Showing results (21-30 of 88) with videos related to
Sort By:
Pageof 9
JRSM Open|November 30, 2016
Assessing the population impact of low rates of vitamin D supplementation on type 1 diabetes using a new statistical methodChristos S Zipitis, Zulf M Mughal, Peter E ClaytonJournal of Pediatric Endocrinology & Metabolism : JPEM|June 1, 2005
Maternal age in patients with septo-optic dysplasiaPhilip G Murray, Wendy F Paterson, Malcolm D C DonaldsonAmerican Journal of Human Genetics|July 9, 2011
Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growthDan Hanson, Philip G Murray, James O'Sullivan, et al.Clinical Endocrinology|September 27, 2012
The challenge of delivering endocrine care and successful transition to adult services in adolescents with congenital adrenal hyperplasia: experience in a single centre over 18 yearsHelena Gleeson, Joanne Davis, Julie Jones, et al.Pediatric Endocrinology Reviews : PER|May 14, 2010
Diagnosis and management of primary insulin-like growth factor-I deficiency: current perspectives and clinical updatePhilippe Backeljauw, Peter Bang, Peter E Clayton, et al.Archives of Disease in Childhood|November 15, 2013
No evidence of an increase in early infant mortality from congenital adrenal hyperplasia in the absence of screeningBeverly E Hird, Lesley Tetlow, Simon Tobi, et al.Hormone Research|October 29, 2002
European audit of current practice in diagnosis and treatment of childhood growth hormone deficiencyAnders Juul, Sergio Bernasconi, Peter E Clayton, et al.Hypertension (Dallas, Tex. : 1979)|October 16, 2013
The impact of malaria in pregnancy on changes in blood pressure in children during their first year of lifeOmolola O Ayoola, Olayemi O Omotade, Isla Gemmell, et al.The Journal of Pediatrics|January 21, 2006
Geographical distribution of optic nerve hypoplasia and septo-optic dysplasia in Northwest EnglandLeena Patel, Richard J Q McNally, Elizabeth Harrison, et al.Pediatric Research|March 25, 2011
Reduced pericellular sensitivity to IGF-I in fibroblasts from girls with Turner syndrome: a mechanism to impair clinical responses to GHMelissa Westwood, Shahin H Tajbakhsh, Kirk W Siddals, et al.Pageof 9