Yau M - Search Results

1

A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred.

Yau M, Azkawi HS, Haider S, Khattab A, Badi MA, Abdullah W, Senani AA, Wilson RC, Yuen T, Zaidi M, New MI. Yau M, et al. Ann N Y Acad Sci. 2016 Jul;1376(1):65-71. doi: 10.1111/nyas.13162. Epub 2016 Aug 15. Ann N Y Acad Sci. 2016. PMID: 27526338

2

Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma.

New MI, Tong YK, Yuen T, Jiang P, Pina C, Chan KC, Khattab A, Liao GJ, Yau M, Kim SM, Chiu RW, Sun L, Zaidi M, Lo YM. New MI, et al. Among authors: yau m. J Clin Endocrinol Metab. 2014 Jun;99(6):E1022-30. doi: 10.1210/jc.2014-1118. Epub 2014 Feb 28. J Clin Endocrinol Metab. 2014. PMID: 24606108 Free PMC article.

3

Ovarian carcinoma in a 14-year-old with classical salt-wasting congenital adrenal hyperplasia and bilateral adrenalectomy.

Pina C, Khattab A, Katzman P, Bruckner L, Andolina J, New M, Yau M. Pina C, et al. Among authors: yau m. J Pediatr Endocrinol Metab. 2015 May;28(5-6):663-7. doi: 10.1515/jpem-2014-0299. J Pediatr Endocrinol Metab. 2015. PMID: 25427061

4

Pitfalls in hormonal diagnosis of 17-beta hydroxysteroid dehydrogenase III deficiency.

Khattab A, Yuen T, Yau M, Domenice S, Frade Costa EM, Diya K, Muhuri D, Pina CE, Nishi MY, Yang AC, de Mendonça BB, New MI. Khattab A, et al. Among authors: yau m. J Pediatr Endocrinol Metab. 2015 May;28(5-6):623-8. doi: 10.1515/jpem-2014-0295. J Pediatr Endocrinol Metab. 2015. PMID: 25536660

5

A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordance.

Khattab A, Yuen T, Al-Malki S, Yau M, Kazmi D, Sun L, Harbison M, Haider S, Zaidi M, New MI. Khattab A, et al. Among authors: yau m. Ann N Y Acad Sci. 2016 Jan;1364(1):5-10. doi: 10.1111/nyas.12864. Epub 2015 Aug 20. Ann N Y Acad Sci. 2016. PMID: 26291314 Free PMC article.

6

Noninvasive Prenatal Diagnosis of Congenital Adrenal Hyperplasia.

Khattab A, Yuen T, Sun L, Yau M, Barhan A, Zaidi M, Lo YM, New MI. Khattab A, et al. Among authors: yau m. Endocr Dev. 2016;30:37-41. doi: 10.1159/000439326. Epub 2015 Dec 10. Endocr Dev. 2016. PMID: 26683339 Review.

7

Apparent mineralocorticoid excess and the long term treatment of genetic hypertension.

Razzaghy-Azar M, Yau M, Khattab A, New MI. Razzaghy-Azar M, et al. Among authors: yau m. J Steroid Biochem Mol Biol. 2017 Jan;165(Pt A):145-150. doi: 10.1016/j.jsbmb.2016.02.014. Epub 2016 Feb 15. J Steroid Biochem Mol Biol. 2017. PMID: 26892095

8

Congenital Adrenal Hyperplasia: Unresolved Issues.

Yau M, Khattab A, Poppas D, Ghizzoni L, New M. Yau M, et al. Front Horm Res. 2016;46:184-95. doi: 10.1159/000443919. Epub 2016 May 17. Front Horm Res. 2016. PMID: 27211889 Review.

9

Prenatal Diagnosis of Congenital Adrenal Hyperplasia.

Yau M, Khattab A, New MI. Yau M, et al. Endocrinol Metab Clin North Am. 2016 Jun;45(2):267-81. doi: 10.1016/j.ecl.2016.01.001. Epub 2016 Mar 31. Endocrinol Metab Clin North Am. 2016. PMID: 27241964 Review.

10

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.

Yau M, Haider S, Khattab A, Ling C, Mathew M, Zaidi S, Bloch M, Patel M, Ewert S, Abdullah W, Toygar A, Mudryi V, Al Badi M, Alzubdi M, Wilson RC, Al Azkawi HS, Ozdemir HN, Abu-Amer W, Hertecant J, Razzaghy-Azar M, Funder JW, Al Senani A, Sun L, Kim SM, Yuen T, Zaidi M, New MI. Yau M, et al. Proc Natl Acad Sci U S A. 2017 Dec 26;114(52):E11248-E11256. doi: 10.1073/pnas.1716621115. Epub 2017 Dec 11. Proc Natl Acad Sci U S A. 2017. PMID: 29229831 Free PMC article.

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