Wang Z - Search Results

1

Rare diseases in China: analysis of 2014-2015 hospitalization summary reports for 281 rare diseases from 96 tertiary hospitals.

Shi X, Liu H, Zhan S, Wang Z, Wang L, Dong C, Wang Y, Yao C, Ding J, Li Y. Shi X, et al. Among authors: wang l, wang z, wang y. Orphanet J Rare Dis. 2019 Jul 1;14(1):160. doi: 10.1186/s13023-019-1137-y. Orphanet J Rare Dis. 2019. PMID: 31262329 Free PMC article.

2

Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients.

Xie Z, Hou Y, Yu M, Liu Y, Fan Y, Zhang W, Wang Z, Xiong H, Yuan Y. Xie Z, et al. Among authors: wang z. Orphanet J Rare Dis. 2019 Feb 14;14(1):43. doi: 10.1186/s13023-019-1021-9. Orphanet J Rare Dis. 2019. PMID: 30764848 Free PMC article.

3

Characteristics of Pompe disease in China: a report from the Pompe registry.

Zhao Y, Wang Z, Lu J, Gu X, Huang Y, Qiu Z, Wei Y, Yan C. Zhao Y, et al. Among authors: wang z. Orphanet J Rare Dis. 2019 Apr 3;14(1):78. doi: 10.1186/s13023-019-1054-0. Orphanet J Rare Dis. 2019. PMID: 30943998 Free PMC article.

4

Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex.

Xie Z, Xie Z, Yu M, Zheng Y, Sun C, Liu Y, Ling C, Zhu Y, Zhang W, Xiao J, Wang Z, Yuan Y. Xie Z, et al. Among authors: wang z. Orphanet J Rare Dis. 2019 Nov 12;14(1):250. doi: 10.1186/s13023-019-1242-y. Orphanet J Rare Dis. 2019. PMID: 31747956 Free PMC article.

5

Demographic characteristics, diagnostic challenges, treatment patterns, and caregiver burden of mitochondrial diseases: a retrospective cross-sectional study.

Zhao X, Yu M, Zhang W, Hou Y, Yuan Y, Wang Z. Zhao X, et al. Among authors: wang z. Orphanet J Rare Dis. 2024 Aug 2;19(1):287. doi: 10.1186/s13023-024-03289-5. Orphanet J Rare Dis. 2024. PMID: 39095827 Free PMC article.

6

Neutral lipid storage disease with myopathy in China: a large multicentric cohort study.

Zhang W, Wen B, Lu J, Zhao Y, Hong D, Zhao Z, Zhang C, Luo Y, Qi X, Zhang Y, Song X, Zhao Y, Zhao C, Hu J, Yang H, Wang Z, Yan C, Yuan Y. Zhang W, et al. Among authors: wang z. Orphanet J Rare Dis. 2019 Oct 26;14(1):234. doi: 10.1186/s13023-019-1209-z. Orphanet J Rare Dis. 2019. PMID: 31655616 Free PMC article.

7

Factors associated with refractory autoimmune necrotizing myopathy with anti-signal recognition particle antibodies.

Zhao Y, Zhang W, Liu Y, Wang Z, Yuan Y. Zhao Y, et al. Among authors: wang z. Orphanet J Rare Dis. 2020 Jul 8;15(1):181. doi: 10.1186/s13023-020-01431-7. Orphanet J Rare Dis. 2020. PMID: 32641139 Free PMC article.

8

Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations.

Yu M, Zhu Y, Lu Y, Lv H, Zhang W, Yuan Y, Wang Z. Yu M, et al. Among authors: wang z. Orphanet J Rare Dis. 2020 Dec 9;15(1):344. doi: 10.1186/s13023-020-01626-y. Orphanet J Rare Dis. 2020. PMID: 33298082 Free PMC article.

9

Ultrasound-guided interlaminar approach for nusinersen administration in patients with spinal muscular atrophy with spinal fusion or severe scoliosis.

Wei C, Liang Z, Wu Y, Liu S, Qiu J, Meng L, Li C, Li S, Bao X, Wang Z, Chen L, Xiong H. Wei C, et al. Among authors: wang z. Orphanet J Rare Dis. 2023 Feb 17;18(1):30. doi: 10.1186/s13023-023-02630-8. Orphanet J Rare Dis. 2023. PMID: 36800969 Free PMC article.

10

Clinical and genetic interpretation of uncertain DMD missense variants: evidence from mRNA and protein studies.

Xie Z, Liu C, Yu H, Xie Z, Sun C, Zhu Y, Hu X, Bai L, Wei L, Sun P, Lu Y, Lu Y, Zhao Y, Zhang W, Wang Z, Meng L, Yuan Y. Xie Z, et al. Among authors: wang z. Orphanet J Rare Dis. 2024 Mar 14;19(1):123. doi: 10.1186/s13023-024-03128-7. Orphanet J Rare Dis. 2024. PMID: 38486238 Free PMC article.

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