Wu BB - Search Results

1

Cholestasis as a dominating symptom of patients with CYP27A1 mutations: An analysis of 17 Chinese infants.

Zhang P, Zhao J, Peng XM, Qian YY, Zhao XM, Zhou WH, Wang JS, Wu BB, Wang HJ. Zhang P, et al. Among authors: wu bb. J Clin Lipidol. 2021 Jan-Feb;15(1):116-123. doi: 10.1016/j.jacl.2020.12.004. Epub 2020 Dec 14. J Clin Lipidol. 2021. PMID: 33414089

2

Clinical and genetic features of Prader-Willi syndrome in China.

Lu W, Qi Y, Cui B, Chen XL, Wu BB, Chen C, Cao Y, Zhou WH, Xu H, Luo FH. Lu W, et al. Among authors: wu bb. Eur J Pediatr. 2014 Jan;173(1):81-6. doi: 10.1007/s00431-013-2124-2. Epub 2013 Aug 11. Eur J Pediatr. 2014. PMID: 23933672

3

The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency.

Wang NL, Li LT, Wu BB, Gong JY, Abuduxikuer K, Li G, Wang JS. Wang NL, et al. Among authors: wu bb. PLoS One. 2016 Apr 6;11(4):e0153114. doi: 10.1371/journal.pone.0153114. eCollection 2016. PLoS One. 2016. PMID: 27050426 Free PMC article.

4

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions.

Wang NL, Lu YL, Zhang P, Zhang MH, Gong JY, Lu Y, Xie XB, Qiu YL, Yan YY, Wu BB, Wang JS. Wang NL, et al. Among authors: wu bb. PLoS One. 2016 Oct 5;11(10):e0164058. doi: 10.1371/journal.pone.0164058. eCollection 2016. PLoS One. 2016. PMID: 27706244 Free PMC article.

5

Relationship between phenotype and genotype of 102 Chinese newborns with Prader-Willi syndrome.

Ge MM, Gao YY, Wu BB, Yan K, Qin Q, Wang H, Zhou W, Yang L. Ge MM, et al. Among authors: wu bb. Mol Biol Rep. 2019 Oct;46(5):4717-4724. doi: 10.1007/s11033-019-04916-2. Epub 2019 Jul 3. Mol Biol Rep. 2019. PMID: 31270759

6

Identification of eight novel mutations in 11 Chinese patients with maple syrup urine disease.

Sun WH, Wu BB, Wang YQ, Wu MY, Dong XR, Zhang YP, Lu W, Zhang P, Yang B, Zhang M, Wu HJ, Zhou WH. Sun WH, et al. Among authors: wu bb, wu hj, wu my. World J Pediatr. 2020 Aug;16(4):401-410. doi: 10.1007/s12519-020-00349-1. Epub 2020 Mar 19. World J Pediatr. 2020. PMID: 32193832

7

[Clinical features and SLC6A8 gene mutations of cerebral creatine deficiency syndrome I: an analysis of two families].

Sun WH, Zhuang DY, Wang Y, Xiao FF, Wu MY, Dong XR, Zhang P, Wang HJ, Zhou WH, Wu BB. Sun WH, et al. Among authors: wu bb, wu my. Zhongguo Dang Dai Er Ke Za Zhi. 2020 May;22(5):482-487. doi: 10.7499/j.issn.1008-8830.2002012. Zhongguo Dang Dai Er Ke Za Zhi. 2020. PMID: 32434645 Free PMC article. Chinese.

8

A term neonate with early myoclonic encephalopathy caused by RARS2 gene variants: a case report.

Xu Y, Wu BB, Wang HJ, Zhou SZ, Cheng GQ, Zhou YF. Xu Y, et al. Among authors: wu bb. Transl Pediatr. 2020 Oct;9(5):707-712. doi: 10.21037/tp-20-110. Transl Pediatr. 2020. PMID: 33209735 Free PMC article.

9

Genetic etiologies associated with infantile hydrocephalus in a Chinese infantile cohort.

Mei HF, Dong XR, Chen HY, Lu YL, Wu BB, Wang HJ, Cheng GQ, Wang LS, Cao Y, Yang L, Zhou WH. Mei HF, et al. Among authors: wu bb. World J Pediatr. 2021 Jun;17(3):305-316. doi: 10.1007/s12519-021-00429-w. Epub 2021 Apr 29. World J Pediatr. 2021. PMID: 33914258

10

Potential protein-phenotype correlation in three lipopolysaccharide-responsive beige-like anchor protein-deficient patients.

Tang WJ, Hu WH, Huang Y, Wu BB, Peng XM, Zhai XW, Qian XW, Ye ZQ, Xia HJ, Wu J, Shi JR. Tang WJ, et al. Among authors: wu bb, wu j. World J Clin Cases. 2021 Jul 26;9(21):5873-5888. doi: 10.12998/wjcc.v9.i21.5873. World J Clin Cases. 2021. PMID: 34368306 Free PMC article.

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