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C Minetti

Showing results (61-70 of 114) with videos related to

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Minerva Pediatrica|October 1, 1991
[Infantile dermatomyositis. Clinical aspects and prospective treatments]G Cordone, A Buoncompagni, O Ciccone, et al.
European Journal of Pediatrics|October 1, 1993
Dystrophinopathy in two young boys with exercise-induced cramps and myoglobinuriaC Minetti, K Tanji, H W Chang, et al.
Neurology|August 1, 1991
Dystrophin deficiency in young girls with sporadic myopathy and normal karyotypeC Minetti, H W Chang, R Medori, et al.
Minerva Pediatrica|October 1, 1994
[Muscle phosphorylase deficiency in childhood. A case report]C Bruno, A Iester, M Bado, et al.
Transboundary and Emerging Diseases|March 12, 2013
Occurrence and diversity of Giardia duodenalis assemblages in livestock in the UKC Minetti, W Taweenan, R Hogg, et al.
Diabetologia|February 15, 2002
A novel hepatocyte nuclear factor-1beta (MODY-5) gene mutation in an Italian family with renal dysfunctions and early-onset diabetesI Carbone, M Cotellessa, C Barella, 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.
Arquivos De Neuro-Psiquiatria|December 1, 1992
Carrier detection of Duchenne and Becker muscular dystrophy using muscle dystrophin immunohistochemistryA S Oliveira, A A Gabbai, B Schmidt, 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 Neurology, Neurosurgery, and Psychiatry|June 26, 2002
Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) geneL Merlini, I Carbone, C Capanni, et al.
Pageof 12

Showing results (61-70 of 114) with videos related to

Sort By:
Pageof 12
Minerva Pediatrica|October 1, 1991
[Infantile dermatomyositis. Clinical aspects and prospective treatments]G Cordone, A Buoncompagni, O Ciccone, et al.
European Journal of Pediatrics|October 1, 1993
Dystrophinopathy in two young boys with exercise-induced cramps and myoglobinuriaC Minetti, K Tanji, H W Chang, et al.
Neurology|August 1, 1991
Dystrophin deficiency in young girls with sporadic myopathy and normal karyotypeC Minetti, H W Chang, R Medori, et al.
Minerva Pediatrica|October 1, 1994
[Muscle phosphorylase deficiency in childhood. A case report]C Bruno, A Iester, M Bado, et al.
Transboundary and Emerging Diseases|March 12, 2013
Occurrence and diversity of Giardia duodenalis assemblages in livestock in the UKC Minetti, W Taweenan, R Hogg, et al.
Diabetologia|February 15, 2002
A novel hepatocyte nuclear factor-1beta (MODY-5) gene mutation in an Italian family with renal dysfunctions and early-onset diabetesI Carbone, M Cotellessa, C Barella, 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.
Arquivos De Neuro-Psiquiatria|December 1, 1992
Carrier detection of Duchenne and Becker muscular dystrophy using muscle dystrophin immunohistochemistryA S Oliveira, A A Gabbai, B Schmidt, 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 Neurology, Neurosurgery, and Psychiatry|June 26, 2002
Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) geneL Merlini, I Carbone, C Capanni, et al.
Pageof 12