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S Servidei

Showing results (71-80 of 146) with videos related to

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Neurology|November 1, 1993
Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophyM Mirabella, S Servidei, G Manfredi, et al.
American Journal of Medical Genetics|December 1, 1986
Metabolic myopathiesS DiMauro, A F Miranda, S Sakoda, et al.
Human Mutation|April 24, 1999
Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. OnlineF Sangiuolo, A Botta, A Mesoraca, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 12, 2007
Acute necrotizing encephalopathy: a relapsing case in a European adultA Fasano, G F Natoli, A Cianfoni, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Cytochrome oxidase deficiency: clinical and biochemical heterogeneityS DiMauro, M Zeviani, S Servidei, et al.
Muscle & Nerve|February 1, 1991
Polyglucosan body diseaseM S Cafferty, R E Lovelace, A P Hays, et al.
Advances in Neurology|January 1, 1988
Biochemical and molecular aspects of cytochrome C oxidase deficiencyS DiMauro, M Zeviani, S Servidei, et al.
Acta Neuropathologica|January 1, 1994
Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findingsE Bertini, G Salviati, F Apollo, et al.
Experimental and Molecular Pathology|July 20, 1999
Molecular characterization of a novel endonuclease (Xib) and possible involvement in lysosomal glycogen storage disordersG Malferrari, U Mazza, C Tresoldi, et al.
Neurology|April 1, 1995
High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathyG Manfredi, S Servidei, E Bonilla, et al.
Pageof 15

Showing results (71-80 of 146) with videos related to

Sort By:
Pageof 15
Neurology|November 1, 1993
Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophyM Mirabella, S Servidei, G Manfredi, et al.
American Journal of Medical Genetics|December 1, 1986
Metabolic myopathiesS DiMauro, A F Miranda, S Sakoda, et al.
Human Mutation|April 24, 1999
Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. OnlineF Sangiuolo, A Botta, A Mesoraca, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 12, 2007
Acute necrotizing encephalopathy: a relapsing case in a European adultA Fasano, G F Natoli, A Cianfoni, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Cytochrome oxidase deficiency: clinical and biochemical heterogeneityS DiMauro, M Zeviani, S Servidei, et al.
Muscle & Nerve|February 1, 1991
Polyglucosan body diseaseM S Cafferty, R E Lovelace, A P Hays, et al.
Advances in Neurology|January 1, 1988
Biochemical and molecular aspects of cytochrome C oxidase deficiencyS DiMauro, M Zeviani, S Servidei, et al.
Acta Neuropathologica|January 1, 1994
Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findingsE Bertini, G Salviati, F Apollo, et al.
Experimental and Molecular Pathology|July 20, 1999
Molecular characterization of a novel endonuclease (Xib) and possible involvement in lysosomal glycogen storage disordersG Malferrari, U Mazza, C Tresoldi, et al.
Neurology|April 1, 1995
High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathyG Manfredi, S Servidei, E Bonilla, et al.
Pageof 15