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Luisa Politano

Showing results (71-80 of 176) with videos related to

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Genes|January 21, 2023
Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern ItalyEmanuela Viggiano, Esther Picillo, Luigia Passamano, et al.
Ophthalmology|August 31, 2010
Low intraocular pressure resulting from ciliary body detachment in patients with myotonic dystrophyNicola Rosa, Michele Lanza, Maria Borrelli, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 17, 2019
Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal resultsAlberto Palladino, Andrea A Papa, Salvatore Morra, et al.
Aging Cell|December 11, 2024
Aging research from bench to bedside and beyond: What we learned from Sammy BassoGiovanna Lattanzi, Chiara Lanzuolo, Eleonora Cugudda, et al.
Human Mutation|June 15, 2005
Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosisStefan J White, Shirley Uitte de Willige, Dennis Verbove, et al.
The Journal of Molecular Diagnostics : JMD|December 5, 2009
One hundred twenty-one dystrophin point mutations detected from stored DNA samples by combinatorial denaturing high-performance liquid chromatographyAnnalaura Torella, Amelia Trimarco, Francesca Del Vecchio Blanco, et al.
Journal of Cardiovascular Electrophysiology|October 4, 2019
SERUM cardiac-specific biomarkers and atrial fibrillation in myotonic dystrophy type IVincenzo Russo, Anna Rago, Luigi Atripaldi, et al.
Neuromuscular Disorders : NMD|February 12, 2021
Prevalence of atrial fibrillation in myotonic dystrophy type 1: A systematic reviewVincenzo Russo, Andrea Antonio Papa, Michele Lioncino, et al.
Ophthalmology|December 9, 2009
Corneal thickness and endothelial cell characteristics in patients with myotonic dystrophyNicola Rosa, Michele Lanza, Maria Borrelli, et al.
Neuromuscular Disorders : NMD|February 13, 2010
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophyGerardo Nigro, Vincenzo Russo, Vega Maria Ventriglia, et al.
Pageof 18

Showing results (71-80 of 176) with videos related to

Sort By:
Pageof 18
Genes|January 21, 2023
Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern ItalyEmanuela Viggiano, Esther Picillo, Luigia Passamano, et al.
Ophthalmology|August 31, 2010
Low intraocular pressure resulting from ciliary body detachment in patients with myotonic dystrophyNicola Rosa, Michele Lanza, Maria Borrelli, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 17, 2019
Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal resultsAlberto Palladino, Andrea A Papa, Salvatore Morra, et al.
Aging Cell|December 11, 2024
Aging research from bench to bedside and beyond: What we learned from Sammy BassoGiovanna Lattanzi, Chiara Lanzuolo, Eleonora Cugudda, et al.
Human Mutation|June 15, 2005
Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosisStefan J White, Shirley Uitte de Willige, Dennis Verbove, et al.
The Journal of Molecular Diagnostics : JMD|December 5, 2009
One hundred twenty-one dystrophin point mutations detected from stored DNA samples by combinatorial denaturing high-performance liquid chromatographyAnnalaura Torella, Amelia Trimarco, Francesca Del Vecchio Blanco, et al.
Journal of Cardiovascular Electrophysiology|October 4, 2019
SERUM cardiac-specific biomarkers and atrial fibrillation in myotonic dystrophy type IVincenzo Russo, Anna Rago, Luigi Atripaldi, et al.
Neuromuscular Disorders : NMD|February 12, 2021
Prevalence of atrial fibrillation in myotonic dystrophy type 1: A systematic reviewVincenzo Russo, Andrea Antonio Papa, Michele Lioncino, et al.
Ophthalmology|December 9, 2009
Corneal thickness and endothelial cell characteristics in patients with myotonic dystrophyNicola Rosa, Michele Lanza, Maria Borrelli, et al.
Neuromuscular Disorders : NMD|February 13, 2010
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophyGerardo Nigro, Vincenzo Russo, Vega Maria Ventriglia, et al.
Pageof 18