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Child: Care, Health and Development|September 27, 2018
Seeking normality: Parents' experiences of childhood strokeChristopher McKevitt, Marta Topor, Anna Panton, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
Generalized arterial calcification of infancy: phenotypic spectrum among three siblings including one case without obvious arterial calcificationsNomazulu Dlamini, Miranda Splitt, Anne Durkan, et al.
Developmental Medicine and Child Neurology|January 20, 2011
Congenital lower brachial plexus palsy due to cervical ribsArchana Desurkar, Kerry Mills, Matthew Pitt, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 2, 2018
Self-reported needs after pediatric strokeAnne L Gordon, Loan Nguyen, Anna Panton, et al.
Neuromuscular Disorders : NMD|January 2, 2021
Genetic neuropathies presenting with CIDP-like features in childhoodMiguel A Fernandez-Garcia, Georg M Stettner, Maria Kinali, et al.
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.
Neuromuscular Disorders : NMD|October 8, 2024
Spinal presentations in children with spinal muscular atrophy type 1 following gene therapy treatment with onasemnogene abeparvovec - The SMA REACH UK network experienceAmy Wolfe, Jennie Sheehan, Alex Schofield, et al.
Human Mutation|July 17, 2010
Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutationsJames J Cox, Jony Sheynin, Zamir Shorer, et al.
Neuromuscular Disorders : NMD|August 7, 2024
Risk-benefit profile of onasemnogene abeparvovec in older and heavier children with spinal muscular atrophy type 1Rebecca Finnegan, Adnan Manzur, Pinki Munot, et al.
Neuromuscular Disorders : NMD|July 14, 2010
Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectinKatharine Forrest, Jemima E Mellerio, Stephanie Robb, et al.
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