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Current Opinion in Pediatrics|May 26, 2011
The interplay of infection and genetics in acute necrotizing encephalopathyDerek E NeilsonAmerican Journal of Medical Genetics. Part A|May 14, 2011
Familial 9q22.3 microduplication spanning PTCH1 causes short stature syndrome with mild intellectual disability and dysmorphic featuresKosuke Izumi, Amanda Hahn, Laurie Christ, et al.Developmental Medicine and Child Neurology|October 9, 2009
Recurrent acute necrotizing encephalopathy following influenza A in a genetically predisposed familyArtemis D Gika, Philip Rich, Sachin Gupta, et al.Pediatrics|February 10, 2010
Acute necrotizing encephalopathy in 3 brothersElysa J Marco, Jane E Anderson, Derek E Neilson, et al.American Journal of Medical Genetics|March 29, 2002
Mixed clefting type in Rapp-Hodgkin syndromeDerek E Neilson, Jeanne W Brunger, Shauna Heeger, et al.Pediatric Radiology|October 15, 2020
Fetal brain small vessel disease 1 caused by a novel mutation in the COL4A1 geneElizabeth C England, Patricia Cornejo, Derek E Neilson, et al.Human Molecular Genetics|October 9, 2014
Activating PIK3CA alleles and lymphangiogenic phenotype of lymphatic endothelial cells isolated from lymphatic malformationsAlexander J Osborn, Peter Dickie, Derek E Neilson, et al.The Journal of Clinical Endocrinology and Metabolism|June 1, 2019
Central Diabetes Insipidus in a Patient With NFKB2 Mutation: Expanding the Endocrine Phenotype in DAVID SyndromeNat Nasomyont, Andrew W Lindsley, Amal Assa'ad, et al.Annals of Neurology|February 3, 2004
Autosomal dominant acute necrotizing encephalopathy maps to 2q12.1-2q13Derek E Neilson, Heidi S Feiler, Kirk C Wilhelmsen, et al.Journal of Child Neurology|April 12, 2015
The Clinical Utility of a Single-Nucleotide Polymorphism Microarray in Patients With Epilepsy at a Tertiary Medical CenterSarah A Hrabik, Shannon M Standridge, Hansel M Greiner, et al.Pageof 2