Nie M - Search Results

1

[Clinical characteristics of testicular adrenal rest tumor and factors associated with its occurrence in 21-hydroxylase deficiency patients].

Gao YJ, Yu BQ, Lu L, Wu XY, Mao JF, Wang X, Tong AL, Chen S, Nie M. Gao YJ, et al. Among authors: nie m. Zhonghua Yi Xue Za Zhi. 2020 Jun 23;100(24):1850-1855. doi: 10.3760/cma.j.cn112137-20191104-02389. Zhonghua Yi Xue Za Zhi. 2020. PMID: 32575926 Chinese.

2

Novel human pathological mutations. Gene symbol: NR0B1. Disease: adrenal hypoplasia.

Nie M, Fu Y, Lu L, Mao J, Chen Z, Zhang K, Xia W, Xing X, Sun M, Lu Z. Nie M, et al. Hum Genet. 2009 Apr;125(3):347. Hum Genet. 2009. PMID: 19320028 No abstract available.

3

Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasia.

Nie M, Fu Y, Lu L, Pan H, Mao J, Chen Z, Zhang K, Xia W, Xing X, Meili S, Lu Z. Nie M, et al. Hum Genet. 2009 Apr;125(3):348. Hum Genet. 2009. PMID: 19320031 No abstract available.

4

Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasia.

Nie M, Fu Y, Lu L, Pan H, Mao J, Chen Z, Zhang K, Xia W, Xing X, Meili S, Lu Z. Nie M, et al. Hum Genet. 2009 Apr;125(3):348. Hum Genet. 2009. PMID: 19320032 No abstract available.

5

Heteroplasmy level of the mitochondrial tRNaLeu(UUR) A3243G mutation in a Chinese family is positively associated with earlier age-of-onset and increasing severity of diabetes.

Zhang S, Tong AL, Zhang Y, Nie M, Li YX, Wang H. Zhang S, et al. Among authors: nie m. Chin Med Sci J. 2009 Mar;24(1):20-5. doi: 10.1016/s1001-9294(09)60053-5. Chin Med Sci J. 2009. PMID: 19382419

6

Mutational analysis of androgen receptor gene in four Chinese patients with male pseudohermaphroditism.

Wu X, Zhou Q, Mao J, Lu S, Nie M. Wu X, et al. Among authors: nie m. Fertil Steril. 2010 Apr;93(6):2076.e1-4. doi: 10.1016/j.fertnstert.2009.11.025. Epub 2010 Jan 8. Fertil Steril. 2010. PMID: 20056211 Free article.

7

Adult-onset idiopathic hypogonadotropic hypogonadism: possible aetiology, clinical manifestations and management.

Mao JF, Nie M, Lu SY, Wu XY. Mao JF, et al. Among authors: nie m. Asian J Androl. 2010 Jul;12(4):611-4. doi: 10.1038/aja.2010.34. Epub 2010 Jun 7. Asian J Androl. 2010. PMID: 20531282 Free PMC article. No abstract available.

8

Five novel mutations of SRD5A2 found in eight Chinese patients with 46,XY disorders of sex development.

Nie M, Zhou Q, Mao J, Lu S, Wu X. Nie M, et al. Mol Hum Reprod. 2011 Jan;17(1):57-62. doi: 10.1093/molehr/gaq072. Epub 2010 Aug 24. Mol Hum Reprod. 2011. PMID: 20736251

9

[Clinical and molecular genetic analyses for a sporadic parathyroid carcinoma].

Wang CY, Wang O, Nie M, Zhao DC, Xia WB, Li M, Guan H, Meng XW, Xing XP. Wang CY, et al. Among authors: nie m. Zhonghua Yi Xue Za Zhi. 2010 Jun 22;90(24):1694-7. Zhonghua Yi Xue Za Zhi. 2010. PMID: 20979880 Chinese.

10

[Clinical features of 9 patients with X-linked adrenal hypoplasia congenita caused by DAX1/NR0B1 gene mutations].

Fu Y, Nie M, Xia WB, Lu L, Mao JF, Pan H, Wu XY, Zhao WG. Fu Y, et al. Among authors: nie m. Zhonghua Yi Xue Za Zhi. 2010 Aug 10;90(30):2119-22. Zhonghua Yi Xue Za Zhi. 2010. PMID: 21029627 Chinese.

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