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S Servidei

Showing results (111-120 of 146) with videos related to

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American Journal of Medical Genetics|March 31, 1997
Asymptomatic dystrophinopathyA Morrone, E Zammarchi, P C Scacheri, et al.
Neurology|August 15, 2001
Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiencyS Di Giovanni, M Mirabella, A Spinazzola, et al.
Cephalalgia : an International Journal of Headache|May 25, 2005
Hypnic headache: actigraphic and polysomnographic study of a caseA Capuano, C Vollono, M Rubino, et al.
Annals of Neurology|January 1, 1993
Glycogen branching enzyme deficiency in adult polyglucosan body diseaseC Bruno, S Servidei, S Shanske, et al.
The Journal of Pediatrics|July 1, 1987
Severe cardiopathy in branching enzyme deficiencyS Servidei, R E Riepe, C Langston, et al.
The Journal of Biological Chemistry|April 5, 2000
Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cellsG Piluso, M Mirabella, E Ricci, et al.
Human Genetics|October 1, 1994
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)S Cacurri, G Deidda, N Piazzo, et al.
Acta Neuropathologica|January 1, 1987
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorderA Bardosi, W Creutzfeldt, S DiMauro, et al.
Neurology|July 1, 1991
Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studiesS Servidei, M Zeviani, G Manfredi, et al.
Muscle & Nerve|June 1, 1994
Ophthalmoplegia, demyelinating neuropathy, leukoencephalopathy, myopathy, and gastrointestinal dysfunction with multiple deletions of mitochondrial DNA: a mitochondrial multisystem disorder in search of a nameA Uncini, S Servidei, G Silvestri, et al.
Pageof 15

Showing results (111-120 of 146) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics|March 31, 1997
Asymptomatic dystrophinopathyA Morrone, E Zammarchi, P C Scacheri, et al.
Neurology|August 15, 2001
Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiencyS Di Giovanni, M Mirabella, A Spinazzola, et al.
Cephalalgia : an International Journal of Headache|May 25, 2005
Hypnic headache: actigraphic and polysomnographic study of a caseA Capuano, C Vollono, M Rubino, et al.
Annals of Neurology|January 1, 1993
Glycogen branching enzyme deficiency in adult polyglucosan body diseaseC Bruno, S Servidei, S Shanske, et al.
The Journal of Pediatrics|July 1, 1987
Severe cardiopathy in branching enzyme deficiencyS Servidei, R E Riepe, C Langston, et al.
The Journal of Biological Chemistry|April 5, 2000
Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cellsG Piluso, M Mirabella, E Ricci, et al.
Human Genetics|October 1, 1994
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)S Cacurri, G Deidda, N Piazzo, et al.
Acta Neuropathologica|January 1, 1987
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorderA Bardosi, W Creutzfeldt, S DiMauro, et al.
Neurology|July 1, 1991
Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studiesS Servidei, M Zeviani, G Manfredi, et al.
Muscle & Nerve|June 1, 1994
Ophthalmoplegia, demyelinating neuropathy, leukoencephalopathy, myopathy, and gastrointestinal dysfunction with multiple deletions of mitochondrial DNA: a mitochondrial multisystem disorder in search of a nameA Uncini, S Servidei, G Silvestri, et al.
Pageof 15