نتایج جستجو برای: creatine deficiency syndrome

تعداد نتایج: 748934  

2012
Xueqiang Huang Qunwei Chen Genjin Yang Weixing Dai Qingbo Lang Juan Du Shikai Yan Weidong Zhang Changquan Ling

This study proposes a (1)H NMR-based metabonomic approach to explore the biochemical characteristics of Yang deficiency syndrome in hepatocellular carcinoma (HCC) based on serum metabolic profiling. Serum samples from 21 cases of Yang deficiency syndrome HCC patients (YDS-HCC) and 21 cases of non-Yang deficiency syndrome HCC patients (NYDS-HCC) were analyzed using (1)H NMR spectroscopy and part...

Journal: :Zhong xi yi jie he xue bao = Journal of Chinese integrative medicine 2003
Qin Zhang Ping Liu Hui-Fen Cheng Liang Chen Su-Hua Cao Ying Liu Jian-Jun Wei Zhi-Hong Fang Ding-Zhong Wu

OBJECTIVE To explore the characteristics of traditional Chinese medical syndrome (TCM syndrome) of hepatocirrhosis. METHODS Clinical information from the four diagnosis methods of traditional Chinese medicine (TCM) and related laboratorial indexes were systematically collected from 223 hepatocirrhosis cases, and the multi-statistical methods including systematic cluster analysis, principal co...

Journal: :middle east journal of digestive diseases 0
mohammad javad zahedi sodaif darvish moghadam seyed mahdi seyed mirzaei masood dehghani sara shafiei pour atefe rasti

blue rubber bleb nevus syndrome is a rare disorder that is characterized by multiple recurrent vascular malformations of skin and gastrointestinal tract . the affected patients may present with diverse manifestations including iron deficiency anemia. we report this syndrome in a 22-year-old man that was referred to our hospital for iron deficiency anemia with unknown cause and vascular malforma...

Journal: :Science Translational Medicine 2021

Clinical and basic studies shed light on the mechanism, diagnosis, treatment of cardiac ryanodine receptor Ca 2+ release deficiency syndrome.

2014
Catarina M. Quinzii Valentina Emmanuele Michio Hirano

Coenzyme Q 10 (CoQ 10 ) deficiency is a clinically and genetically heterogeneous syndrome which has been associated with 5 major clinical phenotypes: (1) encephalomyopathy, (2) severe infantile multisystemic disease, (3) nephropathy, (4) cerebellar ataxia, and (5) isolated myopathy. Of these phenotypes, cerebellar ataxia and syndromic or isolated nephrotic syndrome are the most common. CoQ 10 d...

2011
Hirohide Yokokawa Ikiko Kinoshita Takeo Hashiguchi Masako Kako Kahoru Sasaki Akira Tamura Yuri Kintaka Yoko Suzuki Noriko Ishizuka Katsumi Arai Yoshiko Kasahara Mikiko Kishi Yoko Kobayashi Tosei Takahashi Hiroyuki Shimizu Shuji Inoue

UNLABELLED Aims/Introduction:  The effects of 5-day voluntary exercise on muscle damage and muscle protein degradation were investigated in a streptozotocin-induced rat model of moderately glycemic, uncontrolled, type 2 diabetes. MATERIALS AND METHODS   In the preliminary experiment, an oral glucose tolerance (1.0 g/kg) test was carried out to confirm the development of diabetes 3 days after ...

2013
Yubo Li Yuxiu Sun Xueling Ma Xiaoxing Xue Xinlou Chai Weiming Wang Huihui Zhao Kun Chen Shuzhen Guo Jianxin Chen Wei Wang Huan Dong Lu

The objective of the present study was to make comparison between rat models of depression achieved by chronic unpredictable mild stress (CUMS) and reserpine injection from the angle of traditional Chinese medicine syndrome, depict the regularity of syndrome variation of the two models, and preliminarily explain its molecular mechanism. Rat depression models were achieved respectively by CUMS a...

Journal: :Kidney & blood pressure research 2014
Ahmad Almilaji Mentor Sopjani Bernat Elvira José Borras Miribane Dërmaku-Sopjani Carlos Munoz Jamshed Warsi Undine E Lang Florian Lang

BACKGROUND/AIMS The transmembrane Klotho protein contributes to inhibition of 1,25(OH)2D3 formation. The extracellular domain of Klotho protein could function as an enzyme with e.g. β-glucuronidase activity, be cleaved off and be released into blood and cerebrospinal fluid. Klotho regulates several cellular transporters. Klotho protein deficiency accelerates the appearance of age related disord...

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