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N Bresolin

Showing results (61-70 of 206) with videos related to

Pageof 21
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Lancet (London, England)|July 30, 1994
Rapid direct diagnosis of deletions carriers of Duchenne and Becker muscular dystrophiesA Fassati, S Tedeschi, A Bordoni, et al.
Muscle & Nerve|June 1, 1994
Immunocytochemistry of muscle cytoskeletal proteins in acid maltase deficiencyG Vita, A Migliorato, A Toscano, et al.
Biochemical Society Transactions|August 1, 1985
Cytochrome c oxidase deficiencyS DiMauro, M Zeviani, E Bonilla, et al.
FEBS Letters|June 14, 2002
The dystrophin gene is alternatively spliced throughout its coding sequenceM Sironi, R Cagliani, U Pozzoli, et al.
Neurology|July 1, 1981
Carnitine palmityl transferase deficiency: clinical variability, carrier detection, and autosomal-recessive inheritanceC Angelini, L Freddo, P Battistella, et al.
FEBS Letters|February 28, 2003
Trans-acting factors may cause dystrophin splicing misregulation in BMD skeletal musclesM Sironi, R Cagliani, G P Comi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 3, 2011
The genetic features of 24 patients affected by familial and sporadic hemiplegic migraineA Gallanti, V Cardin, A Tonelli, et al.
Life Sciences|May 4, 2000
Iron release and oxidant damage in human myoblasts by divicineP Ninfali, M P Perini, N Bresolin, et al.
Annals of Neurology|February 24, 2001
Down's syndrome fibroblasts anticipate the accumulation of specific ageing-related mtDNA mutationsR Del Bo, G P Comi, M P Perini, et al.
Electromyography and Clinical Neurophysiology|August 9, 2005
Early peripheral nerve abnormalities in impaired glucose toleranceA Cappellari, L Airaghi, R Capra, et al.
Pageof 21

Showing results (61-70 of 206) with videos related to

Sort By:
Pageof 21
Lancet (London, England)|July 30, 1994
Rapid direct diagnosis of deletions carriers of Duchenne and Becker muscular dystrophiesA Fassati, S Tedeschi, A Bordoni, et al.
Muscle & Nerve|June 1, 1994
Immunocytochemistry of muscle cytoskeletal proteins in acid maltase deficiencyG Vita, A Migliorato, A Toscano, et al.
Biochemical Society Transactions|August 1, 1985
Cytochrome c oxidase deficiencyS DiMauro, M Zeviani, E Bonilla, et al.
FEBS Letters|June 14, 2002
The dystrophin gene is alternatively spliced throughout its coding sequenceM Sironi, R Cagliani, U Pozzoli, et al.
Neurology|July 1, 1981
Carnitine palmityl transferase deficiency: clinical variability, carrier detection, and autosomal-recessive inheritanceC Angelini, L Freddo, P Battistella, et al.
FEBS Letters|February 28, 2003
Trans-acting factors may cause dystrophin splicing misregulation in BMD skeletal musclesM Sironi, R Cagliani, G P Comi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 3, 2011
The genetic features of 24 patients affected by familial and sporadic hemiplegic migraineA Gallanti, V Cardin, A Tonelli, et al.
Life Sciences|May 4, 2000
Iron release and oxidant damage in human myoblasts by divicineP Ninfali, M P Perini, N Bresolin, et al.
Annals of Neurology|February 24, 2001
Down's syndrome fibroblasts anticipate the accumulation of specific ageing-related mtDNA mutationsR Del Bo, G P Comi, M P Perini, et al.
Electromyography and Clinical Neurophysiology|August 9, 2005
Early peripheral nerve abnormalities in impaired glucose toleranceA Cappellari, L Airaghi, R Capra, et al.
Pageof 21