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Marika Pane

Showing results (71-80 of 221) with videos related to

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Neurology|August 28, 2019
Long-term progression in type II spinal muscular atrophy: A retrospective observational studyEugenio Mercuri, Simona Lucibello, Maria Carmela Pera, et al.
Pediatric Pulmonology|May 13, 2020
Ultrasound assessment of diaphragmatic function in type 1 spinal muscular atrophyDanilo 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 atrophyEugenio 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 atrophyRoberto De Sanctis, Marika Pane, Giorgia Coratti, et al.
Neuromuscular Disorders : NMD|August 15, 2017
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunctionMaria Carmela Pera, Marco Luigetti, Marika Pane, et al.
Early Human Development|February 28, 2006
Thalamic atrophy in infants with PVL and cerebral visual impairmentDaniela Ricci, Shirley Anker, Frances Cowan, et al.
Neurology|March 8, 2019
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild calf-predominant myopathyManu Jokela, Giorgio Tasca, Anna Vihola, et al.
Early Human Development|July 11, 2008
Neurological examination of preterm infants at term equivalent ageDaniela 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 perspectiveClaudia Brogna, Simona Lucibello, Giorgia Coratti, et al.
Pageof 23

Showing results (71-80 of 221) with videos related to

Sort By:
Pageof 23
Neurology|August 28, 2019
Long-term progression in type II spinal muscular atrophy: A retrospective observational studyEugenio Mercuri, Simona Lucibello, Maria Carmela Pera, et al.
Pediatric Pulmonology|May 13, 2020
Ultrasound assessment of diaphragmatic function in type 1 spinal muscular atrophyDanilo 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 atrophyEugenio 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 atrophyRoberto De Sanctis, Marika Pane, Giorgia Coratti, et al.
Neuromuscular Disorders : NMD|August 15, 2017
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunctionMaria Carmela Pera, Marco Luigetti, Marika Pane, et al.
Early Human Development|February 28, 2006
Thalamic atrophy in infants with PVL and cerebral visual impairmentDaniela Ricci, Shirley Anker, Frances Cowan, et al.
Neurology|March 8, 2019
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild calf-predominant myopathyManu Jokela, Giorgio Tasca, Anna Vihola, et al.
Early Human Development|July 11, 2008
Neurological examination of preterm infants at term equivalent ageDaniela 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 perspectiveClaudia Brogna, Simona Lucibello, Giorgia Coratti, et al.
Pageof 23