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S K Marie

Showing results (11-20 of 45) with videos related to

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Journal of Medical Genetics|December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathiesE S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics|May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than femalesM Zatz, S K Marie, A Cerqueira, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|January 1, 1997
Neuroimaging findings in Rasmussen's syndromeE M Yacubian, S K Marie, R M Valério, 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.
Arquivos De Neuro-Psiquiatria|December 6, 2000
Emery-Dreifuss muscular dystrophy: anatomical-clinical correlation (case report)A A Carvalho, J A Levy, P S Gutierrez, 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.
Arquivos De Neuro-Psiquiatria|February 23, 2000
Kearns-Sayre syndrome "plus". Classical clinical findings and dystoniaS K Marie, A A Carvalho, L F Fonseca, et al.
Journal of Child Neurology|June 8, 2001
Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic reportE M Yacubian, S Rosemberg, T L Garrido Neto, et al.
Brain & Development|January 1, 1996
Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiencyU C Reed, S K Marie, M Vainzof, et al.
American Journal of Medical Genetics|August 15, 1994
Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritanceM R Passos-Bueno, S K Marie, M Monteiro, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathiesE S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics|May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than femalesM Zatz, S K Marie, A Cerqueira, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|January 1, 1997
Neuroimaging findings in Rasmussen's syndromeE M Yacubian, S K Marie, R M Valério, 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.
Arquivos De Neuro-Psiquiatria|December 6, 2000
Emery-Dreifuss muscular dystrophy: anatomical-clinical correlation (case report)A A Carvalho, J A Levy, P S Gutierrez, 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.
Arquivos De Neuro-Psiquiatria|February 23, 2000
Kearns-Sayre syndrome "plus". Classical clinical findings and dystoniaS K Marie, A A Carvalho, L F Fonseca, et al.
Journal of Child Neurology|June 8, 2001
Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic reportE M Yacubian, S Rosemberg, T L Garrido Neto, et al.
Brain & Development|January 1, 1996
Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiencyU C Reed, S K Marie, M Vainzof, et al.
American Journal of Medical Genetics|August 15, 1994
Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritanceM R Passos-Bueno, S K Marie, M Monteiro, et al.
Pageof 5