Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

L Politano

Showing results (1-10 of 36) with videos related to

Pageof 4
Sort By:
Clinical Genetics|November 1, 2012
Comparison of X-chromosome inactivation in Duchenne muscle/myocardium-manifesting carriers, non-manifesting carriers and related daughtersE Viggiano, E Picillo, A Cirillo, et al.
Clinical Genetics|April 5, 2017
Galactose-1-phosphate uridyltransferase deficiency: A literature review of the putative mechanisms of short and long-term complications and allelic variantsE Viggiano, A Marabotti, L Politano, et al.
International Journal of Cardiology|March 1, 1992
The cardiomyopathy of Duchenne/Becker consultandsL I Comi, G Nigro, L Politano, et al.
Archivio Per Le Scienze Mediche|July 1, 1977
[A new dynamic index in the clinical evaluation of muscle efficiency]L I Comi, L Politano, F P Inglese, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 29, 2009
Usefulness of heart rate variability as a predictor of sudden cardiac death in muscular dystrophiesL Politano, A Palladino, G Nigro, et al.
International Journal of Cardiology|March 1, 1990
The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophyG Nigro, L I Comi, L Politano, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Mutation of dystrophin gene and cardiomyopathyG Nigro, L Politano, V Nigro, et al.
Archivio Per Le Scienze Mediche|July 1, 1978
[The rheumatic index. A new electrocardiographic parameter in evaluation of rheumatic activity]G Nigro, L I Comi, M A Giugliano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 21, 2004
Cardiomyopathies: diagnosis of types and stagesG Nigro, L I Comi, Ge Nigro, et al.
Human Molecular Genetics|October 1, 1992
Detection of a nonsense mutation in the dystrophin gene by multiple SSCPV Nigro, L Politano, G Nigro, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Clinical Genetics|November 1, 2012
Comparison of X-chromosome inactivation in Duchenne muscle/myocardium-manifesting carriers, non-manifesting carriers and related daughtersE Viggiano, E Picillo, A Cirillo, et al.
Clinical Genetics|April 5, 2017
Galactose-1-phosphate uridyltransferase deficiency: A literature review of the putative mechanisms of short and long-term complications and allelic variantsE Viggiano, A Marabotti, L Politano, et al.
International Journal of Cardiology|March 1, 1992
The cardiomyopathy of Duchenne/Becker consultandsL I Comi, G Nigro, L Politano, et al.
Archivio Per Le Scienze Mediche|July 1, 1977
[A new dynamic index in the clinical evaluation of muscle efficiency]L I Comi, L Politano, F P Inglese, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 29, 2009
Usefulness of heart rate variability as a predictor of sudden cardiac death in muscular dystrophiesL Politano, A Palladino, G Nigro, et al.
International Journal of Cardiology|March 1, 1990
The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophyG Nigro, L I Comi, L Politano, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Mutation of dystrophin gene and cardiomyopathyG Nigro, L Politano, V Nigro, et al.
Archivio Per Le Scienze Mediche|July 1, 1978
[The rheumatic index. A new electrocardiographic parameter in evaluation of rheumatic activity]G Nigro, L I Comi, M A Giugliano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 21, 2004
Cardiomyopathies: diagnosis of types and stagesG Nigro, L I Comi, Ge Nigro, et al.
Human Molecular Genetics|October 1, 1992
Detection of a nonsense mutation in the dystrophin gene by multiple SSCPV Nigro, L Politano, G Nigro, et al.
Pageof 4