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Frontiers in Molecular Neuroscience|October 4, 2023
The miRNA transcriptome of cerebrospinal fluid in preterm infants reveals the signaling pathways that promote reactive gliosis following cerebral hemorrhageAndriana Gialeli, Robert Spaull, Torsten Plösch, et al.Developmental Medicine and Child Neurology|December 1, 2019
The expanding spectrum of movement disorders in genetic epilepsiesApostolos Papandreou, Federica Rachele Danti, Robert Spaull, et al.International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 15, 2019
Exosomes populate the cerebrospinal fluid of preterm infants with post-haemorrhagic hydrocephalusRobert Spaull, Bryony McPherson, Andriana Gialeli, et al.Case Reports in Pediatrics|September 17, 2025
Hypotonia, Ataxia, Developmental Delay and Tooth Enamel Defect Syndrome (HADDTS) due to a Heterozygous de Novo Missense Variant in <i>CTBP1</i> Identified via Whole Genome SequencingSilvia Beatriz Sanchez Marco, Emily Pardington, Marie Monaghan, et al.Neurology|July 8, 2024
Evolution of Movement Disorders in Patients With CLN2-Batten Disease Treated With Enzyme Replacement TherapyRobert Spaull, Audrey K Soo, Spyros Batzios, et al.Journal of Pediatric Orthopedics|October 23, 2023
Femur Fractures in 5 Individuals With Pantothenate Kinase-associated Neurodegeneration: The Role of Dystonia and Suggested ManagementLaken Behrndt, Allison Gregory, Katrina Wakeman, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 14, 2025
Development and Preliminary Validation of a Parkinsonism-Dystonia Scale for Infants and Young ChildrenRoser Pons, Toni S Pearson, Belen Perez-Dueñas, et al.Archives of Disease in Childhood|November 11, 2025
Transdermal clonidine patch use in the management of childhood hypertonia: a cross-sectional UK-wide service evaluationDaniel E Lumsden, Robert Spaull, Sarah Abernethy, et al.Neurology|January 28, 2021
<i>RHOBTB2</i> Mutations Expand the Phenotypic Spectrum of Alternating Hemiplegia of ChildhoodSara Zagaglia, Dora Steel, S Krithika, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 25, 2022
MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe DystoniaKimberley M Reid, Robert Spaull, Smrithi Salian, et al.Pageof 2