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Journal of Neurology
|
May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy
C 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 gene
L Palmucci, C Doriguzzi, T Mongini, et al.
Clinical Neuropathology
|
July 1, 1985
Spongiform encephalopathy in addicts inhaling pre-heated heroin
D Schiffer, F Brignolio, M T Giordana, et al.
Clinical Neuropathology
|
May 15, 2002
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation
T 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 diseases
A F Miranda, T Mongini, E Bonilla, et al.
Journal of Neurology
|
September 1, 1991
Myoglobinuria and carnitine palmityl transferase deficiency in father and son
T 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 deletion
T 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 dystrophy
C 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 Turin
Paola Rocca, C Mingrone, T Mongini, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 83) with videos related to
Sort By:
Page
of 9
Journal of Neurology
|
May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy
C 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 gene
L Palmucci, C Doriguzzi, T Mongini, et al.
Clinical Neuropathology
|
July 1, 1985
Spongiform encephalopathy in addicts inhaling pre-heated heroin
D Schiffer, F Brignolio, M T Giordana, et al.
Clinical Neuropathology
|
May 15, 2002
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation
T 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 diseases
A F Miranda, T Mongini, E Bonilla, et al.
Journal of Neurology
|
September 1, 1991
Myoglobinuria and carnitine palmityl transferase deficiency in father and son
T 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 deletion
T 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 dystrophy
C 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 Turin
Paola Rocca, C Mingrone, T Mongini, et al.
Page
of 9