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C Doriguzzi

Showing results (21-30 of 55) with videos related to

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Neurology|February 11, 2000
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same familyL Palmucci, T Mongini, L Chiadò-Piat, et al.
Neuroscience Letters|November 23, 1992
Absence of dystrophin in two patients with Becker type Xp21 muscular dystrophyT Mongini, L Palmucci, C Doriguzzi, et al.
European Neurology|January 1, 1993
Clinical spectrum of McArdle disease: three cases with unusual expressionL Chiadò-Piat, T Mongini, C Doriguzzi, et al.
European Neurology|January 1, 1989
Sporadic distal myopathy with early adult onset: study of muscle biopsies and muscle cell culturesT Mongini, C Doriguzzi, L Palmucci, et al.
British Medical Journal (Clinical Research Ed.)|March 19, 1988
Body building and myoglobinuria: report of three casesC Doriguzzi, L Palmucci, T Mongini, et al.
Prenatal Diagnosis|July 1, 1995
Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected childG Restagno, M Ferrone, C Doriguzzi, et al.
Clinical Neuropathology|May 15, 2002
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutationT Mongini, C Doriguzzi, L Chiadò-Piat, et al.
Journal of Neurology|September 1, 1991
Myoglobinuria and carnitine palmityl transferase deficiency in father and sonT Mongini, C Doriguzzi, L Palmucci, et al.
Italian Journal of Neurological Sciences|December 1, 1988
Neuropathy secondary to vitamin E deficiency in acquired intestinal malabsorptionL Palmucci, C Doriguzzi, L Orsi, et al.
Journal of Neurology|May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Neurology|February 11, 2000
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same familyL Palmucci, T Mongini, L Chiadò-Piat, et al.
Neuroscience Letters|November 23, 1992
Absence of dystrophin in two patients with Becker type Xp21 muscular dystrophyT Mongini, L Palmucci, C Doriguzzi, et al.
European Neurology|January 1, 1993
Clinical spectrum of McArdle disease: three cases with unusual expressionL Chiadò-Piat, T Mongini, C Doriguzzi, et al.
European Neurology|January 1, 1989
Sporadic distal myopathy with early adult onset: study of muscle biopsies and muscle cell culturesT Mongini, C Doriguzzi, L Palmucci, et al.
British Medical Journal (Clinical Research Ed.)|March 19, 1988
Body building and myoglobinuria: report of three casesC Doriguzzi, L Palmucci, T Mongini, et al.
Prenatal Diagnosis|July 1, 1995
Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected childG Restagno, M Ferrone, C Doriguzzi, et al.
Clinical Neuropathology|May 15, 2002
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutationT Mongini, C Doriguzzi, L Chiadò-Piat, et al.
Journal of Neurology|September 1, 1991
Myoglobinuria and carnitine palmityl transferase deficiency in father and sonT Mongini, C Doriguzzi, L Palmucci, et al.
Italian Journal of Neurological Sciences|December 1, 1988
Neuropathy secondary to vitamin E deficiency in acquired intestinal malabsorptionL Palmucci, C Doriguzzi, L Orsi, et al.
Journal of Neurology|May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
Pageof 6