Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Syndrome and COX2[original query] |
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| A case of Kearns-Sayre syndrome with the 4,977-bp common deletion associated with a novel 7,704-bp deletion. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2003 1 23 (5): 247-50. Vázquez-Acevedo M, Vázquez-Memije M E, Mutchinick O M, Morales J J, García-Ramos G, González-Halphen |
| Associations between COX-2 polymorphisms, blood cholesterol and risk of acute coronary syndrome. Atherosclerosis 2010 Mar 209 (1): 155-62. Vogel Ulla, Segel Stine, Dethlefsen Claus, Tjønneland Anne, Saber Anne Thoustrup, Wallin Håkan, Jensen Majken K, Schmidt Erik B, Andersen Paal Skytt, Overvad K |
| Clinical and molecular characterization of pediatric mitochondrial disorders in south of China. European journal of medical genetics 2020 4 63 (8): 103898. Hu Chaoping, Li Xihua, Zhao Lei, Shi Yiyun, Zhou Shuizhen, Wu Bingbing, Wang |
| Elevated Levels of PGE2-Metabolite in Cerebrospinal Fluid and Cox-2 Gene Polymorphisms in Patients with Chronic, Post Cholecystectomy Pain and Visceral Hyperalgesia Compared to Healthy Controls. A Hypothesis-Generating Pilot Study. Journal of pain research 2022 12 15 3921-3929. Blichfeldt-Eckhardt Morten Rune, Olsen Dorte Aalund, Andersen Rikke Fredslund, Toft Palle, Bendix Lai |
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