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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 27, 2013
On a case of respiratory failure due to diaphragmatic paralysis and dilated cardiomyopathy in a patient with nemaline myopathy
Antonella Taglia, Paola D'Ambrosio, Alberto Palladino, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 5, 2019
Therapeutic approach with Ataluren in Duchenne symptomatic carriers with nonsense mutations in dystrophin gene. Results of a 9-month follow-up in a case report
Paola D'Ambrosio, Chiara Orsini, Vincenzo Nigro, et al.
Human Genetics
|
April 22, 2016
Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy
Emanuela Viggiano, Manuela Ergoli, Esther Picillo, et al.
Journal of Neuromuscular Diseases
|
May 24, 2021
Have Duchenne Muscular Dystrophy Patients an Increased Cancer Risk?
Gian Luca Vita, Luisa Politano, Angela Berardinelli, et al.
Anadolu Kardiyoloji Dergisi : AKD = the Anatolian Journal of Cardiology
|
June 26, 2012
Early onset "electrical" heart failure in myotonic dystrophy type 1 patient: the role of ICD biventricular pacing
Vincenzo Russo, Anna Rago, Antonello D'Andrea, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 14, 2022
Autosomal dominant Ullrich congenital muscular dystrophy due to a <i>de novo</i> mutation in <i>COL6A3</i> gene. A case report
Esther Picillo, Annalaura Torella, Luigia Passamano, et al.
Molecular Reproduction and Development
|
December 17, 2019
Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function
Manuela Ergoli, Massimo Venditti, Esther Picillo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 14, 2022
Impact of the COVID-19 pandemic on neuromuscular rehabilitation setting. Part 2: patients and families' views on the received health care during the pandemic
Lorenza Magliano, Giulia Citarelli, Maria Grazia Esposito, et al.
Intractable & Rare Diseases Research
|
June 6, 2017
Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series
Andrea Antonio Papa, Paola D'Ambrosio, Roberta Petillo, et al.
Cases Journal
|
January 12, 2010
Anterior capsule phimosis and capsular block syndrome in a patient with Steinert myotonic dystrophy: a case report
Nicola Rosa, Michele Lanza, Maddalena De Bernardo, et al.
Page
of 18
Search research articles
Search
Showing results (21-30 of 176) with videos related to
Sort By:
Page
of 18
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 27, 2013
On a case of respiratory failure due to diaphragmatic paralysis and dilated cardiomyopathy in a patient with nemaline myopathy
Antonella Taglia, Paola D'Ambrosio, Alberto Palladino, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 5, 2019
Therapeutic approach with Ataluren in Duchenne symptomatic carriers with nonsense mutations in dystrophin gene. Results of a 9-month follow-up in a case report
Paola D'Ambrosio, Chiara Orsini, Vincenzo Nigro, et al.
Human Genetics
|
April 22, 2016
Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy
Emanuela Viggiano, Manuela Ergoli, Esther Picillo, et al.
Journal of Neuromuscular Diseases
|
May 24, 2021
Have Duchenne Muscular Dystrophy Patients an Increased Cancer Risk?
Gian Luca Vita, Luisa Politano, Angela Berardinelli, et al.
Anadolu Kardiyoloji Dergisi : AKD = the Anatolian Journal of Cardiology
|
June 26, 2012
Early onset "electrical" heart failure in myotonic dystrophy type 1 patient: the role of ICD biventricular pacing
Vincenzo Russo, Anna Rago, Antonello D'Andrea, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 14, 2022
Autosomal dominant Ullrich congenital muscular dystrophy due to a <i>de novo</i> mutation in <i>COL6A3</i> gene. A case report
Esther Picillo, Annalaura Torella, Luigia Passamano, et al.
Molecular Reproduction and Development
|
December 17, 2019
Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function
Manuela Ergoli, Massimo Venditti, Esther Picillo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 14, 2022
Impact of the COVID-19 pandemic on neuromuscular rehabilitation setting. Part 2: patients and families' views on the received health care during the pandemic
Lorenza Magliano, Giulia Citarelli, Maria Grazia Esposito, et al.
Intractable & Rare Diseases Research
|
June 6, 2017
Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series
Andrea Antonio Papa, Paola D'Ambrosio, Roberta Petillo, et al.
Cases Journal
|
January 12, 2010
Anterior capsule phimosis and capsular block syndrome in a patient with Steinert myotonic dystrophy: a case report
Nicola Rosa, Michele Lanza, Maddalena De Bernardo, et al.
Page
of 18