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S K Marie

Showing results (1-10 of 45) with videos related to

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Pediatric Neurology|July 1, 1994
Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV)S Rosemberg, S K Marie, S Kliemann
Arquivos De Neuro-Psiquiatria|December 6, 2001
Familial Creutzfeldt-Jakob disease associated with a point mutation at codon 210 of the prion protein geneN Huang, S K Marie, F Kok, et al.
Human Molecular Genetics|June 1, 1994
Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapyM R Passos-Bueno, M Vainzof, S K Marie, et al.
Neurology|August 13, 2003
14-3-3 protein in the CSF of patients with rapidly progressive dementiaN Huang, S K Marie, J A Livramento, et al.
Journal of Medical Genetics|January 1, 1995
Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian familiesM R Passos-Bueno, A Cerqueira, M Vainzof, et al.
Human Molecular Genetics|June 1, 1996
Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMDM R Passos-Bueno, E S Moreira, M Vainzof, et al.
Journal of the Neurological Sciences|March 10, 2001
Diffusion-weighted MRI in two cases of familial Creutzfeldt--Jakob diseaseR Nitrini, R A Mendonça, N Huang, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complexM Vainzof, E S Moreira, G Ferraz, et al.
Human Molecular Genetics|March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Epilepsia|May 1, 1996
Double pathology in Rasmussen's encephalitis: etiologic considerationsE M Yacubian, S Rosemberg, S K Marie, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Pediatric Neurology|July 1, 1994
Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV)S Rosemberg, S K Marie, S Kliemann
Arquivos De Neuro-Psiquiatria|December 6, 2001
Familial Creutzfeldt-Jakob disease associated with a point mutation at codon 210 of the prion protein geneN Huang, S K Marie, F Kok, et al.
Human Molecular Genetics|June 1, 1994
Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapyM R Passos-Bueno, M Vainzof, S K Marie, et al.
Neurology|August 13, 2003
14-3-3 protein in the CSF of patients with rapidly progressive dementiaN Huang, S K Marie, J A Livramento, et al.
Journal of Medical Genetics|January 1, 1995
Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian familiesM R Passos-Bueno, A Cerqueira, M Vainzof, et al.
Human Molecular Genetics|June 1, 1996
Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMDM R Passos-Bueno, E S Moreira, M Vainzof, et al.
Journal of the Neurological Sciences|March 10, 2001
Diffusion-weighted MRI in two cases of familial Creutzfeldt--Jakob diseaseR Nitrini, R A Mendonça, N Huang, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complexM Vainzof, E S Moreira, G Ferraz, et al.
Human Molecular Genetics|March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Epilepsia|May 1, 1996
Double pathology in Rasmussen's encephalitis: etiologic considerationsE M Yacubian, S Rosemberg, S K Marie, et al.
Pageof 5