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Pediatric Dermatology|January 31, 2013
Clinical manifestations of pediatric psoriasis: results of a multicenter study in the United StatesKatherine Mercy, Mary Kwasny, Kelly M Cordoro, et al.European Journal of Pediatrics|July 1, 1996
Maternal non-phenylketonuric mild hyperphenylalaninemiaH L Levy, S E Waisbren, D Lobbregt, et al.American Journal of Human Genetics|July 1, 1995
A missense mutation (I278T) in the cystathionine beta-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotypeV E Shih, J M Fringer, R Mandell, et al.Journal of Diabetes Science and Technology|July 3, 2015
Sensitivity of the Predictive Hypoglycemia Minimizer System to the Algorithm Aggressiveness FactorDaniel A Finan, Eyal Dassau, Marc D Breton, et al.The Journal of Pediatrics|February 28, 2017
Psychological Factors May Play an Important Role in Pediatric Crohn's Disease Symptoms and DisabilityMiranda A L van Tilburg, Robyn Lewis Claar, Joan M Romano, et al.Primary Care Respiratory Journal : Journal of the General Practice Airways Group|May 29, 2007
The UK General Practice Airways Group (GPIAG): its formation, development, and influence on the management of asthma and other respiratory diseases over the last twenty yearsMark L Levy, Paul Stephenson, Peter Barritt, et al.Clinical Neurology and Neurosurgery|March 5, 2022
Maturation of the sella turcica and parasellar region: Surgical relevance for anterior skull base approaches in pediatric patientsRobert C Rennert, Michael G Brandel, Jeffrey A Steinberg, et al.Journal of Neurosurgery. Pediatrics|May 24, 2024
Examining barriers to care: a retrospective cohort analysis investigating the relationship between hospital volume and outcomes in pediatric patients with cerebral arteriovenous malformationsMichael G Brandel, Hernan Gonzalez, David D Gonda, et al.Plant Disease|February 21, 2019
First Report of Soybean Rust Caused by Phakopsora pachyrhizi in North CarolinaS R Koenning, A D Moore, T C Creswell, et al.American Journal of Human Genetics|March 21, 2000
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variationsM E Chamberlin, T Ubagai, S H Mudd, et al.Pageof 135