Dattani MT - Search Results

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: dattani mt. 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

2

What is a normal stimulated growth hormone concentration?

Dattani MT, Pringle PJ, Hindmarsh PC, Brook CG. Dattani MT, et al. J Endocrinol. 1992 Jun;133(3):447-50. doi: 10.1677/joe.0.1330447. J Endocrinol. 1992. PMID: 1613446

3

The measurement of growth hormone bioactivity in patient serum using an eluted stain assay.

Dattani MT, Hindmarsh PC, Pringle PJ, Brook CG, Marshall NJ. Dattani MT, et al. J Clin Endocrinol Metab. 1995 Sep;80(9):2675-83. doi: 10.1210/jcem.80.9.7545696. J Clin Endocrinol Metab. 1995. PMID: 7545696

4

Enhancement of growth hormone bioactivity by zinc in the eluted stain assay system.

Dattani MT, Hindmarsh PC, Brook CG, Robinson IC, Weir T, Marshall NJ. Dattani MT, et al. Endocrinology. 1993 Dec;133(6):2803-8. doi: 10.1210/endo.133.6.8243307. Endocrinology. 1993. PMID: 8243307

5

Acromegaly or chronic renal failure: a diagnostic dilemma.

Wong NA, Ahlquist JA, Camacho-Hübner C, Goodwin CJ, Dattani M, Marshall NJ, Wass JA. Wong NA, et al. Clin Endocrinol (Oxf). 1997 Feb;46(2):221-6. doi: 10.1046/j.1365-2265.1997.960911.x. Clin Endocrinol (Oxf). 1997. PMID: 9135706

6

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse.

Dattani MT, Martinez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Mårtensson IL, Toresson H, Fox M, Wales JK, Hindmarsh PC, Krauss S, Beddington RS, Robinson IC. Dattani MT, et al. Nat Genet. 1998 Jun;19(2):125-33. doi: 10.1038/477. Nat Genet. 1998. PMID: 9620767

7

HESX1: a novel gene implicated in a familial form of septo-optic dysplasia.

Dattani MT, Martinez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Wales JK, Hindmarsh PC, Beddington RS, Robinson IC. Dattani MT, et al. Acta Paediatr Suppl. 1999 Dec;88(433):49-54. doi: 10.1111/j.1651-2227.1999.tb14403.x. Acta Paediatr Suppl. 1999. PMID: 10626545 Review.

8

The molecular basis for developmental disorders of the pituitary gland in man.

Dattani MT, Robinson IC. Dattani MT, et al. Clin Genet. 2000 May;57(5):337-46. doi: 10.1034/j.1399-0004.2000.570503.x. Clin Genet. 2000. PMID: 10852367 Review.

9

Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.

Thomas PQ, Dattani MT, Brickman JM, McNay D, Warne G, Zacharin M, Cameron F, Hurst J, Woods K, Dunger D, Stanhope R, Forrest S, Robinson IC, Beddington RS. Thomas PQ, et al. Among authors: dattani mt. Hum Mol Genet. 2001 Jan 1;10(1):39-45. doi: 10.1093/hmg/10.1.39. Hum Mol Genet. 2001. PMID: 11136712

10

Two de novo mutations in the AR gene cause the complete androgen insensitivity syndrome in a pair of monozygotic twins.

Mongan NP, Jääskeläinen J, Green K, Schwabe JW, Shimura N, Dattani M, Hughes IA. Mongan NP, et al. J Clin Endocrinol Metab. 2002 Mar;87(3):1057-61. doi: 10.1210/jcem.87.3.8329. J Clin Endocrinol Metab. 2002. PMID: 11889162

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