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Luisa Politano

Showing results (41-50 of 176) with videos related to

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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 11, 2021
Impact of the COVID-19 pandemic on rehabilitation setting. Part 1: professionals' views on the changes in routine care provided by a rehabilitation centre for patients with muscle diseasesGiulia Citarelli, Ciro Garofalo, Maria Grazia Esposito, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 24, 2012
Genetic counseling in Pompe diseaseAntonella Taglia, Esther Picillo, Paola D'Ambrosio, et al.
Biomolecules|April 27, 2024
Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the <i>KCNJ2</i> Gene-A New Family Case ReportMaria Elena Onore, Esther Picillo, Paola D'Ambrosio, et al.
Human Mutation|November 13, 2007
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2HValentina Saccone, Michela Palmieri, Luigia Passamano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 8, 2024
Treatment with ataluren in four symptomatic Duchenne carriers. A pilot studyAmir Dori, Marianna Scutifero, Luigia Passamano, et al.
Ophthalmology|June 5, 2013
Intraocular pressure in patients with muscular dystrophiesNicola Rosa, Michele Lanza, Maddalena de Bernardo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|January 20, 2022
How to define and enhance diagnostic and assistance pathways in neuromuscular diseases during the COVID-19 pandemic: the concept of networkGuja Astrea, Gemma Marinella, Caterina Agosto, et al.
Ophthalmology|November 21, 2008
Intraocular pressure and corneal biomechanical properties in patients with myotonic dystrophyNicola Rosa, Michele Lanza, Maria Borrelli, et al.
Journal of Cardiovascular Electrophysiology|September 3, 2015
The Role of the Atrial Electromechanical Delay in Predicting Atrial Fibrillation in Myotonic Dystrophy Type 1 PatientsVincenzo Russo, Anna Rago, Carmine Ciardiello, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 24, 2023
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literatureAntonella Pizza, Esther Picillo, Maria Elena Onore, et al.
Pageof 18

Showing results (41-50 of 176) with videos related to

Sort By:
Pageof 18
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 11, 2021
Impact of the COVID-19 pandemic on rehabilitation setting. Part 1: professionals' views on the changes in routine care provided by a rehabilitation centre for patients with muscle diseasesGiulia Citarelli, Ciro Garofalo, Maria Grazia Esposito, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 24, 2012
Genetic counseling in Pompe diseaseAntonella Taglia, Esther Picillo, Paola D'Ambrosio, et al.
Biomolecules|April 27, 2024
Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the <i>KCNJ2</i> Gene-A New Family Case ReportMaria Elena Onore, Esther Picillo, Paola D'Ambrosio, et al.
Human Mutation|November 13, 2007
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2HValentina Saccone, Michela Palmieri, Luigia Passamano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 8, 2024
Treatment with ataluren in four symptomatic Duchenne carriers. A pilot studyAmir Dori, Marianna Scutifero, Luigia Passamano, et al.
Ophthalmology|June 5, 2013
Intraocular pressure in patients with muscular dystrophiesNicola Rosa, Michele Lanza, Maddalena de Bernardo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|January 20, 2022
How to define and enhance diagnostic and assistance pathways in neuromuscular diseases during the COVID-19 pandemic: the concept of networkGuja Astrea, Gemma Marinella, Caterina Agosto, et al.
Ophthalmology|November 21, 2008
Intraocular pressure and corneal biomechanical properties in patients with myotonic dystrophyNicola Rosa, Michele Lanza, Maria Borrelli, et al.
Journal of Cardiovascular Electrophysiology|September 3, 2015
The Role of the Atrial Electromechanical Delay in Predicting Atrial Fibrillation in Myotonic Dystrophy Type 1 PatientsVincenzo Russo, Anna Rago, Carmine Ciardiello, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 24, 2023
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literatureAntonella Pizza, Esther Picillo, Maria Elena Onore, et al.
Pageof 18