Kaichuang Zhang - Search Results

Year	Number of Results
2017	4
2018	1
2022	4
2023	6
2024	1

1

Genetic and phenotypic spectrum of non-21-hydroxylase-deficiency primary adrenal insufficiency in childhood: data from 111 Chinese patients.

Duan Y, Zheng W, Xia Y, Zhang H, Liang L, Wang R, Yang Y, Zhang K, Lu D, Sun Y, Han L, Yu Y, Gu X, Sun Y, Xiao B, Qiu W. Duan Y, et al. Among authors: zhang k. J Med Genet. 2023 Dec 21;61(1):27-35. doi: 10.1136/jmg-2022-108952. J Med Genet. 2023. PMID: 37586839

2

Ignition and Combustion Characteristic of B·Mg Alloy Powders.

Ma Y, Zhang K, Ma S, He J, Gai X, Zhang X. Ma Y, et al. Among authors: zhang k. Materials (Basel). 2022 Apr 7;15(8):2717. doi: 10.3390/ma15082717. Materials (Basel). 2022. PMID: 35454411 Free PMC article.

3

Clinical and genetic characteristics of 42 Chinese paediatric patients with X-linked adrenal hypoplasia congenita.

Zheng W, Duan Y, Xia Y, Liang L, Gong Z, Wang R, Lu D, Zhang K, Yang Y, Sun Y, Zhang H, Han L, Gong Z, Xiao B, Qiu W. Zheng W, et al. Among authors: zhang k. Orphanet J Rare Dis. 2023 May 26;18(1):126. doi: 10.1186/s13023-023-02737-y. Orphanet J Rare Dis. 2023. PMID: 37237297 Free PMC article.

4

[Analysis of NF2 gene mutations in intraspinal Schwannomas].

Liu S, Chen S, Zhang K, Lin J, Yang Q, Zhang Y, Liu S, Liu S. Liu S, et al. Among authors: zhang k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):637-641. doi: 10.3760/cma.j.issn.1003-9406.2017.05.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981922 Chinese.

5

Clinical profile, genetic spectrum and therapy evaluation of 19 Chinese pediatric patients with lipoprotein lipase deficiency.

Xia Y, Zheng W, Du T, Gong Z, Liang L, Wang R, Yang Y, Zhang K, Lu D, Chen X, Sun Y, Sun Y, Xiao B, Qiu W. Xia Y, et al. Among authors: zhang k. J Clin Lipidol. 2023 Nov-Dec;17(6):808-817. doi: 10.1016/j.jacl.2023.09.012. Epub 2023 Sep 27. J Clin Lipidol. 2023. PMID: 37858495

6

[Analysis of disease spectrum for abnormal 3-hydroxyisovalerylcarnitine metabolism identified through newborn screening and clinical diagnosis].

Yang Y, Qiu W, Zhang H, Liang L, Lu D, Zhang K, Chen T, Xu F, Gu X, Han L. Yang Y, et al. Among authors: zhang k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Dec 10;40(12):1466-1471. doi: 10.3760/cma.j.cn511374-20220916-00626. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37994125 Chinese.

7

Clinical, biochemical, and molecular genetic characteristics of patients with primary carnitine deficiency identified by newborn screening in Shanghai, China.

Chang S, Yang Y, Xu F, Ji W, Zhan X, Gao X, Chen T, Qiu W, Zhang H, Liang L, Lu D, Zhang K, Gu X, Han L. Chang S, et al. Among authors: zhang k. Front Genet. 2022 Dec 8;13:1062715. doi: 10.3389/fgene.2022.1062715. eCollection 2022. Front Genet. 2022. PMID: 36568374 Free PMC article.

8

Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome.

Du T, Xia Y, Sun C, Gong Z, Liang L, Gong Z, Wang R, Lu D, Zhang K, Yang Y, Sun Y, Sun M, Sun Y, Xiao B, Qiu W. Du T, et al. Among authors: zhang k. Orphanet J Rare Dis. 2024 Feb 16;19(1):75. doi: 10.1186/s13023-024-03070-8. Orphanet J Rare Dis. 2024. PMID: 38365697 Free PMC article.

9

A Novel Mutation in Melanocortin Receptor 2 and a Reported Mutation in Melanocortin Receptor 2 Accessory Protein: Three Chinese Cases with Familial Glucocorticoid Deficiency.

Duan Y, Xia Y, Gong Z, Liu H, Liang L, Zhang K, Yang Y, Wang R, Xiao B, Qiu W. Duan Y, et al. Among authors: zhang k. Mol Syndromol. 2023 Feb;14(1):71-79. doi: 10.1159/000526320. Epub 2022 Oct 11. Mol Syndromol. 2023. PMID: 36777708 Free PMC article.

10

Variable phenotypes and outcomes associated with the MMACHC c.482G > A mutation: follow-up in a large CblC disease cohort.

Wu SN, E HS, Yu Y, Ling SY, Liang LL, Qiu WJ, Zhang HW, Shuai RX, Wei HY, Yang CJ, Xu P, Chen XG, Zou H, Feng JZ, Niu TT, Hu HL, Zhang KC, Lu DY, Gong ZW, Zhan X, Ji WJ, Gu XF, Chen YX, Han LS. Wu SN, et al. World J Pediatr. 2023 Dec 9. doi: 10.1007/s12519-023-00770-2. Online ahead of print. World J Pediatr. 2023. PMID: 38070096

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