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Pediatric Dermatology|March 18, 2015
Improving the Dermatologic Care of Individuals with Autism: A Review of Relevant Issues and a PerspectiveVikash S Oza, Elysa Marco, Ilona J FriedenArchives of Neurology|August 8, 2002
Predictive model for pain recurrence after posterior fossa surgery for trigeminal neuralgiaPhilip V Theodosopoulos, Elysa Marco, Carol Applebury, et al.Neuropsychology|December 22, 2014
Individuals with agenesis of the corpus callosum show sensory processing differences as measured by the sensory profileCarly Demopoulos, Monica S Arroyo, Winnie Dunn, et al.Clinical Dysmorphology|March 17, 2005
Case report: Y;6 translocation with deletion of 6pOphir D Klein, Kendall Backstrand, Philip D Cotter, et al.Annals of Neurology|June 9, 2007
Congenital lymphocytic choriomeningitis virus infection: spectrum of diseaseDaniel J Bonthius, Rhonda Wright, Brian Tseng, et al.Pediatric Neurology|February 26, 2005
Infant botulism, type F, presenting at 54 hours of lifeCorinne A Keet, Christine K Fox, Marta Margeta, et al.American Journal of Medical Genetics. Part A|January 13, 2021
Expansion of NEUROD2 phenotypes to include developmental delay without seizuresEmily K Mis, Annalisa G Sega, Rebecca H Signer, et al.Neurology. Genetics|June 8, 2017
ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlationMichael Alber, Vera M Kalscheuer, Elysa Marco, et al.American Journal of Human Genetics|June 15, 2007
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disordersFrancesco Brancati, Giuseppe Barrano, Jennifer L Silhavy, et al.Journal of Medical Genetics|March 11, 2020
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHDJorge Luis Granadillo, Alexander P A Stegmann, Hui Guo, et al.Pageof 2