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S Servidei

Showing results (91-100 of 146) with videos related to

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Journal of Clinical Gastroenterology|July 29, 2000
Hepatocellular carcinoma complicating liver cirrhosis in type IIIa glycogen storage diseaseM Siciliano, E De Candia, S Ballarin, et al.
Neurology|April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiencyG Silvestri, T Mongini, F Odoardi, et al.
Neurology|June 1, 1993
Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation")G Silvestri, E Ciafaloni, F M Santorelli, et al.
FEBS Letters|December 31, 1997
Mitochondrial DNA deletions in oculopharyngeal muscular dystrophyA M Lezza, A Cormio, P Gerardi, et al.
Neurology|November 1, 1986
Fatal infantile form of muscle phosphofructokinase deficiencyS Servidei, E Bonilla, R G Diedrich, et al.
Journal of the Neurological Sciences|March 1, 1993
Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a familyG Manfredi, G Silvestri, S Servidei, et al.
Human Gene Therapy|December 1, 1993
Retroviral vector-mediated gene transfer into human primary myogenic cells leads to expression in muscle fibers in vivoG Salvatori, G Ferrari, A Mezzogiorno, et al.
Human Molecular Genetics|May 20, 1999
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expressionZ Korade-Mirnics, J Tarleton, S Servidei, et al.
Acta Neuropathologica|January 1, 1994
Autosomal recessive hypermyelinating neuropathyM Sabatelli, T Mignogna, G Lippi, et al.
Journal of the Neurological Sciences|April 1, 1995
Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraineA Uncini, R Lodi, A Di Muzio, et al.
Pageof 15

Showing results (91-100 of 146) with videos related to

Sort By:
Pageof 15
Journal of Clinical Gastroenterology|July 29, 2000
Hepatocellular carcinoma complicating liver cirrhosis in type IIIa glycogen storage diseaseM Siciliano, E De Candia, S Ballarin, et al.
Neurology|April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiencyG Silvestri, T Mongini, F Odoardi, et al.
Neurology|June 1, 1993
Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation")G Silvestri, E Ciafaloni, F M Santorelli, et al.
FEBS Letters|December 31, 1997
Mitochondrial DNA deletions in oculopharyngeal muscular dystrophyA M Lezza, A Cormio, P Gerardi, et al.
Neurology|November 1, 1986
Fatal infantile form of muscle phosphofructokinase deficiencyS Servidei, E Bonilla, R G Diedrich, et al.
Journal of the Neurological Sciences|March 1, 1993
Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a familyG Manfredi, G Silvestri, S Servidei, et al.
Human Gene Therapy|December 1, 1993
Retroviral vector-mediated gene transfer into human primary myogenic cells leads to expression in muscle fibers in vivoG Salvatori, G Ferrari, A Mezzogiorno, et al.
Human Molecular Genetics|May 20, 1999
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expressionZ Korade-Mirnics, J Tarleton, S Servidei, et al.
Acta Neuropathologica|January 1, 1994
Autosomal recessive hypermyelinating neuropathyM Sabatelli, T Mignogna, G Lippi, et al.
Journal of the Neurological Sciences|April 1, 1995
Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraineA Uncini, R Lodi, A Di Muzio, et al.
Pageof 15