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The American Journal of Hospice & Palliative Care|July 15, 2015
Physician Communication in Pediatric End-of-Life Care: A Simulation StudyLori Brand Bateman, Nancy M Tofil, Marjorie Lee White, et al.
Pediatric Neurology|February 12, 2023
Content Validation of the Movement Disorder-Childhood Rating Scale (MD-CRS) for Dyskinetic Cerebral PalsyDaniel O Claassen, Heather R Riordan, Leon S Dure, et al.
Annals of Neurology|April 29, 2014
UBQLN2 mutation causing heterogeneous X-linked dominant neurodegenerationAkl C Fahed, Barbara McDonough, Cynthia M Gouvion, et al.
Epilepsy & Behavior : E&B|August 14, 2018
Cannabidiol improves frequency and severity of seizures and reduces adverse events in an open-label add-on prospective studyJerzy P Szaflarski, Elizabeth Martina Bebin, Gary Cutter, et al.
Journal of Inherited Metabolic Disease|December 15, 2011
Females experience a more severe disease course in Batten diseaseJennifer Cialone, Heather Adams, Erika F Augustine, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|January 19, 2011
Streptococcal upper respiratory tract infections and exacerbations of tic and obsessive-compulsive symptoms: a prospective longitudinal studyJames F Leckman, Robert A King, Donald L Gilbert, et al.
Human Molecular Genetics|April 25, 2002
Mutations in TITF-1 are associated with benign hereditary choreaGuido J Breedveld, Jeroen W F van Dongen, Cesare Danesino, et al.
Pediatrics|November 20, 2025
Evaluation, Diagnosis, and Treatment of Sydenham Chorea: Consensus GuidelinesTerrence Thomas, Michael Eyre, Emanuela Ferrarin, et al.
Science (New York, N.Y.)|October 15, 2005
Sequence variants in SLITRK1 are associated with Tourette's syndromeJesse F Abelson, Kenneth Y Kwan, Brian J O'Roak, et al.
Human Molecular Genetics|June 2, 2019
De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypesLina Liang, Xia Li, Sébastien Moutton, et al.
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