Lu L - Search Results

1

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

2

[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.

3

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

4

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

5

New insights on hyperglycemia in 17-hydroxylase/17,20-lyase deficiency.

Xu L, Lu L, Tong A, Chen S, Li W, Zhang H, Ping F, Li Y. Xu L, et al. Among authors: lu l. Front Endocrinol (Lausanne). 2022 Jul 22;13:917420. doi: 10.3389/fendo.2022.917420. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35937831 Free PMC article.

6

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

7

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.

8

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.

9

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.

10

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

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