Dev Med Child Neurol
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Publication Venue For
- Early intervention for very young children with or at high likelihood for autism spectrum disorder: An overview of reviews.. 64:1063-1076. 2022
- Motor function and safety after allogeneic cord blood and cord tissue-derived mesenchymal stromal cells in cerebral palsy: An open-label, randomized trial. 2022
- Diagnostic preferences include discussion of etiology for adults with cerebral palsy and their caregivers.. 64:723-733. 2022
- Neurosurgical procedures for children with myelomeningocele after fetal or postnatal surgery: a comparative effectiveness study.. 63:1294-1301. 2021
- Telehealth and wellness coaching: mirage or mainstay?. 63:631. 2021
- Stem cell therapies in cerebral palsy and autism spectrum disorder.. 63:503-510. 2021
- Social impairments in alternating hemiplegia of childhood.. 62:820-826. 2020
- Genetic variation in dopamine neurotransmission and motor development of infants born extremely-low-birthweight.. 62:750-757. 2020
- Parent preferences for neurodevelopmental screening in the neonatal intensive care unit.. 62:500-505. 2020
- Immunotherapy in selected patients with Down syndrome disintegrative disorder.. 61:847-851. 2019
- Cognitive, adaptive, and behavioral profiles and management of alternating hemiplegia of childhood.. 61:547-554. 2019
- Mycophenolate mofetil in the treatment of pediatric autoimmune central nervous system disease.. 61:388. 2019
- Motor function domains in alternating hemiplegia of childhood.. 59:822-828. 2017
- Can more urological deaths in spina bifida be prevented?. 57:594-595. 2015
- Callosal alterations in pyridoxine-dependent epilepsy.. 56:1106-1110. 2014
- Natural history of pyridoxine-dependent epilepsy: tools for prognostication.. 54:781-782. 2012
- Efficacy of the ketogenic diet in Lennox-Gastaut syndrome: a retrospective review of one institution's experience and summary of the literature.. 54:464-468. 2012
- Updates and future horizons on the understanding, diagnosis, and treatment of Sturge-Weber syndrome brain involvement.. 54:214-223. 2012
- Pyridoxine-dependent epilepsy and pyridoxine phosphate oxidase deficiency: unique clinical symptoms and non-specific EEG characteristics.. 52:602-603. 2010
- Neuromuscular hip dysplasia in Charcot-Marie-Tooth disease type 1A.. 51:408-411. 2009