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Investigative Radiology|January 18, 2005
In vivo visualization of white matter fiber tracts of preterm- and term-infant brains with diffusion tensor magnetic resonance imagingSeung-Schik Yoo, Hae-Jeong Park, Janet S Soul, et al.Journal of Child Neurology|January 27, 2009
Cranial ultrasound lesions in the NICU predict cerebral palsy at age 2 years in children born at extremely low gestational ageKarl C K Kuban, Elizabeth N Allred, T Michael O'Shea, et al.Neurology. Genetics|October 27, 2021
Expanding the Phenotypic Spectrum of GPI Anchoring Deficiency Due to Biallelic Variants in GPAA1Alison M R Castle, Smrithi Salian, Haim Bassan, et al.Epilepsia|May 19, 2015
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcomeBronwyn E Grinton, Sarah E Heron, James T Pelekanos, et al.American Journal of Human Genetics|January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndromeSarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.Journal of Child Neurology|January 19, 2006
Video and CD-ROM as a training tool for performing neurologic examinations of 1-year-old children in a multicenter epidemiologic studyKarl C K Kuban, Michael O'Shea, Elizabeth Allred, et al.Annals of Neurology|June 10, 2020
SCN3A-Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain MalformationTariq Zaman, Katherine L Helbig, Jérôme Clatot, et al.American Journal of Medical Genetics. Part A|September 9, 2018
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literatureParisa Hemati, Anya Revah-Politi, Haim Bassan, et al.Brain : a Journal of Neurology|August 25, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implicationsKatrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.Pageof 6