Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Zatz

Showing results (221-230 of 252) with videos related to

Pageof 26
Sort By:
Molecular and Cellular Probes|October 1, 1995
Molecular characterization of further dystrophin gene microsatellitesS C King, A L Roche, M R Passos-Bueno, et al.
American Journal of Medical Genetics|May 29, 1998
Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophreniaJ R Mendes de Oliveira, P A Otto, H Vallada, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
A Caucasian family with the 3271 mutation in mitochondrial DNAS K Marie, Y Goto, M R Passos-Bueno, et al.
Arquivos De Neuro-Psiquiatria|June 16, 2001
Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17R Nitrini, L S Teixeira da Silva, S Rosemberg, et al.
Journal of Molecular Neuroscience : MN|October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophiesM Vainzof, L V Anderson, E M McNally, et al.
American Journal of Medical Genetics|April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Annals of Neurology|August 1, 1997
Familial spongiform encephalopathy associated with a novel prion protein gene mutationR Nitrini, S Rosemberg, M R Passos-Bueno, et al.
Journal of Child Neurology|April 11, 2000
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical casesU C Reed, S K Marie, M Vainzof, et al.
Revista Do Hospital Das Clinicas|January 10, 2002
Friedreich's ataxia: clinical and molecular study of 25 Brazilian casesL M Albano, M Zatz, C A Kim, et al.
Nature Genetics|February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninE S Moreira, T J Wiltshire, G Faulkner, et al.
Pageof 26

Showing results (221-230 of 252) with videos related to

Sort By:
Pageof 26
Molecular and Cellular Probes|October 1, 1995
Molecular characterization of further dystrophin gene microsatellitesS C King, A L Roche, M R Passos-Bueno, et al.
American Journal of Medical Genetics|May 29, 1998
Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophreniaJ R Mendes de Oliveira, P A Otto, H Vallada, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
A Caucasian family with the 3271 mutation in mitochondrial DNAS K Marie, Y Goto, M R Passos-Bueno, et al.
Arquivos De Neuro-Psiquiatria|June 16, 2001
Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17R Nitrini, L S Teixeira da Silva, S Rosemberg, et al.
Journal of Molecular Neuroscience : MN|October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophiesM Vainzof, L V Anderson, E M McNally, et al.
American Journal of Medical Genetics|April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Annals of Neurology|August 1, 1997
Familial spongiform encephalopathy associated with a novel prion protein gene mutationR Nitrini, S Rosemberg, M R Passos-Bueno, et al.
Journal of Child Neurology|April 11, 2000
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical casesU C Reed, S K Marie, M Vainzof, et al.
Revista Do Hospital Das Clinicas|January 10, 2002
Friedreich's ataxia: clinical and molecular study of 25 Brazilian casesL M Albano, M Zatz, C A Kim, et al.
Nature Genetics|February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninE S Moreira, T J Wiltshire, G Faulkner, et al.
Pageof 26