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Marika Pane

Showing results (81-90 of 221) with videos related to

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Journal of Neuromuscular Diseases|May 24, 2021
Oral and Swallowing Abilities Tool (OrSAT) for Type 1 SMA Patients: Development of a New ModuleBeatrice Berti, Lavinia Fanelli, Roberto de Sanctis, et al.
Neuropediatrics|December 25, 2014
Cardiac function in types II and III spinal muscular atrophy: should we change standards of care?Flaviana Bianco, Marika Pane, Adele D'Amico, et al.
Neurology. Genetics|May 25, 2026
Compound Heterozygous <i>COA7</i> Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 SiblingsGianpaolo Cicala, Elisa Rolleri, Beatrice Berti, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|December 5, 2006
Visual development in infants with prenatal post-haemorrhagic ventricular dilatationDaniela Ricci, Rita Luciano, Giovanni Baranello, et al.
The Journal of Pediatrics|May 8, 2012
Attention deficit hyperactivity disorder and cognitive function in Duchenne muscular dystrophy: phenotype-genotype correlationMarika Pane, Maria Elena Lombardo, Paolo Alfieri, et al.
International Journal of Language & Communication Disorders|November 20, 2023
Validation and cross-cultural adaptation of the Italian version of the paediatric eating assessment tool (I-PEDI-EAT-10) in genetic syndromesRoberta Onesimo, Elisabetta Sforza, Elizabeth Katherine Anna Triumbari, et al.
Plos One|January 17, 2018
Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment?Stefano Vicari, Giorgia Piccini, Eugenio Mercuri, et al.
Plos One|June 21, 2018
Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophyClaudia Brogna, Lara Cristiano, Tommaso Tartaglione, et al.
Archives of Disease in Childhood|June 17, 2025
Identification and treatment of neurodevelopmental and mental disorders in boys and adults with Duchenne muscular dystrophy: a cohort studyClaudia Brogna, Federica Moriconi, Anna Capasso, et al.
Journal of Neuromuscular Diseases|November 19, 2023
Can the CHOP-INTEND be used as An Outcome Measure in the First Months of Age? Implications for Clinical Trials and Real World DataCostanza Cutrona, Roberto de Sanctis, Giorgia Coratti, et al.
Pageof 23

Showing results (81-90 of 221) with videos related to

Sort By:
Pageof 23
Journal of Neuromuscular Diseases|May 24, 2021
Oral and Swallowing Abilities Tool (OrSAT) for Type 1 SMA Patients: Development of a New ModuleBeatrice Berti, Lavinia Fanelli, Roberto de Sanctis, et al.
Neuropediatrics|December 25, 2014
Cardiac function in types II and III spinal muscular atrophy: should we change standards of care?Flaviana Bianco, Marika Pane, Adele D'Amico, et al.
Neurology. Genetics|May 25, 2026
Compound Heterozygous <i>COA7</i> Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 SiblingsGianpaolo Cicala, Elisa Rolleri, Beatrice Berti, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|December 5, 2006
Visual development in infants with prenatal post-haemorrhagic ventricular dilatationDaniela Ricci, Rita Luciano, Giovanni Baranello, et al.
The Journal of Pediatrics|May 8, 2012
Attention deficit hyperactivity disorder and cognitive function in Duchenne muscular dystrophy: phenotype-genotype correlationMarika Pane, Maria Elena Lombardo, Paolo Alfieri, et al.
International Journal of Language & Communication Disorders|November 20, 2023
Validation and cross-cultural adaptation of the Italian version of the paediatric eating assessment tool (I-PEDI-EAT-10) in genetic syndromesRoberta Onesimo, Elisabetta Sforza, Elizabeth Katherine Anna Triumbari, et al.
Plos One|January 17, 2018
Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment?Stefano Vicari, Giorgia Piccini, Eugenio Mercuri, et al.
Plos One|June 21, 2018
Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophyClaudia Brogna, Lara Cristiano, Tommaso Tartaglione, et al.
Archives of Disease in Childhood|June 17, 2025
Identification and treatment of neurodevelopmental and mental disorders in boys and adults with Duchenne muscular dystrophy: a cohort studyClaudia Brogna, Federica Moriconi, Anna Capasso, et al.
Journal of Neuromuscular Diseases|November 19, 2023
Can the CHOP-INTEND be used as An Outcome Measure in the First Months of Age? Implications for Clinical Trials and Real World DataCostanza Cutrona, Roberto de Sanctis, Giorgia Coratti, et al.
Pageof 23