction method for estimation of effective atomic number and electron densityW H Marshall, R Alvarez, A Macovski, et al.
Pageof 26