Dattani MT - Search Results

1

Cushing syndrome in a child due to pro-opiomelanocortin (POMC) secretion from a yolk sac tumor.

Gevers EF, Meredith S, Shah P, Torpiano J, Peters C, Sebire NJ, Slater O, White A, Dattani MT. Gevers EF, et al. Among authors: dattani mt. Eur J Endocrinol. 2017 Feb;176(2):K1-K7. doi: 10.1530/EJE-16-0776. Epub 2016 Nov 22. Eur J Endocrinol. 2017. PMID: 27879325 Free article.

2

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

3

Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal function.

Lin L, Philibert P, Ferraz-de-Souza B, Kelberman D, Homfray T, Albanese A, Molini V, Sebire NJ, Einaudi S, Conway GS, Hughes IA, Jameson JL, Sultan C, Dattani MT, Achermann JC. Lin L, et al. Among authors: dattani mt. J Clin Endocrinol Metab. 2007 Mar;92(3):991-9. doi: 10.1210/jc.2006-1672. Epub 2007 Jan 2. J Clin Endocrinol Metab. 2007. PMID: 17200175 Free PMC article.

4

Acanthosis nigricans and insulin sensitivity in patients with achondroplasia and hypochodroplasia due to FGFR3 mutations.

Alatzoglou KS, Hindmarsh PC, Brain C, Torpiano J, Dattani MT. Alatzoglou KS, et al. Among authors: dattani mt. J Clin Endocrinol Metab. 2009 Oct;94(10):3959-63. doi: 10.1210/jc.2009-0322. Epub 2009 Jul 21. J Clin Endocrinol Metab. 2009. PMID: 19622626

5

Use of combined liothyronine and thyroxine therapy for consumptive hypothyroidism associated with hepatic haemangiomas in infancy.

Peters C, Langham S, Mullis PE, Dattani MT. Peters C, et al. Among authors: dattani mt. Horm Res Paediatr. 2010;74(2):149-52. doi: 10.1159/000281884. Epub 2010 Jun 3. Horm Res Paediatr. 2010. PMID: 20516650 Free article.

6

How to use insulin-like growth factor 1 (IGF1).

Peters CJ, Dattani MT. Peters CJ, et al. Among authors: dattani mt. Arch Dis Child Educ Pract Ed. 2012 Jun;97(3):114-8. doi: 10.1136/archdischild-2011-300265. Epub 2012 Jan 20. Arch Dis Child Educ Pract Ed. 2012. PMID: 22267103

7

An infant with pseudohyperkalemia, hemolysis, and seizures: cation-leaky GLUT1-deficiency syndrome due to a SLC2A1 mutation.

Bawazir WM, Gevers EF, Flatt JF, Ang AL, Jacobs B, Oren C, Grunewald S, Dattani M, Bruce LJ, Stewart GW. Bawazir WM, et al. J Clin Endocrinol Metab. 2012 Jun;97(6):E987-93. doi: 10.1210/jc.2012-1399. Epub 2012 Apr 6. J Clin Endocrinol Metab. 2012. PMID: 22492876

8

Deconvolution analysis of 24-h serum cortisol profiles informs the amount and distribution of hydrocortisone replacement therapy.

Peters CJ, Hill N, Dattani MT, Charmandari E, Matthews DR, Hindmarsh PC. Peters CJ, et al. Among authors: dattani mt. Clin Endocrinol (Oxf). 2013 Mar;78(3):347-51. doi: 10.1111/j.1365-2265.2012.04502.x. Clin Endocrinol (Oxf). 2013. PMID: 22803584

9

Structural pituitary abnormalities associated with CHARGE syndrome.

Gregory LC, Gevers EF, Baker J, Kasia T, Chong K, Josifova DJ, Caimari M, Bilan F, McCabe MJ, Dattani MT. Gregory LC, et al. Among authors: dattani mt. J Clin Endocrinol Metab. 2013 Apr;98(4):E737-43. doi: 10.1210/jc.2012-3467. Epub 2013 Mar 22. J Clin Endocrinol Metab. 2013. PMID: 23526466 Free PMC article.

10

Cardiovascular risk factors in children and adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Subbarayan A, Dattani MT, Peters CJ, Hindmarsh PC. Subbarayan A, et al. Among authors: dattani mt. Clin Endocrinol (Oxf). 2014 Apr;80(4):471-7. doi: 10.1111/cen.12265. Epub 2013 Jul 8. Clin Endocrinol (Oxf). 2014. PMID: 23751160 Free PMC article.

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