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M Bado

Showing results (21-30 of 31) with videos related to

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European Journal of Pediatrics|November 1, 1996
Diagnostic problems in congenital myotonic dystrophyM DiRocco, M Gennarelli, E Veneselli, et al.
Clinical Genetics|July 18, 2002
Tubulopathy, endocrinopathies and encephalomyopathy in a child with a novel large-scale mitochondrial DNA deletionC Bruno, P Gandullia, F M Santorelli, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuriaC Minetti, B Garavaglia, M Bado, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletionC Bruno, C Minetti, Y Tang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2004
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effectE Di Maria, R Gulli, P Balestra, et al.
Annals of Neurology|May 13, 1999
Congenital hypomyelination due to myelin protein zero Q215X mutationP Mandich, G L Mancardi, A Varese, et al.
Biochemical and Biophysical Research Communications|August 12, 1999
Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophyS Repetto, M Bado, P Broda, et al.
Neuromuscular Disorders : NMD|November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathyC Bruno, M DiRocco, L D Lamba, et al.
Neurology|April 4, 2000
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemiaI Carbone, C Bruno, F Sotgia, et al.
Nature Genetics|April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophyC Minetti, F Sotgia, C Bruno, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
European Journal of Pediatrics|November 1, 1996
Diagnostic problems in congenital myotonic dystrophyM DiRocco, M Gennarelli, E Veneselli, et al.
Clinical Genetics|July 18, 2002
Tubulopathy, endocrinopathies and encephalomyopathy in a child with a novel large-scale mitochondrial DNA deletionC Bruno, P Gandullia, F M Santorelli, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuriaC Minetti, B Garavaglia, M Bado, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletionC Bruno, C Minetti, Y Tang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2004
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effectE Di Maria, R Gulli, P Balestra, et al.
Annals of Neurology|May 13, 1999
Congenital hypomyelination due to myelin protein zero Q215X mutationP Mandich, G L Mancardi, A Varese, et al.
Biochemical and Biophysical Research Communications|August 12, 1999
Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophyS Repetto, M Bado, P Broda, et al.
Neuromuscular Disorders : NMD|November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathyC Bruno, M DiRocco, L D Lamba, et al.
Neurology|April 4, 2000
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemiaI Carbone, C Bruno, F Sotgia, et al.
Nature Genetics|April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophyC Minetti, F Sotgia, C Bruno, et al.
Pageof 4