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Luisa Politano

Showing results (31-40 of 176) with videos related to

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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 8, 2024
A rare co-occurrence of phosphorylase kinase deficiency (GSD type IXd) and alpha-glycosidase deficiency (GSD Type II) in a 53-year-old man presenting with an atypical glycogen storage disease phenotypeEsther Picillo, Maria Elena Onore, Luigia Passamano, et al.
Muscles, Ligaments and Tendons Journal|June 6, 2013
Persistent HyperCKemia in AthletesPaola Brancaccio, Nicola Maffulli, Luisa Politano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 3, 2022
Can symptomatic nmDuchenne carriers benefit from treatment with ataluren? Results of 193-month follow-upAmir Dori, Michela Guglieri, Marianna Scutifero, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 18, 2018
Study of anti-Müllerian hormone levels in patients with Myotonic Dystrophy Type 1. Preliminary resultsManuela Ergoli, Massimo Venditti, Raffaele Dotolo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|January 20, 2022
Can symptomatic nmDuchenne carriers benefit from treatment with ataluren? Results of 193-month follow-upAmir Dori, Michela Guglieri, Marianna Scutifero, et al.
International Journal of Molecular Sciences|December 23, 2022
Bi-Allelic <i>DES</i> Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac FunctionMaria Elena Onore, Marco Savarese, Esther Picillo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 26, 2012
Right atrial preference pacing algorithm in the prevention of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: a long term follow-up studyGerardo Nigro, Vincenzo Russo, Anna Rago, et al.
Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|March 1, 2018
Bachmann bundle pacing reduces atrial electromechanical delay in type 1 myotonic dystrophy patientsVincenzo Russo, Anna Rago, Andrea Antonio Papa, et al.
The Journal of Gene Medicine|March 20, 2017
Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophyEmanuela Viggiano, Esther Picillo, Manuela Ergoli, et al.
Clinical Chemistry|April 12, 2008
Log-PCR: a new tool for immediate and cost-effective diagnosis of up to 85% of dystrophin gene mutationsAmelia Trimarco, Annalaura Torella, Giulio Piluso, et al.
Pageof 18

Showing results (31-40 of 176) with videos related to

Sort By:
Pageof 18
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 8, 2024
A rare co-occurrence of phosphorylase kinase deficiency (GSD type IXd) and alpha-glycosidase deficiency (GSD Type II) in a 53-year-old man presenting with an atypical glycogen storage disease phenotypeEsther Picillo, Maria Elena Onore, Luigia Passamano, et al.
Muscles, Ligaments and Tendons Journal|June 6, 2013
Persistent HyperCKemia in AthletesPaola Brancaccio, Nicola Maffulli, Luisa Politano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 3, 2022
Can symptomatic nmDuchenne carriers benefit from treatment with ataluren? Results of 193-month follow-upAmir Dori, Michela Guglieri, Marianna Scutifero, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 18, 2018
Study of anti-Müllerian hormone levels in patients with Myotonic Dystrophy Type 1. Preliminary resultsManuela Ergoli, Massimo Venditti, Raffaele Dotolo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|January 20, 2022
Can symptomatic nmDuchenne carriers benefit from treatment with ataluren? Results of 193-month follow-upAmir Dori, Michela Guglieri, Marianna Scutifero, et al.
International Journal of Molecular Sciences|December 23, 2022
Bi-Allelic <i>DES</i> Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac FunctionMaria Elena Onore, Marco Savarese, Esther Picillo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 26, 2012
Right atrial preference pacing algorithm in the prevention of paroxysmal atrial fibrillation in myotonic dystrophy type 1 patients: a long term follow-up studyGerardo Nigro, Vincenzo Russo, Anna Rago, et al.
Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|March 1, 2018
Bachmann bundle pacing reduces atrial electromechanical delay in type 1 myotonic dystrophy patientsVincenzo Russo, Anna Rago, Andrea Antonio Papa, et al.
The Journal of Gene Medicine|March 20, 2017
Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophyEmanuela Viggiano, Esther Picillo, Manuela Ergoli, et al.
Clinical Chemistry|April 12, 2008
Log-PCR: a new tool for immediate and cost-effective diagnosis of up to 85% of dystrophin gene mutationsAmelia Trimarco, Annalaura Torella, Giulio Piluso, et al.
Pageof 18