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C Angelini

Showing results (171-180 of 531) with videos related to

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Journal of Neurology|January 1, 1981
Peroneal muscular atrophy with ataxia and partial myoclonic epilepsyC Angelini, G F Micaglio, M Armani, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 19, 2006
The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophyD M Bonifati, S F Witchel, M Ermani, et al.
Annals of Human Genetics|March 16, 2007
Association between human polymorphic DNA markers and hypoxia adaptation in Sherpa detected by a preliminary genome scanS Malacrida, Y Katsuyama, Y Droma, et al.
Muscle & Nerve|May 19, 1998
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patientC Angelini, M Fanin, E Menegazzo, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophyP Melacini, A Vianello, C Villanova, et al.
Acta Cardiologica|January 1, 1991
Echocardiographic and pulsed Doppler features in glycogen storage disease type II of the heart (Pompe's disease)E De Dominicis, G Finocchi, M Vincenzi, et al.
Neurology|August 1, 1989
Improved diagnosis of Becker muscular dystrophy by dystrophin testingE P Hoffman, L M Kunkel, C Angelini, et al.
Clinical Cardiology|April 1, 1988
The natural history of cardiac involvement in myotonic dystrophy: an eight-year follow-up in 17 patientsP Melacini, G Buja, G Fasoli, et al.
Neurology|January 1, 1987
Friedreich's disease: V. Variant form with vitamin E deficiency and normal fat absorptionD A Stumpf, R Sokol, D Bettis, et al.
Neurology|July 1, 1981
Carnitine palmityl transferase deficiency: clinical variability, carrier detection, and autosomal-recessive inheritanceC Angelini, L Freddo, P Battistella, et al.
Pageof 54

Showing results (171-180 of 531) with videos related to

Sort By:
Pageof 54
Journal of Neurology|January 1, 1981
Peroneal muscular atrophy with ataxia and partial myoclonic epilepsyC Angelini, G F Micaglio, M Armani, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 19, 2006
The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophyD M Bonifati, S F Witchel, M Ermani, et al.
Annals of Human Genetics|March 16, 2007
Association between human polymorphic DNA markers and hypoxia adaptation in Sherpa detected by a preliminary genome scanS Malacrida, Y Katsuyama, Y Droma, et al.
Muscle & Nerve|May 19, 1998
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patientC Angelini, M Fanin, E Menegazzo, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophyP Melacini, A Vianello, C Villanova, et al.
Acta Cardiologica|January 1, 1991
Echocardiographic and pulsed Doppler features in glycogen storage disease type II of the heart (Pompe's disease)E De Dominicis, G Finocchi, M Vincenzi, et al.
Neurology|August 1, 1989
Improved diagnosis of Becker muscular dystrophy by dystrophin testingE P Hoffman, L M Kunkel, C Angelini, et al.
Clinical Cardiology|April 1, 1988
The natural history of cardiac involvement in myotonic dystrophy: an eight-year follow-up in 17 patientsP Melacini, G Buja, G Fasoli, et al.
Neurology|January 1, 1987
Friedreich's disease: V. Variant form with vitamin E deficiency and normal fat absorptionD A Stumpf, R Sokol, D Bettis, et al.
Neurology|July 1, 1981
Carnitine palmityl transferase deficiency: clinical variability, carrier detection, and autosomal-recessive inheritanceC Angelini, L Freddo, P Battistella, et al.
Pageof 54