Zhu Y - Search Results

1

Muscle Magnetic Resonance Imaging in Patients with Various Clinical Subtypes of LMNA-Related Muscular Dystrophy.

Lin HT, Liu X, Zhang W, Liu J, Zuo YH, Xiao JX, Zhu Y, Yuan Y, Wang ZX. Lin HT, et al. Among authors: zhu y. Chin Med J (Engl). 2018 Jun 20;131(12):1472-1479. doi: 10.4103/0366-6999.233957. Chin Med J (Engl). 2018. PMID: 29893365 Free PMC article.

2

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina.

Zhang W, Zhou X, Liu L, Zhu Y, Liu C, Pan H, Xing Q, Wang J, Wang X, Zhang X, Cao Y, Wang B. Zhang W, et al. Among authors: zhu y. Oncotarget. 2017 Jan 31;8(5):8785-8790. doi: 10.18632/oncotarget.14455. Oncotarget. 2017. PMID: 28061432 Free PMC article.

3

3.0 T magnetic resonance myocardial perfusion imaging for semi-quantitative evaluation of coronary microvascular dysfunction in hypertrophic cardiomyopathy.

Yin L, Xu HY, Zheng SS, Zhu Y, Xiao JX, Zhou W, Yu SS, Gong LG. Yin L, et al. Among authors: zhu y. Int J Cardiovasc Imaging. 2017 Dec;33(12):1949-1959. doi: 10.1007/s10554-017-1189-9. Epub 2017 Jun 13. Int J Cardiovasc Imaging. 2017. PMID: 28612277

4

Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing.

Wang B, Li L, Zhu Y, Zhang W, Wang X, Chen B, Li T, Pan H, Wang J, Kee K, Cao Y. Wang B, et al. Among authors: zhu y. Hum Reprod. 2017 Oct 1;32(10):2138-2146. doi: 10.1093/humrep/dex263. Hum Reprod. 2017. PMID: 28938739

5

A novel homozygous mutation of bone morphogenetic protein 15 identified in a consanguineous marriage family with primary ovarian insufficiency.

Zhang W, Wang J, Wang X, Li L, Pan H, Chen B, Zhu Y, Li T, Cao Y, Wang B. Zhang W, et al. Among authors: zhu y. Reprod Biomed Online. 2018 Feb;36(2):206-209. doi: 10.1016/j.rbmo.2017.10.104. Epub 2017 Oct 26. Reprod Biomed Online. 2018. PMID: 29169851

6

3D pseudocontinuous arterial spin-labeling perfusion imaging detected crossed cerebellar diaschisis in acute, subacute and chronic intracerebral hemorrhage.

Yin L, Cheng S, Xiao J, Zhu Y, Bu S, Zhang X, Liu R, Huang Y, Xie S. Yin L, et al. Among authors: zhu y. Clin Imaging. 2018 Jul-Aug;50:37-42. doi: 10.1016/j.clinimag.2017.12.007. Epub 2017 Dec 15. Clin Imaging. 2018. PMID: 29258030

7

FHL1-related clinical, muscle MRI and genetic features in six Chinese patients with reducing body myopathy.

Hu Z, Zhu Y, Liu X, Zhang W, Liu J, Wu S, Xiao J, Yuan Y, Wang Z. Hu Z, et al. Among authors: zhu y. J Hum Genet. 2019 Sep;64(9):919-926. doi: 10.1038/s10038-019-0627-z. Epub 2019 Jul 4. J Hum Genet. 2019. PMID: 31273321 Clinical Trial.

8

Novel TTN mutations and muscle imaging characteristics in congenital titinopathy.

Yu M, Zhu Y, Xie Z, Zheng Y, Xiao J, Zhang W, Nishino I, Yuan Y, Wang Z. Yu M, et al. Among authors: zhu y. Ann Clin Transl Neurol. 2019 Jul;6(7):1311-1318. doi: 10.1002/acn3.50831. Epub 2019 Jul 1. Ann Clin Transl Neurol. 2019. PMID: 31353864 Free PMC article.

9

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: zhu y. 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.

10

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: zhu y. 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.

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