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

B T Darras

Showing results (41-50 of 55) with videos related to

Pageof 6
Sort By:
Pediatric Cardiology|September 22, 2007
Safety and efficacy of carvedilol therapy for patients with dilated cardiomyopathy secondary to muscular dystrophyJ Rhodes, R Margossian, B T Darras, et al.
Journal of Child Neurology|July 17, 2001
Magnetic resonance spectroscopy and magnetic resonance imaging findings in Krabbe's diseaseM K Zarifi, A A Tzika, L G Astrakas, et al.
American Journal of Medical Genetics|July 23, 1998
Exclusion of the gastrin-releasing peptide receptor (GRPR) locus as a candidate gene for Rett syndromeG Heidary, L L Hampton, N C Schanen, et al.
Genomics|March 1, 1990
The gene for the RNA component of the mitochondrial RNA-processing endoribonuclease is located on human chromosome 9p and on mouse chromosome 4C L Hsieh, T A Donlon, B T Darras, et al.
Genomics|April 1, 1988
Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32M Zeviani, B T Darras, R Rizzuto, et al.
Neurology|July 13, 2006
A novel mutation in two families with limb-girdle muscular dystrophy type 2CD R Duncan, P B Kang, J C Rabbat, et al.
Neuromuscular Disorders : NMD|January 22, 2002
Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profileC G Bönnemann, J Wong, K J Jones, et al.
American Journal of Human Genetics|March 1, 1987
Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletionsU Francke, J F Harper, B T Darras, et al.
Neurology|April 18, 2007
Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutationM P Gorman, M R Golomb, L E Walsh, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathyC G Bönnemann, G F Cox, F Shapiro, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Pediatric Cardiology|September 22, 2007
Safety and efficacy of carvedilol therapy for patients with dilated cardiomyopathy secondary to muscular dystrophyJ Rhodes, R Margossian, B T Darras, et al.
Journal of Child Neurology|July 17, 2001
Magnetic resonance spectroscopy and magnetic resonance imaging findings in Krabbe's diseaseM K Zarifi, A A Tzika, L G Astrakas, et al.
American Journal of Medical Genetics|July 23, 1998
Exclusion of the gastrin-releasing peptide receptor (GRPR) locus as a candidate gene for Rett syndromeG Heidary, L L Hampton, N C Schanen, et al.
Genomics|March 1, 1990
The gene for the RNA component of the mitochondrial RNA-processing endoribonuclease is located on human chromosome 9p and on mouse chromosome 4C L Hsieh, T A Donlon, B T Darras, et al.
Genomics|April 1, 1988
Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32M Zeviani, B T Darras, R Rizzuto, et al.
Neurology|July 13, 2006
A novel mutation in two families with limb-girdle muscular dystrophy type 2CD R Duncan, P B Kang, J C Rabbat, et al.
Neuromuscular Disorders : NMD|January 22, 2002
Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profileC G Bönnemann, J Wong, K J Jones, et al.
American Journal of Human Genetics|March 1, 1987
Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletionsU Francke, J F Harper, B T Darras, et al.
Neurology|April 18, 2007
Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutationM P Gorman, M R Golomb, L E Walsh, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathyC G Bönnemann, G F Cox, F Shapiro, et al.
Pageof 6