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Developmental Medicine and Child Neurology
|
September 15, 2015
Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations
Valeria Ricotti, William P L Mandy, Mariacristina Scoto, et al.
Neuromuscular Disorders : NMD
|
September 5, 2018
Does albuterol have an effect on neuromuscular junction dysfunction in spinal muscular atrophy?
Maria Carmela Pera, Marco Luigetti, Serena Sivo, et al.
Annals of Clinical and Translational Neurology
|
November 4, 2020
Nusinersen in type 0 spinal muscular atrophy: should we treat?
Eloisa Tiberi, Simonetta Costa, Marika Pane, et al.
Neuromuscular Disorders : NMD
|
August 12, 2017
Longitudinal assessments in discordant twins with SMA
Marika Pane, Leonardo Lapenta, Emanuela Abiusi, et al.
Epilepsia
|
August 16, 2003
Electroclinical patterns and evolution of epilepsy in the 4p- syndrome
Domenica Battaglia, Giuseppe Zampino, Marcella Zollino, et al.
Neuromuscular Disorders : NMD
|
September 18, 2012
Muscle MRI in Becker muscular dystrophy
Giorgio Tasca, Elisabetta Iannaccone, Mauro Monforte, et al.
Neuromuscular Disorders : NMD
|
April 19, 2008
Feeding problems and malnutrition in spinal muscular atrophy type II
Sonia Messina, Marika Pane, Paola De Rose, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
October 29, 2024
Transition and management of patients with Duchenne Muscular Dystrophy: a narrative review based on Italian experts' opinion and real-world experience
Carlotta Spagnoli, Rachele Adorisio, Luca Bello, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 26, 2024
Continuitiy of care with ataluren in Duchenne Muscular Dystrophy patients with nonsense mutations after loss of ambulation. Personal experience
Carlotta Spagnoli, Rachele Adorisio, Luca Bello, et al.
Orphanet Journal of Rare Diseases
|
October 14, 2021
Motor function in type 2 and 3 SMA patients treated with Nusinersen: a critical review and meta-analysis
Giorgia Coratti, Costanza Cutrona, Maria Carmela Pera, et al.
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Search research articles
Search
Showing results (31-40 of 220) with videos related to
Sort By:
Page
of 22
Developmental Medicine and Child Neurology
|
September 15, 2015
Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations
Valeria Ricotti, William P L Mandy, Mariacristina Scoto, et al.
Neuromuscular Disorders : NMD
|
September 5, 2018
Does albuterol have an effect on neuromuscular junction dysfunction in spinal muscular atrophy?
Maria Carmela Pera, Marco Luigetti, Serena Sivo, et al.
Annals of Clinical and Translational Neurology
|
November 4, 2020
Nusinersen in type 0 spinal muscular atrophy: should we treat?
Eloisa Tiberi, Simonetta Costa, Marika Pane, et al.
Neuromuscular Disorders : NMD
|
August 12, 2017
Longitudinal assessments in discordant twins with SMA
Marika Pane, Leonardo Lapenta, Emanuela Abiusi, et al.
Epilepsia
|
August 16, 2003
Electroclinical patterns and evolution of epilepsy in the 4p- syndrome
Domenica Battaglia, Giuseppe Zampino, Marcella Zollino, et al.
Neuromuscular Disorders : NMD
|
September 18, 2012
Muscle MRI in Becker muscular dystrophy
Giorgio Tasca, Elisabetta Iannaccone, Mauro Monforte, et al.
Neuromuscular Disorders : NMD
|
April 19, 2008
Feeding problems and malnutrition in spinal muscular atrophy type II
Sonia Messina, Marika Pane, Paola De Rose, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
October 29, 2024
Transition and management of patients with Duchenne Muscular Dystrophy: a narrative review based on Italian experts' opinion and real-world experience
Carlotta Spagnoli, Rachele Adorisio, Luca Bello, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 26, 2024
Continuitiy of care with ataluren in Duchenne Muscular Dystrophy patients with nonsense mutations after loss of ambulation. Personal experience
Carlotta Spagnoli, Rachele Adorisio, Luca Bello, et al.
Orphanet Journal of Rare Diseases
|
October 14, 2021
Motor function in type 2 and 3 SMA patients treated with Nusinersen: a critical review and meta-analysis
Giorgia Coratti, Costanza Cutrona, Maria Carmela Pera, et al.
Page
of 22