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C Minetti

Showing results (51-60 of 114) with videos related to

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Neurology|December 15, 2004
Middle interhemispheric variant of holoprosencephaly: a very mild clinical caseR Biancheri, A Rossi, P Tortori-Donati, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 6, 2007
Neuromuscular forms of glycogen branching enzyme deficiencyC Bruno, D Cassandrini, S Assereto, et al.
Minerva Pediatrica|March 1, 1991
[Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene]E Bonilla, C Minetti, H W Chang, et al.
Skeletal Muscle|July 28, 2016
ActRII blockade protects mice from cancer cachexia and prolongs survival in the presence of anti-cancer treatmentsShinji Hatakeyama, Serge Summermatter, Marie Jourdain, et al.
Neuropediatrics|November 1, 1982
Familial nemaline myopathyG Scarlato, G Pellegrini, M Moggio, et al.
Neurology|January 27, 1998
Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuriaC Bruno, C Minetti, S Shanske, et al.
Minerva Pediatrica|November 30, 1983
[Ophthalmoplegia plus and ragged red fibers. Description of a case manifested in childhood]E De Langlade, G Corazza, C Minetti, et al.
Minerva Pediatrica|March 1, 1991
[The defect in muscular glucose-6-phosphate dehydrogenase]M Bado, C Minetti, L Mallamaci, et al.
Clinical Genetics|July 14, 2016
WES in a family trio suggests involvement of TECPR2 in a complex form of progressive motor neuron diseaseA E Covone, C Fiorillo, M Acquaviva, et al.
Muscle & Nerve|January 1, 1996
Ubiquitin expression in acute steroid myopathy with loss of myosin thick filamentsC Minetti, M Hirano, G Morreale, et al.
Pageof 12

Showing results (51-60 of 114) with videos related to

Sort By:
Pageof 12
Neurology|December 15, 2004
Middle interhemispheric variant of holoprosencephaly: a very mild clinical caseR Biancheri, A Rossi, P Tortori-Donati, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 6, 2007
Neuromuscular forms of glycogen branching enzyme deficiencyC Bruno, D Cassandrini, S Assereto, et al.
Minerva Pediatrica|March 1, 1991
[Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene]E Bonilla, C Minetti, H W Chang, et al.
Skeletal Muscle|July 28, 2016
ActRII blockade protects mice from cancer cachexia and prolongs survival in the presence of anti-cancer treatmentsShinji Hatakeyama, Serge Summermatter, Marie Jourdain, et al.
Neuropediatrics|November 1, 1982
Familial nemaline myopathyG Scarlato, G Pellegrini, M Moggio, et al.
Neurology|January 27, 1998
Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuriaC Bruno, C Minetti, S Shanske, et al.
Minerva Pediatrica|November 30, 1983
[Ophthalmoplegia plus and ragged red fibers. Description of a case manifested in childhood]E De Langlade, G Corazza, C Minetti, et al.
Minerva Pediatrica|March 1, 1991
[The defect in muscular glucose-6-phosphate dehydrogenase]M Bado, C Minetti, L Mallamaci, et al.
Clinical Genetics|July 14, 2016
WES in a family trio suggests involvement of TECPR2 in a complex form of progressive motor neuron diseaseA E Covone, C Fiorillo, M Acquaviva, et al.
Muscle & Nerve|January 1, 1996
Ubiquitin expression in acute steroid myopathy with loss of myosin thick filamentsC Minetti, M Hirano, G Morreale, et al.
Pageof 12