Lu L - Search Results

1

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. Among authors: lu z, lu l. Hum Genet. 2009 Apr;125(3):348. Hum Genet. 2009. PMID: 19320031 No abstract available.

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. Among authors: lu z, lu l. 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. Among authors: lu z, lu l. Hum Genet. 2009 Apr;125(3):348. Hum Genet. 2009. PMID: 19320032 No abstract available.

4

[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: lu l. Zhonghua Yi Xue Za Zhi. 2010 Aug 10;90(30):2119-22. Zhonghua Yi Xue Za Zhi. 2010. PMID: 21029627 Chinese.

5

The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency.

Gao Y, Lu L, Yu B, Mao J, Wang X, Nie M, Wu X. Gao Y, et al. Among authors: lu l. J Clin Endocrinol Metab. 2020 Jul 1;105(7):dgaa199. doi: 10.1210/clinem/dgaa199. J Clin Endocrinol Metab. 2020. PMID: 32291442

6

High incidence of hypertension-mediated organ damage in a series of Chinese patients with 17α-hydroxylase deficiency.

Zhao Z, Lu L, Wang O, Wu X, Sun B, Zhang W, Wang X, Mao J, Chen S, Tong A, Nie M. Zhao Z, et al. Among authors: lu l. Endocrine. 2022 Apr;76(1):151-161. doi: 10.1007/s12020-021-02966-w. Epub 2022 Jan 14. Endocrine. 2022. PMID: 35032013

7

High prevalence of hypertension and target organ damage in patients with 11β-hydroxylase deficiency.

Sun B, Lu L, Gao Y, Yu B, Chen S, Tong A, Wu X, Mao J, Wang X, Zhao Z, Zhang W, Nie M. Sun B, et al. Among authors: lu l. Clin Endocrinol (Oxf). 2022 May;96(5):657-665. doi: 10.1111/cen.14677. Epub 2022 Feb 3. Clin Endocrinol (Oxf). 2022. PMID: 35067946

8

A noninvasive scoring model for the differential diagnosis of ACTH-dependent Cushing's syndrome: a retrospective analysis of 311 patients based on easy-to-use parameters.

Lyu X, Zhang D, Pan H, Zhu H, Chen S, Lu L. Lyu X, et al. Among authors: lu l. Endocrine. 2022 Oct;78(1):114-122. doi: 10.1007/s12020-022-03081-0. Epub 2022 Aug 4. Endocrine. 2022. PMID: 35925471

9

Pituicytoma Associated with Suspected Cushing's Disease: Two Case Reports and a Literature Review.

Xiao T, Duan L, Chen S, Lu L, Yao Y, Mao X, Zhu H, Pan H. Xiao T, et al. Among authors: lu l. J Clin Med. 2022 Aug 17;11(16):4805. doi: 10.3390/jcm11164805. J Clin Med. 2022. PMID: 36013043 Free PMC article.

10

The clinical and metabolic characteristics of children and adolescents with hypothalamic dysfunction: A single-centre study from China.

Ke X, Yuan X, Zhang Y, Wang L, Feng F, Yao Y, You H, Yang H, Lu L, Chen S, Duan L, Gong F, Pan H, Zhu H. Ke X, et al. Among authors: lu l. Clin Endocrinol (Oxf). 2023 Jan;98(1):59-67. doi: 10.1111/cen.14814. Epub 2022 Sep 5. Clin Endocrinol (Oxf). 2023. PMID: 35978545

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