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Neurology|May 1, 1996
Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiencyC Minetti, M Bado, G Morreale, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 1, 1996
Severe dystrophinopathy in a patient with congenital hypotoniaG Cordone, M Bado, G Morreale, et al.Muscle & Nerve|February 18, 1998
Disorganization of dystrophin costameric lattice in Becker muscular dystrophyC Minetti, G Cordone, F Beltrame, et al.Journal of Child Neurology|June 27, 2000
Novel mutation in the CPT II gene in a child with periodic febrile myalgia and myoglobinuriaC Bruno, M Bado, C Minetti, et al.Minerva Pediatrica|June 1, 1995
[Early myoclonic encephalopathy and spinal muscular atrophy type I]M Bado, C Bruno, G Morreale, 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|October 1, 1994
[Muscle phosphorylase deficiency in childhood. A case report]C Bruno, A Iester, M Bado, 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.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1984
[Critical evaluation of changes of serum CK after exertion in the identification of carriers of Duchenne's muscular dystrophy]G Cordone, V Venzano, G Rossi, et al.Pageof 11