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Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients.
Fan Y, Tan D, Song D, Zhang X, Chang X, Wang Z, Zhang C, Chan SH, Wu Q, Wu L, Wang S, Yan H, Ge L, Yang H, Mao B, Bönnemann C, Liu J, Wang S, Yuan Y, Wu X, Zhang H, Xiong H. Fan Y, et al. Among authors: yan h. J Med Genet. 2021 May;58(5):326-333. doi: 10.1136/jmedgenet-2019-106671. Epub 2020 Jun 22. J Med Genet. 2021. PMID: 32571898 Free PMC article.
Comorbidity of chronic fatigue syndrome, postural tachycardia syndrome, and narcolepsy with 5,10-methylenetetrahydrofolate reductase (MTHFR) mutation in an adolescent: a case report.
Liao Y, Qi JG, Yan H, Zhang QY, Ji TY, Chang XZ, Yang HP, Jin HF, Du JB. Liao Y, et al. Among authors: yan h. Chin Med J (Engl). 2021 Mar 25;134(12):1495-1497. doi: 10.1097/CM9.0000000000001387. Chin Med J (Engl). 2021. PMID: 33788782 Free PMC article. No abstract available.
A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemia.
Kang L, Liu Y, Shen M, Liu Y, He R, Song J, Jin Y, Li M, Zhang Y, Dong H, Liu X, Yan H, Qin J, Zheng H, Chen Y, Li D, Wei H, Zhang H, Sun L, Zhu Z, Liang D, Yang Y. Kang L, et al. Among authors: yan h. J Inherit Metab Dis. 2020 May;43(3):409-423. doi: 10.1002/jimd.12183. Epub 2019 Nov 26. J Inherit Metab Dis. 2020. PMID: 31622506
Spontaneous Rupture and Thrombosis of Right Atrium.
Li FF, Zhou YJ, Yan H. Li FF, et al. Among authors: yan h. Chin Med J (Engl). 2018 Jan 20;131(2):241-242. doi: 10.4103/0366-6999.222329. Chin Med J (Engl). 2018. PMID: 29336375 Free PMC article. No abstract available.
14,591 results
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