Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Philip G, Murray"'
Autor:
Daphne Yau, Maria Salomon-Estebanez, Amish Chinoy, John Grainger, Ross J Craigie, Raja Padidela, Mars Skae, Mark J Dunne, Philip G Murray, Indraneel Banerjee
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2019)
Congenital hyperinsulinism (CHI) is an important cause of severe hypoglycaemia in infancy. To correct hypoglycaemia, high concentrations of dextrose are often required through a central venous catheter (CVC) with consequent risk of thrombosis. We des
Externí odkaz:
https://doaj.org/article/744d990cfc054927a853bbfd07b8635d
Publikováno v:
Parsons, S, Stevens, A, Whatmore, A, Clayton, P & Murray, P 2022, ' Role of ZBTB38 genotype and expression in growth and response to recombinant human growth hormone treatment ', Journal of the Endocrine Society, vol. 6, no. 3, bvac006 . https://doi.org/10.1210/jendso/bvac006
Context Single-nucleotide polymorphisms (SNPs) in ZBTB38 have been associated with idiopathic short stature (ISS) and adult height. Objective This study sought to (a) characterize the phenotype of ISS patients and their response to recombinant human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8e5ed060325a333e58f720719dea9b9
https://doi.org/10.1210/jendso/bvac006
https://doi.org/10.1210/jendso/bvac006
Publikováno v:
Journal of the Endocrine Society. 6(3)
Single-nucleotide polymorphisms (SNPs) inThis study sought to (a) characterize the phenotype of ISS patients and their response to recombinant human growth hormone (rhGH) byThe genotype-phenotype relationship of rs6764769 and rs724016 were explored i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f078b67ba35c0a2ba72deb433c66b1a
https://pubmed.ncbi.nlm.nih.gov/35178492
https://pubmed.ncbi.nlm.nih.gov/35178492
Autor:
Catherine Peters, Caroline Brain, Maria Guemes, Helen Spoudeas, Philip G Murray, Peter C. Hindmarsh, Mehul T. Dattani
Publikováno v:
European Journal of Pediatrics. 175:967-976
The diagnosis and management of paediatric Cushing syndrome (CS) is highly challenging. This study aims to characterise its presentation, diagnosis, management and outcome by a retrospective case review of 30 patients (14 females) followed at a singl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b29a461e3fbd8ca3ca9fcfdfb8dedfa
https://doi.org/10.1007/s00431-016-2727-5
https://doi.org/10.1007/s00431-016-2727-5
Autor:
Philip G, Murray, Peter E, Clayton
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical genetics. (2)
Human growth is a complex process starting at conception and completing in adolescence at the time of growth plate fusion. Growth can be divided into four phases: (1) fetal, where the predominant endocrine factors controlling growth are insulin and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03dc890355d976d9e5125efb6674ca0c
https://pubmed.ncbi.nlm.nih.gov/23613426
https://pubmed.ncbi.nlm.nih.gov/23613426
Autor:
Daniel Hanson, Philip G Murray, Tessa Coulson, Emma Saunders, Amit Sud, Andrew J Whatmore, Graeme C Black, Peter E Clayton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d8f5ec960c8d3b6ce33caeb0b48ef5a
https://doi.org/10.1210/endo-meetings.2011.part2.p19.p1-730
https://doi.org/10.1210/endo-meetings.2011.part2.p19.p1-730
