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Giovanni Baranello

Showing results (31-40 of 172) with videos related to

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American Journal of Respiratory and Critical Care Medicine|April 15, 2022
Can Breathing Pattern Assessment Predict the Need of Ventilatory Support in Treated Infants with Spinal Muscular Atrophy Type 1?Antonella LoMauro, Chiara Mastella, Mariacristina Scoto, et al.
Muscle & Nerve|February 27, 2025
Characteristics of Patients With Spinal Muscular Atrophy Who Have Switched Treatments: A Multi-Center Experience in the United KingdomEmer O'Reilly, Georgia Stimpson, Annemarie Rohwer, et al.
Journal of the Peripheral Nervous System : JPNS|October 19, 2011
Outcome measures for Charcot-Marie-Tooth disease: clinical and neurofunctional assessment in childrenEmanuela Pagliano, Isabella Moroni, Giovanni Baranello, et al.
Journal of Child Neurology|April 25, 2013
Partial Trisomy 13 and Partial Monosomy 8 Mosaicism Secondary to an Unbalanced De Novo Translocation: Highlighting an Uncommon Chromosomal AbnormalityGiovanni Baranello, Claudia Cesaretti, Fabio Zambonin, et al.
Iranian Journal of Child Neurology|August 11, 2025
The Visual Function Classification System: Translation, Validity, and Reliability of the Persian Version for Individuals with Cerebral PalsyMarzieh Pashmdarfard, Malek Amini, Mahnaz Hejazi-Shirmard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2018
Outcome measures for children with movement disordersEmanuela Pagliano, Giovanni Baranello, Riccardo Masson, et al.
Clinical Nutrition (Edinburgh, Scotland)|November 29, 2016
Spinal Muscular Atrophy, types I and II: What are the differences in body composition and resting energy expenditure?Simona Bertoli, Ramona De Amicis, Chiara Mastella, et al.
Developmental Medicine and Child Neurology|April 6, 2022
Peak functional ability and age at loss of ambulation in Duchenne muscular dystrophyAlberto A Zambon, Vandana Ayyar Gupta, Deborah Ridout, et al.
IEEE ... International Conference on Rehabilitation Robotics : [Proceedings]|August 18, 2017
Two single cases treated by a new pseudoelastic upper-limb orthosis for secondary dystonia of the youngLorenzo Garavaglia, Emanuela Pagliano, Maria Teresa Arnoldi, et al.
Pediatric Neurology|July 6, 2014
Hyperargininemia: 7-month follow-up under sodium benzoate therapy in an Italian child presenting progressive spastic paraparesis, cognitive decline, and novel mutation in ARG1 geneGiovanni Baranello, Enrico Alfei, Diego Martinelli, et al.
Pageof 18

Showing results (31-40 of 172) with videos related to

Sort By:
Pageof 18
American Journal of Respiratory and Critical Care Medicine|April 15, 2022
Can Breathing Pattern Assessment Predict the Need of Ventilatory Support in Treated Infants with Spinal Muscular Atrophy Type 1?Antonella LoMauro, Chiara Mastella, Mariacristina Scoto, et al.
Muscle & Nerve|February 27, 2025
Characteristics of Patients With Spinal Muscular Atrophy Who Have Switched Treatments: A Multi-Center Experience in the United KingdomEmer O'Reilly, Georgia Stimpson, Annemarie Rohwer, et al.
Journal of the Peripheral Nervous System : JPNS|October 19, 2011
Outcome measures for Charcot-Marie-Tooth disease: clinical and neurofunctional assessment in childrenEmanuela Pagliano, Isabella Moroni, Giovanni Baranello, et al.
Journal of Child Neurology|April 25, 2013
Partial Trisomy 13 and Partial Monosomy 8 Mosaicism Secondary to an Unbalanced De Novo Translocation: Highlighting an Uncommon Chromosomal AbnormalityGiovanni Baranello, Claudia Cesaretti, Fabio Zambonin, et al.
Iranian Journal of Child Neurology|August 11, 2025
The Visual Function Classification System: Translation, Validity, and Reliability of the Persian Version for Individuals with Cerebral PalsyMarzieh Pashmdarfard, Malek Amini, Mahnaz Hejazi-Shirmard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2018
Outcome measures for children with movement disordersEmanuela Pagliano, Giovanni Baranello, Riccardo Masson, et al.
Clinical Nutrition (Edinburgh, Scotland)|November 29, 2016
Spinal Muscular Atrophy, types I and II: What are the differences in body composition and resting energy expenditure?Simona Bertoli, Ramona De Amicis, Chiara Mastella, et al.
Developmental Medicine and Child Neurology|April 6, 2022
Peak functional ability and age at loss of ambulation in Duchenne muscular dystrophyAlberto A Zambon, Vandana Ayyar Gupta, Deborah Ridout, et al.
IEEE ... International Conference on Rehabilitation Robotics : [Proceedings]|August 18, 2017
Two single cases treated by a new pseudoelastic upper-limb orthosis for secondary dystonia of the youngLorenzo Garavaglia, Emanuela Pagliano, Maria Teresa Arnoldi, et al.
Pediatric Neurology|July 6, 2014
Hyperargininemia: 7-month follow-up under sodium benzoate therapy in an Italian child presenting progressive spastic paraparesis, cognitive decline, and novel mutation in ARG1 geneGiovanni Baranello, Enrico Alfei, Diego Martinelli, et al.
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