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Archives of Neurology|September 14, 2011
Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutationsAndrea Klein, Heinz Jungbluth, Emma Clement, et al.
BMC Medical Genetics|March 15, 2019
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case reportTeresa Sprovieri, Carmine Ungaro, Serena Sivo, et al.
CNS Drugs|January 26, 2022
Restoration of Nusinersen Levels Following Treatment Interruption in People With Spinal Muscular Atrophy: Simulations Based on a Population Pharmacokinetic ModelDrew MacCannell, Zdenek Berger, Janbernd Kirschner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 9, 2021
Extra-uterine growth restriction in preterm infants: Neurodevelopmental outcomes according to different definitionsDomenico Umberto De Rose, Francesco Cota, Francesca Gallini, et al.
Lancet (London, England)|March 7, 2003
Origin and timing of brain lesions in term infants with neonatal encephalopathyFrances Cowan, Mary Rutherford, Floris Groenendaal, et al.
Early Human Development|February 16, 2010
Visual performance and brain structures in the developing brain of pre-term infantsLuca Antonio Ramenghi, Daniela Ricci, Eugenio Mercuri, et al.
Neuropediatrics|September 23, 2010
Quality of life in parents of children with cerebral palsy: is it influenced by the child's behaviour?D M Romeo, M Cioni, A Distefano, et al.
Neuromuscular Disorders : NMD|March 29, 2005
Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathyEugenio Mercuri, Anne Lampe, Joanna Allsop, et al.
Plos One|November 26, 2024
Correction: Neural substrates of neuropsychological profiles in dystrophynopathies: A pilot study of diffusion tractography imagingLaura Biagi, Sara Lenzi, Emilio Cipriano, et al.
Epilepsia|August 16, 2003
Electroclinical patterns and evolution of epilepsy in the 4p- syndromeDomenica Battaglia, Giuseppe Zampino, Marcella Zollino, et al.
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