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European Journal of Pediatrics|May 13, 2016
Management of Cushing syndrome in children and adolescents: experience of a single tertiary centreMaria Güemes, Philip G Murray, Caroline E Brain, et al.JCI Insight|December 8, 2025
A transcriptomic signature that predicts prehypertension in adolescence and higher systolic blood pressure in childhoodReena Perchard, Terence Garner, Philip G Murray, et al.Current Issues in Molecular Biology|February 27, 2026
Transcriptome and Metabolome Analyses Uncover Genes and Pathways Linking Growth Trajectories to Cardiometabolic Risk Markers in ChildhoodReena Perchard, Terence Garner, Lucy E Higgins, et al.Pediatric Research|April 9, 2016
Metabolites involved in glycolysis and amino acid metabolism are altered in short children born small for gestational agePhilip G Murray, Imogen Butcher, Warwick B Dunn, et al.Clinical Endocrinology|May 26, 2012
Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitinationPeter E Clayton, Dan Hanson, Lucia Magee, et al.American Journal of Human Genetics|June 2, 2009
The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1Dan Hanson, Philip G Murray, Amit Sud, et al.American 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.Journal of Medical Genetics|April 20, 2016
A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotypeCharlotte L Alston, Caoimhe Howard, Monika Oláhová, et al.The Journal of Clinical Endocrinology and Metabolism|August 16, 2016
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-SituAdeline K Nicholas, Eva G Serra, Hakan Cangul, et al.Nature Reviews. Endocrinology|September 3, 2016
Diagnosis and management of Silver-Russell syndrome: first international consensus statementEmma L Wakeling, Frédéric Brioude, Oluwakemi Lokulo-Sodipe, et al.Pageof 2