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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 19, 2006
Feeding problems and weight gain in Duchenne muscular dystrophy
Marika Pane, Isabella Vasta, Sonia Messina, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 22, 2011
Infantile spinal muscular atrophy with respiratory distress type I (SMARD 1): an atypical phenotype and review of the literature
Maria F Messina, Sonia Messina, Michele Gaeta, et al.
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.
Neurobiology of Aging
|
February 9, 2010
Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy
M'Hammed Aguennouz, Gian Luca Vita, Sonia Messina, et al.
Free Radical Research
|
July 23, 2005
Oxidative stress in myotonic dystrophy type 1
Antonio Toscano, Sonia Messina, Giuseppe M Campo, et al.
Journal of Neuromuscular Diseases
|
November 18, 2016
Myasthenia Gravis: Unusual Presentations and Diagnostic Pitfalls
Carmelo Rodolico, Daniela Parisi, Simona Portaro, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 5, 2019
The role of rehabilitation in the management of late-onset Pompe disease: a narrative review of the level of evidence
Giovanni Iolascon, Michele Vitacca, Elena Carraro, 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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 8, 2019
Adapted physical activity and therapeutic exercise in late-onset Pompe disease (LOPD): a two-step rehabilitative approach
Giovanni Iolascon, Michele Vitacca, Elena Carraro, et al.
Journal of Endocrinological Investigation
|
September 15, 2021
Bone health in Duchenne muscular dystrophy: clinical and biochemical correlates
Antonino Catalano, Gian Luca Vita, Federica Bellone, et al.
Page
of 17
Search research articles
Search
Showing results (21-30 of 162) with videos related to
Sort By:
Page
of 17
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 19, 2006
Feeding problems and weight gain in Duchenne muscular dystrophy
Marika Pane, Isabella Vasta, Sonia Messina, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 22, 2011
Infantile spinal muscular atrophy with respiratory distress type I (SMARD 1): an atypical phenotype and review of the literature
Maria F Messina, Sonia Messina, Michele Gaeta, et al.
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.
Neurobiology of Aging
|
February 9, 2010
Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy
M'Hammed Aguennouz, Gian Luca Vita, Sonia Messina, et al.
Free Radical Research
|
July 23, 2005
Oxidative stress in myotonic dystrophy type 1
Antonio Toscano, Sonia Messina, Giuseppe M Campo, et al.
Journal of Neuromuscular Diseases
|
November 18, 2016
Myasthenia Gravis: Unusual Presentations and Diagnostic Pitfalls
Carmelo Rodolico, Daniela Parisi, Simona Portaro, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 5, 2019
The role of rehabilitation in the management of late-onset Pompe disease: a narrative review of the level of evidence
Giovanni Iolascon, Michele Vitacca, Elena Carraro, 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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 8, 2019
Adapted physical activity and therapeutic exercise in late-onset Pompe disease (LOPD): a two-step rehabilitative approach
Giovanni Iolascon, Michele Vitacca, Elena Carraro, et al.
Journal of Endocrinological Investigation
|
September 15, 2021
Bone health in Duchenne muscular dystrophy: clinical and biochemical correlates
Antonino Catalano, Gian Luca Vita, Federica Bellone, et al.
Page
of 17