Zobrazeno 1 - 10
of 321
pro vyhledávání: '"Yuan Hj"'
Association of Serum Uric Acid with Non-Valvular Atrial Fibrillation: A Retrospective Study in China
Publikováno v:
International Journal of General Medicine, Vol Volume 17, Pp 1533-1543 (2024)
Hua-Jing Yuan,1 Hua-Chen Jiao,2 Xiu-Juan Liu,2 Hao Hao,2 Yang Liu,2 Yi-Tao Xue,2 Yan Li2 1Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, 250014, People’s Republic of China; 2Affiliated Hospital of Shandong University
Externí odkaz:
https://doaj.org/article/4038f60b6ae14b8facdfff53d4ec0f2a
Publikováno v:
Balkan Journal of Medical Genetics, Vol 21, Iss 1, Pp 53-57 (2018)
Mitochondrial DNA (mtDNA) mutations have long been proposed to play important roles in the pathogenesis of diabetes mellitus (DM). A large proportion of these mutations are localized at the mt-tRNA genes. Owing to its high mutation rate, a growing nu
Externí odkaz:
https://doaj.org/article/47e466feab6a4933872836a81b6baabe
Autor:
Liang-Jun Xie, Mu-Hua Cheng, Zhou Hj, Feng Zhang, Yi Chen, Feng-wei Zeng, Luping Qin, Jian-fang Li, Yuan Hj
Publikováno v:
European Journal of Clinical Nutrition. 69:856-861
The objective of this study was to investigate body composition redistribution at 3 months after radioactive iodine therapy (RAI).Eighty patients with Graves' disease (GD) for RAI and 18 volunteers were recruited. All patients underwent thyroid statu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fb33a60e434e1c4623aca602c96031c
https://doi.org/10.1038/ejcn.2014.232
https://doi.org/10.1038/ejcn.2014.232
Autor:
Feng L, Pu Dai, Qin W, Yuan Hj, Weiyan Yang, Sun Q, Cao Jy, Lin He, Jing Cheng, Sun Hj, Yan D, Dongyi Han, Yuqian Wang, Xuezhong Liu, Xiaomei Ouyang, Suoqiang Zhai, Shiming Yang, Tao R, Feng Gy, Simon I. Angeli
Publikováno v:
Clinical Genetics. 73:391-394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bad4275915c2fa0a9cdf852dc6eaadb7
https://doi.org/10.1111/j.1399-0004.2008.00972.x
https://doi.org/10.1111/j.1399-0004.2008.00972.x
Autor:
Weiyan Yang, Qin W, Jing Cheng, Xiaomei Ouyang, Sun Q, Feng Gy, Cao Jy, Suoqiang Zhai, Sun Hj, Lin He, Pu Dai, Zhang Yz, Dongyi Han, Yuan Hj, Xuezhong Liu, Yan D, Wang Hy, L. L. Du, Shiming Yang, Tao R
Publikováno v:
Clinical Genetics. 72:471-477
We report here the clinical, genetic, and molecular characteristics of a large Chinese family exhibiting non-syndromic, late-onset autosomal dominant sensorineural hearing loss. Clinical evaluation revealed variable phenotypes of hearing loss in term
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76324b32e1c5166a967f200ab261da32
https://doi.org/10.1111/j.1399-0004.2007.00889.x
https://doi.org/10.1111/j.1399-0004.2007.00889.x
Publikováno v:
Balkan Journal of Medical Genetics; Jun2018, Vol. 21 Issue 1, p53-57, 5p
Publikováno v:
Physiological research. 60(2)
We previously demonstrated in rats that noninvasive delayed limb ischemic preconditioning (LIPC) induced by three cycles of 5-min occlusion and 5-min reperfusion of the left hind limb per day for three days confers the same cardioprotective effect as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7d6f596ebf2db2b41d54b9771426e40
https://pubmed.ncbi.nlm.nih.gov/21114361
https://pubmed.ncbi.nlm.nih.gov/21114361
Autor:
Hong, Tao R, Yu Lm, Cao Jy, Yuan Hj, Jing Cheng, Sun Hj, Han Dy, Feng Gy, Lin He, Yang Sz, Pu Dai
Publikováno v:
Yi chuan = Hereditas. 28(12)
Hereditary non-syndromic sensorineural hearing loss is a genetically highly heterogeneous group of disorders. To date, at least 50 loci for autosomal dominant non-syndromic sensorineural hearing loss (DFNA) have been identified by linkage analysis. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe639a7875485af0ff7013cf532d54d3
https://pubmed.ncbi.nlm.nih.gov/17138532
https://pubmed.ncbi.nlm.nih.gov/17138532
Publikováno v:
Balkan Journal of Medical Genetics; October 2018, Vol. 21 Issue: 1 p53-57, 5p
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