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T Mongini

Showing results (31-40 of 83) with videos related to

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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.
Neurology|March 1, 1994
Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion of the dystrophin geneL Palmucci, C Doriguzzi, T Mongini, et al.
Clinical Neuropathology|July 1, 1985
Spongiform encephalopathy in addicts inhaling pre-heated heroinD Schiffer, F Brignolio, M T Giordana, 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.
Advances in Experimental Medicine and Biology|January 1, 1990
Myogenic conversion of human non-muscle cells for the diagnosis and therapy of neuromuscular diseasesA F Miranda, T Mongini, E Bonilla, 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.
Minerva Medica|September 15, 1980
[Progressive muscular dystrophy of the Duchenne type. Epidemiology and strategy for prevention]C Doriguzzi, A Bertolotto, T Mongini, et al.
Neuropediatrics|June 21, 2001
Myopathy in a patient with chromosome 22q11 deletionT Mongini, C Doriguzzi, C Arduino, et al.
Journal of the Neurological Sciences|February 1, 1986
Quantitative analysis of quadriceps muscle biopsy. Results in 7 definite and 45 possible carriers of Duchenne muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
Social Psychiatry and Psychiatric Epidemiology|July 9, 2009
Outcome and length of stay in psychiatric hospitalization, the experience of the University Clinic of TurinPaola Rocca, C Mingrone, T Mongini, et al.
Pageof 9

Showing results (31-40 of 83) with videos related to

Sort By:
Pageof 9
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.
Neurology|March 1, 1994
Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion of the dystrophin geneL Palmucci, C Doriguzzi, T Mongini, et al.
Clinical Neuropathology|July 1, 1985
Spongiform encephalopathy in addicts inhaling pre-heated heroinD Schiffer, F Brignolio, M T Giordana, 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.
Advances in Experimental Medicine and Biology|January 1, 1990
Myogenic conversion of human non-muscle cells for the diagnosis and therapy of neuromuscular diseasesA F Miranda, T Mongini, E Bonilla, 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.
Minerva Medica|September 15, 1980
[Progressive muscular dystrophy of the Duchenne type. Epidemiology and strategy for prevention]C Doriguzzi, A Bertolotto, T Mongini, et al.
Neuropediatrics|June 21, 2001
Myopathy in a patient with chromosome 22q11 deletionT Mongini, C Doriguzzi, C Arduino, et al.
Journal of the Neurological Sciences|February 1, 1986
Quantitative analysis of quadriceps muscle biopsy. Results in 7 definite and 45 possible carriers of Duchenne muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
Social Psychiatry and Psychiatric Epidemiology|July 9, 2009
Outcome and length of stay in psychiatric hospitalization, the experience of the University Clinic of TurinPaola Rocca, C Mingrone, T Mongini, et al.
Pageof 9