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George Hoganson

Showing results (1-10 of 18) with videos related to

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Molecular Genetics & Genomic Medicine|August 7, 2015
Behavioral abnormalities are common and severe in patients with distal 22q11.2 microdeletions and microduplicationsValerie Lindgren, Anne McRae, Richard Dineen, et al.
Pediatric Neurology|January 7, 2015
Internal carotid artery dissection after a roller coaster ride in a 4-year-old: case report and review of the literatureAmre Nouh, Daniel Vela-Duarte, Thomas Grobelny, et al.
Journal of the American Academy of Dermatology|January 17, 2004
Infantile systemic hyalinosisHelen T Shin, Amy Paller, George Hoganson, et al.
JAMA Pediatrics|October 2, 2023
Multisite Oral Amoxicillin Challenges During Pediatric Emergency Department VisitsDavid Vyles, George Hoganson, Constance McAneney, et al.
Journal of the International Neuropsychological Society : JINS|October 8, 2005
Early and late life cognitive activity and cognitive systems in old ageRobert S Wilson, Lisa L Barnes, Kristin R Krueger, et al.
Neuroepidemiology|April 28, 2005
Early life socioeconomic status and late life risk of Alzheimer's diseaseRobert S Wilson, Paul A Scherr, George Hoganson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 28, 2020
Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDGPeter Witters, Shawn Tahata, Rita Barone, et al.
Journal of Human Genetics|December 28, 2017
Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndromeMaria Helgeson, Jennifer Keller-Ramey, Amy Knight Johnson, et al.
American Journal of Human Genetics|February 13, 2018
Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris SyndromeGeorgia Vasileiou, Silvia Vergarajauregui, Sabine Endele, et al.
Brain : a Journal of Neurology|October 6, 2022
Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defectsLama AlAbdi, Muriel Desbois, Domniţa-Valeria Rusnac, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Molecular Genetics & Genomic Medicine|August 7, 2015
Behavioral abnormalities are common and severe in patients with distal 22q11.2 microdeletions and microduplicationsValerie Lindgren, Anne McRae, Richard Dineen, et al.
Pediatric Neurology|January 7, 2015
Internal carotid artery dissection after a roller coaster ride in a 4-year-old: case report and review of the literatureAmre Nouh, Daniel Vela-Duarte, Thomas Grobelny, et al.
Journal of the American Academy of Dermatology|January 17, 2004
Infantile systemic hyalinosisHelen T Shin, Amy Paller, George Hoganson, et al.
JAMA Pediatrics|October 2, 2023
Multisite Oral Amoxicillin Challenges During Pediatric Emergency Department VisitsDavid Vyles, George Hoganson, Constance McAneney, et al.
Journal of the International Neuropsychological Society : JINS|October 8, 2005
Early and late life cognitive activity and cognitive systems in old ageRobert S Wilson, Lisa L Barnes, Kristin R Krueger, et al.
Neuroepidemiology|April 28, 2005
Early life socioeconomic status and late life risk of Alzheimer's diseaseRobert S Wilson, Paul A Scherr, George Hoganson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 28, 2020
Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDGPeter Witters, Shawn Tahata, Rita Barone, et al.
Journal of Human Genetics|December 28, 2017
Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndromeMaria Helgeson, Jennifer Keller-Ramey, Amy Knight Johnson, et al.
American Journal of Human Genetics|February 13, 2018
Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris SyndromeGeorgia Vasileiou, Silvia Vergarajauregui, Sabine Endele, et al.
Brain : a Journal of Neurology|October 6, 2022
Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defectsLama AlAbdi, Muriel Desbois, Domniţa-Valeria Rusnac, et al.
Pageof 2