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T Mongini

Showing results (51-60 of 83) with videos related to

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Italian Journal of Neurological Sciences|January 1, 1981
Epidemiology of Duchenne muscular dystrophy in the province of TurinA Bertolotto, M De Marchi, C Doriguzzi, et al.
European Neurology|January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult caseT Mongini, C Doriguzzi, L Palmucci, et al.
Clinical Neuropathology|October 12, 2001
Late onset and very mild course of Xp21 Becker type muscular dystrophyI Bosone, S Bortolotto, T Mongini, et al.
European Journal of Neurology|February 28, 2014
Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutationA Romagnolo, S Masera, A Mattioda, et al.
Neurology|April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiencyG Silvestri, T Mongini, F Odoardi, et al.
European Neurology|January 1, 1993
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalisC Doriguzzi, L Palmucci, T Mongini, et al.
The New England Journal of Medicine|September 23, 1993
Analysis of dystrophin expression after activation of myogenesis in amniocytes, chorionic-villus cells, and fibroblasts. A new method for diagnosing Duchenne's muscular dystrophyS Sancho, T Mongini, K Tanji, et al.
Human Mutation|August 3, 2000
A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) geneD Pirulli, S Zezlina, L Vatta, et al.
Neuromuscular Disorders : NMD|May 1, 1996
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiencyM Villanova, A Malandrini, R Biancotti, et al.
European Journal of Neurology|May 1, 2013
EFNS review on the role of muscle biopsy in the investigation of myalgiaT Kyriakides, C Angelini, J Schaefer, et al.
Pageof 9

Showing results (51-60 of 83) with videos related to

Sort By:
Pageof 9
Italian Journal of Neurological Sciences|January 1, 1981
Epidemiology of Duchenne muscular dystrophy in the province of TurinA Bertolotto, M De Marchi, C Doriguzzi, et al.
European Neurology|January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult caseT Mongini, C Doriguzzi, L Palmucci, et al.
Clinical Neuropathology|October 12, 2001
Late onset and very mild course of Xp21 Becker type muscular dystrophyI Bosone, S Bortolotto, T Mongini, et al.
European Journal of Neurology|February 28, 2014
Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutationA Romagnolo, S Masera, A Mattioda, et al.
Neurology|April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiencyG Silvestri, T Mongini, F Odoardi, et al.
European Neurology|January 1, 1993
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalisC Doriguzzi, L Palmucci, T Mongini, et al.
The New England Journal of Medicine|September 23, 1993
Analysis of dystrophin expression after activation of myogenesis in amniocytes, chorionic-villus cells, and fibroblasts. A new method for diagnosing Duchenne's muscular dystrophyS Sancho, T Mongini, K Tanji, et al.
Human Mutation|August 3, 2000
A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) geneD Pirulli, S Zezlina, L Vatta, et al.
Neuromuscular Disorders : NMD|May 1, 1996
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiencyM Villanova, A Malandrini, R Biancotti, et al.
European Journal of Neurology|May 1, 2013
EFNS review on the role of muscle biopsy in the investigation of myalgiaT Kyriakides, C Angelini, J Schaefer, et al.
Pageof 9