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S Servidei

Showing results (51-60 of 146) with videos related to

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Pathologica|January 1, 1988
[Viral hepatitis B and polymyositis. Description of a case of polymyositis associated with viral hepatitis B]E Pizzigallo, R Cauda, F Pallavicini, et al.
Clinical and Experimental Immunology|January 1, 1994
MHC class I, MHC class II and intercellular adhesion molecule-1 (ICAM-1) expression in inflammatory myopathiesE Bartoccioni, S Gallucci, F Scuderi, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Mitochondrial myopathiesS DiMauro, E Bonilla, M Zeviani, et al.
Muscle & Nerve|February 1, 1997
Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation)G Silvestri, E Bertini, S Servidei, et al.
Neurology|January 1, 1987
Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiencyS Servidei, R P Lazaro, E Bonilla, et al.
American Journal of Medical Genetics|February 1, 1993
Presymptomatic diagnosis of SMA III by genotype analysisC Brahe, S Zappata, I Velonà, et al.
Biochemical and Biophysical Research Communications|March 27, 1996
A novel mitochondrial DNA point mutation in the tRNA(Ile) gene is associated with progressive external ophtalmoplegiaG Silvestri, S Servidei, M Rana, et al.
Annals of Neurology|July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathiesM Zeviani, C Gellera, M Pannacci, et al.
Neurology|February 1, 1995
Myasthenia gravis during interferon alfa therapyA P Batocchi, A Evoli, S Servidei, et al.
Acta Neuropathologica|January 1, 1991
Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical studyE Bertini, C Bosman, E Ricci, et al.
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
Pathologica|January 1, 1988
[Viral hepatitis B and polymyositis. Description of a case of polymyositis associated with viral hepatitis B]E Pizzigallo, R Cauda, F Pallavicini, et al.
Clinical and Experimental Immunology|January 1, 1994
MHC class I, MHC class II and intercellular adhesion molecule-1 (ICAM-1) expression in inflammatory myopathiesE Bartoccioni, S Gallucci, F Scuderi, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Mitochondrial myopathiesS DiMauro, E Bonilla, M Zeviani, et al.
Muscle & Nerve|February 1, 1997
Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation)G Silvestri, E Bertini, S Servidei, et al.
Neurology|January 1, 1987
Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiencyS Servidei, R P Lazaro, E Bonilla, et al.
American Journal of Medical Genetics|February 1, 1993
Presymptomatic diagnosis of SMA III by genotype analysisC Brahe, S Zappata, I Velonà, et al.
Biochemical and Biophysical Research Communications|March 27, 1996
A novel mitochondrial DNA point mutation in the tRNA(Ile) gene is associated with progressive external ophtalmoplegiaG Silvestri, S Servidei, M Rana, et al.
Annals of Neurology|July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathiesM Zeviani, C Gellera, M Pannacci, et al.
Neurology|February 1, 1995
Myasthenia gravis during interferon alfa therapyA P Batocchi, A Evoli, S Servidei, et al.
Acta Neuropathologica|January 1, 1991
Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical studyE Bertini, C Bosman, E Ricci, et al.
Pageof 15