au.\*:("GALLENTINE, William B")
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Cytokine Storm of Acute Necrotizing EncephalopathyKANSAGRA, Sujay M; GALLENTINE, William B.Pediatric neurology. 2011, Vol 45, Num 6, pp 400-402, issn 0887-8994, 3 p.Article
Pediatric Neuro-Behçet's Disease Responsive to AdalimumabROBINSON, Angela Byun; GALLENTINE, William B; RABINOVICH, C. Egla et al.Pediatric neurology. 2010, Vol 43, Num 4, pp 291-293, issn 0887-8994, 3 p.Article
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association studyKASPERAVICIUTE, Dalia; CATARINO, Claudia B; SHIANNA, Kevin V et al.Brain. 2010, Vol 133, pp 2136-2147, issn 0006-8950, 12 p., 7Article
Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb AbnormalitiesBALLIF, Blake C; THEISEN, Aaron; SHANE, Kate et al.American journal of human genetics. 2010, Vol 86, Num 3, pp 454-461, issn 0002-9297, 8 p.Article
Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy SyndromesHEINZEN, Erin L; RADTKE, Rodney A; DUNCAN, John S et al.American journal of human genetics. 2010, Vol 86, Num 5, pp 707-718, issn 0002-9297, 12 p.Article
Electrographic seizures in pediatric ICU patients: Cohort study of risk factors and mortalityABEND, Nicholas S; ARNDT, Daniel H; LODDENKEMPER, Tobias et al.Neurology. 2013, Vol 81, Num 4, pp 383-391, issn 0028-3878, 9 p.Article
Exome Sequencing Followed by Large-Scale Genotyping Fails to Identify Single Rare Variants of Large Effect in Idiopathic Generalized EpilepsyHEINZEN, Erin L; DEPONDT, Chantal; CRONIN, Kenneth D et al.American journal of human genetics. 2012, Vol 91, Num 2, pp 293-302, issn 0002-9297, 10 p.Article