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Neurology
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August 28, 2019
Long-term progression in type II spinal muscular atrophy: A retrospective observational study
Eugenio Mercuri, Simona Lucibello, Maria Carmela Pera, et al.
Pediatric Pulmonology
|
May 13, 2020
Ultrasound assessment of diaphragmatic function in type 1 spinal muscular atrophy
Danilo Buonsenso, Beatrice Berti, Concetta Palermo, et al.
European Journal of Pediatrics
|
August 18, 2025
Development of the "SMA NNE," a short neonatal neurological examination for newborns with spinal muscular atrophy
Eugenio Mercuri, Giorgia Coratti, Costanza Cutrona, et al.
Italian Journal of Pediatrics
|
March 15, 2026
Cross-cultural adaptation of the Italian version of the "Child and Youth Mental Health Instrument for Developmental Disabilities" (I-ChYMH-DD)
Elisabetta Sforza, Chiara Leoni, Elena De Rosa, et al.
Neuromuscular Disorders : NMD
|
November 28, 2017
Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy
Roberto De Sanctis, Marika Pane, Giorgia Coratti, et al.
Neuromuscular Disorders : NMD
|
August 15, 2017
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction
Maria Carmela Pera, Marco Luigetti, Marika Pane, et al.
Early Human Development
|
February 28, 2006
Thalamic atrophy in infants with PVL and cerebral visual impairment
Daniela Ricci, Shirley Anker, Frances Cowan, et al.
Neurology
|
March 8, 2019
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild calf-predominant myopathy
Manu Jokela, Giorgio Tasca, Anna Vihola, et al.
Early Human Development
|
July 11, 2008
Neurological examination of preterm infants at term equivalent age
Daniela Ricci, Domenico M M Romeo, Leena Haataja, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
December 11, 2020
Respiratory function and therapeutic expectations in DMD: families experience and perspective
Claudia Brogna, Simona Lucibello, Giorgia Coratti, et al.
Page
of 23
Search research articles
Search
Showing results (71-80 of 221) with videos related to
Sort By:
Page
of 23
Neurology
|
August 28, 2019
Long-term progression in type II spinal muscular atrophy: A retrospective observational study
Eugenio Mercuri, Simona Lucibello, Maria Carmela Pera, et al.
Pediatric Pulmonology
|
May 13, 2020
Ultrasound assessment of diaphragmatic function in type 1 spinal muscular atrophy
Danilo Buonsenso, Beatrice Berti, Concetta Palermo, et al.
European Journal of Pediatrics
|
August 18, 2025
Development of the "SMA NNE," a short neonatal neurological examination for newborns with spinal muscular atrophy
Eugenio Mercuri, Giorgia Coratti, Costanza Cutrona, et al.
Italian Journal of Pediatrics
|
March 15, 2026
Cross-cultural adaptation of the Italian version of the "Child and Youth Mental Health Instrument for Developmental Disabilities" (I-ChYMH-DD)
Elisabetta Sforza, Chiara Leoni, Elena De Rosa, et al.
Neuromuscular Disorders : NMD
|
November 28, 2017
Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy
Roberto De Sanctis, Marika Pane, Giorgia Coratti, et al.
Neuromuscular Disorders : NMD
|
August 15, 2017
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction
Maria Carmela Pera, Marco Luigetti, Marika Pane, et al.
Early Human Development
|
February 28, 2006
Thalamic atrophy in infants with PVL and cerebral visual impairment
Daniela Ricci, Shirley Anker, Frances Cowan, et al.
Neurology
|
March 8, 2019
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild calf-predominant myopathy
Manu Jokela, Giorgio Tasca, Anna Vihola, et al.
Early Human Development
|
July 11, 2008
Neurological examination of preterm infants at term equivalent age
Daniela Ricci, Domenico M M Romeo, Leena Haataja, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
December 11, 2020
Respiratory function and therapeutic expectations in DMD: families experience and perspective
Claudia Brogna, Simona Lucibello, Giorgia Coratti, et al.
Page
of 23