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Page 1
Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency.
Turton JP, Reynaud R, Mehta A, Torpiano J, Saveanu A, Woods KS, Tiulpakov A, Zdravkovic V, Hamilton J, Attard-Montalto S, Parascandalo R, Vella C, Clayton PE, Shalet S, Barton J, Brue T, Dattani MT. Turton JP, et al. Among authors: shalet s. J Clin Endocrinol Metab. 2005 Aug;90(8):4762-70. doi: 10.1210/jc.2005-0570. Epub 2005 May 31. J Clin Endocrinol Metab. 2005. PMID: 15928241
HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.
McNay DE, Turton JP, Kelberman D, Woods KS, Brauner R, Papadimitriou A, Keller E, Keller A, Haufs N, Krude H, Shalet SM, Dattani MT. McNay DE, et al. Among authors: shalet sm. J Clin Endocrinol Metab. 2007 Feb;92(2):691-7. doi: 10.1210/jc.2006-1609. Epub 2006 Dec 5. J Clin Endocrinol Metab. 2007. PMID: 17148560
Cranial irradiation and early puberty.
Ogilvy-Stuart AL, Clayton PE, Shalet SM. Ogilvy-Stuart AL, et al. Among authors: shalet sm. J Clin Endocrinol Metab. 1994 Jun;78(6):1282-6. doi: 10.1210/jcem.78.6.8200926. J Clin Endocrinol Metab. 1994. PMID: 8200926
Biochemical tests in the diagnosis of childhood growth hormone deficiency.
Tillmann V, Buckler JM, Kibirige MS, Price DA, Shalet SM, Wales JK, Addison MG, Gill MS, Whatmore AJ, Clayton PE. Tillmann V, et al. Among authors: shalet sm. J Clin Endocrinol Metab. 1997 Feb;82(2):531-5. doi: 10.1210/jcem.82.2.3750. J Clin Endocrinol Metab. 1997. PMID: 9024249
The acute leptin response to GH.
Lissett CA, Clayton PE, Shalet SM. Lissett CA, et al. Among authors: shalet sm. J Clin Endocrinol Metab. 2001 Sep;86(9):4412-5. doi: 10.1210/jcem.86.9.7796. J Clin Endocrinol Metab. 2001. PMID: 11549684 Clinical Trial.
461 results