Zobrazeno 1 - 10
of 239
pro vyhledávání: '"J. O. Turner"'
Autor:
Turner, J. J. O.1,2 jeremy.turner@nnuh.nhs.uk, Foxwell, K. M.1, Kanji, R.1, Brenner, C.1, Wood, S.3, Foxwell, B. M. J.1, Feldmann, M.1
Publikováno v:
Clinical & Experimental Immunology. Dec2010, Vol. 162 Issue 3, p487-493. 7p. 1 Black and White Photograph, 3 Graphs.
Publikováno v:
Clinical Endocrinology. 97:562-567
Individuals with chronic hypoparathyroidism may experience suboptimal medical care with high frequency of unplanned hospitalisation and iatrogenic harm. In 2015 the European Society for Endocrinology published consensus guidelines on the management o
Autor:
Jian Shen Kiam, Jeremy J O Turner
Publikováno v:
Medicine. 49:558-561
Autor:
Jeremy J O Turner
Publikováno v:
Medicine. 45:551-554
Publikováno v:
Journal of cell science. 131(22)
White adipocytes are key regulators of metabolic homeostasis, which release stored energy as free fatty acids via lipolysis. Adipocytes possess both basal and stimulated lipolytic capacity, but limited information exists regarding the molecular mecha
Autor:
Kaplová, E.1 namornice@centrum.cz
Publikováno v:
Czech Dental Journal / Ceská Stomatologie a Praktické Zubni Lékarstvi. 2014, Vol. 114 Issue 1, p3-8. 6p.
Autor:
A A J, Pannett, A M, Kennedy, J J O, Turner, S A, Forbes, B M, Cavaco, J H D, Bassett, L, Cianferotti, B, Harding, B, Shine, F, Flinter, C G H, Maidment, R, Trembath, R V, Thakker
Publikováno v:
Clinical endocrinology. 58(5)
Familial isolated hyperparathyroidism (FIHP) is an autosomal dominant disorder characterized by uniglandular or multiglandular parathyroid tumours that occur in the absence of other endocrine tumours. The disorder may represent either an early stage
Publikováno v:
Clinical endocrinology. 57(6)
Preoperative localisation is important for successful surgical treatment of gastrinomas. However, a satisfactory method that achieves this has not been defined, and at present somatostatin receptor scintigraphy and selective intra-arterial stimulatio
Autor:
Jeremy J. O. Turner, Poloko D. Leotlela, Anna A. J. Pannett, Simon A. Forbes, J. H. Duncan Bassett, Brian Harding, Paul T. Christie, David Bowen-Jones, Sian Ellard, Andrew Hattersley, Charles E. Jackson, Richard Pope, Oliver W. Quarrell, Richard Trembath, Rajesh V. Thakker
Publikováno v:
The Journal of clinical endocrinology and metabolism. 87(6)
MEN1 is an autosomal dominant disorder characterized by parathyroid, pituitary, and pancreatic tumors. The MEN1 gene is located on chromosome 11q13 and encodes a 610-amino acid protein. MEN1 mutations are of diverse types and are scattered throughout
Publikováno v:
Frontiers in Pharmacology; 2024, p1-12, 12p