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C Doriguzzi

Showing results (41-50 of 55) with videos related to

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Journal of the Neurological Sciences|September 1, 1992
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophyL Palmucci, C Doriguzzi, T Mongini, et al.
Journal of the Neurological Sciences|August 1, 1983
Laminin and fibronectin distribution in normal and pathological human muscleA Bertolotto, L Palmucci, C Doriguzzi, et al.
Neurogenetics|March 25, 2000
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory diseaseA Migheli, T Mongini, C Doriguzzi, et al.
Neurology|March 1, 1988
Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patientsT Mongini, D Ghigo, C Doriguzzi, et al.
Revue Neurologique|January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathiesG Scarlato, N Bresolin, I Moroni, et al.
Minerva Pediatrica|August 31, 1986
[Individualization of carriers of Duchenne's muscular dystrophy by quantitative methods]C Doriguzzi, L Palmucci, T Mongini, et al.
Acta Neuropathologica|June 23, 1999
Variable histological expression of dystrophinopathy in two femalesC Doriguzzi, L Palmucci, T Mongini, 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.
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.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Journal of the Neurological Sciences|September 1, 1992
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophyL Palmucci, C Doriguzzi, T Mongini, et al.
Journal of the Neurological Sciences|August 1, 1983
Laminin and fibronectin distribution in normal and pathological human muscleA Bertolotto, L Palmucci, C Doriguzzi, et al.
Neurogenetics|March 25, 2000
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory diseaseA Migheli, T Mongini, C Doriguzzi, et al.
Neurology|March 1, 1988
Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patientsT Mongini, D Ghigo, C Doriguzzi, et al.
Revue Neurologique|January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathiesG Scarlato, N Bresolin, I Moroni, et al.
Minerva Pediatrica|August 31, 1986
[Individualization of carriers of Duchenne's muscular dystrophy by quantitative methods]C Doriguzzi, L Palmucci, T Mongini, et al.
Acta Neuropathologica|June 23, 1999
Variable histological expression of dystrophinopathy in two femalesC Doriguzzi, L Palmucci, T Mongini, 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.
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.
Pageof 6