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Author:( Zhiyan LU)

1.Experimental Study of Sanshanxiao Granules on the Levels of Insulin and Lipid Peroxidation in Model Rats of Diabetes

Zhiyan LU ; Yuyun HUANG ; Nianping ZHANG

Chinese Journal of Information on Traditional Chinese Medicine 2006;0(10):-

2.Mitochondrial DNA deletion on the growth and invasiveness of human lung cancer cells

Xianlong LING ; Yinglin LU ; Zhiyan DU

Journal of Third Military Medical University 2003;0(14):-

3.Imaging Diagnosis and Interventional Therapy of Diffuse Type Hepatic Cellular Carcinoma (A Report of 14 Cases )

Junfang LIU ; Qingyun LONG ; Jinxiang HU ; Zhiyan LU ; Deqiang ZHUO

Journal of Practical Radiology 2001;0(01):-

4.The diagnosis applying effects of ocular vestibular evoked myogenic potentials in BBPV disease.

Baocai LU ; Wenfu YU ; Zhiyan WU ; Rong LIAN ; Zhenmin LU ; Jianbin YANG

Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2015;29(14):1256-1259

5.Analysis of related factors of contrast-enhanced ultrasonography in evaluating renal traumatic degree

Zhiyan LI ; Jie TANG ; Yukun LUO ; Faqin LU ; Tengfei Yü ; Jiangke TIAN ; Xia XIE

Chinese Journal of Ultrasonography 2012;21(4):348-351

6.Mutuality analysis on quickly evaluate the traumatic degree of abdominal solid-organs with contrast-enhanced ultrasonography

Zhiyan LI ; Jie TANG ; Yukun LUO ; Faqin LU ; Yu TANG ; Jiangke TIAN

Chinese Journal of Ultrasonography 2012;21(9):779-783

7.Comparative analysis of cognitive function and neuropsychiatric behavior between Alzheimer's disease and frontotemporal dementia patients

Pan LI ; Yuying ZHOU ; Zhiyan TIAN ; Da LU ; Huihong ZHANG ; Shuai LIU

Chinese Journal of Neurology 2014;47(9):610-616

8.Imaging evaluation of complications after liver transplantation

Mingyue WANG ; Zhiyan LU

Journal of Clinical Hepatology 2016;32(12):2295-

9.Clinical phenotype and analysis of CHD7 gene variants in three children patients with CHARGE syndrome.

Zhiyan TAO ; Fang LU

Chinese Journal of Medical Genetics 2021;38(1):42-46

10.Genetic and phenotypic analysis of a patient with phosphogylcerate dehydrogenase deficiency.

Zhiyan TAO ; Fang LU

Chinese Journal of Medical Genetics 2021;38(2):170-173

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