HuGE Literature Finder
Records
1
-
22
[Hereditary Spherocytosis and Pregnancy: A Case Report]. Acta medica portuguesa 2023 2 . Miguel Andreia, Alves Maria José, Massa Ana Catari |
MTHFR polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: An observational study. Frontiers in neurology 2023 1 13 1074857. Guo Jianhao, Hao Xing, Wang Rongrong, Lian Ke, Jiang Jun, Chen Na, Feng Zhiying, Rao Yuefe |
Identification of SNPs associated with methotrexate treatment outcomes in patients with early rheumatoid arthritis. Frontiers in pharmacology 2022 12 13 1075603. Kolan Shrikant S, Li Gaoyang, Grimolizzi Franco, Sexton Joe, Goll Guro, Kvien Tore K, Sundlisæter Nina Paulshus, Zucknick Manuela, Lillegraven Siri, Haavardsholm Espen A, Skålhegg Bjørn Ste |
T677T Methylenetetrahydrofolate Reductase Single Nucleotide Polymorphisms Increased Prevalence in a Subgroup of Infertile Patients with Endometriosis. Journal of women's health (2002) 2022 7 31 (10): 1501-1506. Clément Patrice, Alvarez Silvia, Jacquesson-Fournols Laetitia, Cornet Dominique, Clément Arthur, Brack Michel, Lalau-Keraly Marc, Delafontaine Didier, Cohen Marc, Menezo Yv |
Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
Investigation of ACE rs4646994, MTHFR rs1801133 and VDR rs2228570 Genotypes in Jordanian Patients with Fibromyalgia Syndrome. Endocrine, metabolic & immune disorders drug targets 2020 Dec . Khalil Raida, Al-Awaida Wajdy J, Al-Ameer Hamzeh J, Jarrar Yazun, Imraish Amer, Al Bawareed Omar, Qawadri Rand, Al Madhoon Farah, Obeidat Lo |
Clinical and Laboratory Associations with Methotrexate Metabolism Gene Polymorphisms in Rheumatoid Arthritis. Journal of personalized medicine 2020 9 10 (4): . D'Cruz Leon G, McEleney Kevin G, Tan Kyle B C, Shukla Priyank, Gardiner Philip V, Connolly Patricia, Conway Caroline, Cobice Diego, Gibson David |
Investigation of MTHFR gene C677T polymorphism in cardiac syndrome X patients. Journal of clinical laboratory analysis 2017 May . Kandaz Cemre, Önal Burak, Özen Deniz, Demir Bülent, Akkan A Gökhan, Özyazgan Sib |
MTHFR and ACE Polymorphisms Do Not Increase Susceptibility to Migraine Neither Alone Nor in Combination. Headache 2016 Aug . Essmeister Rafaela, Kress Hans-Georg, Zierz Stephan, Griffith Lyn, Lea Rod, Wieser Thom |
Molecular factors in migraine. Oncotarget 2016 May . Kowalska Marta, Prendecki MichaÅ, Kozubski Wojciech, Lianeri Margarita, Dorszewska Jolan |
Preliminary study for predicting better methotrexate efficacy in Japanese patients with rheumatoid arthritis. Journal of pharmaceutical health care and sciences 2016 2 13. Hashiguchi Masayuki, Tsuru Tomomi, Miyawaki Kumika, Suzaki Midori, Hakamata Jun, Shimizu Mikiko, Irie Shin, Mochizuki Mayu |
Angiotensin converting enzyme and methylenetetrahydrofolate reductase gene variations in fibromyalgia syndrome. Gene 2015 Jun 564 (2): 188-92. Inanir Ahmet, Yigit Serbulent, Tekcan Akin, Pinarli Ferda Alpaslan, Inanir Sema, Karakus Nev |
Epistasis between polymorphisms in COMT, ESR1, and GCH1 influences COMT enzyme activity and pain. Pain 2014 Nov 155 (11): 2390-9. Smith Shad B, Reenilä Ilkka, Männistö Pekka T, Slade Gary D, Maixner William, Diatchenko Luda, Nackley Andrea |
Clinical impact of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations among sickle cell disease patients of Central India. European journal of haematology 2013 Sep . Nishank SS, Singh M, Yadav R |
Homocysteine plasma levels in patients treated with antiepileptic drugs depend on folate and vitamin B12 serum levels, but not on genetic variants of homocysteine metabolism. Clinical chemistry and laboratory medicine : CCLM / FESCC 2013 Feb . Semmler A, Moskau-Hartmann S, Stoffel-Wagner B, Elger C, Linnebank M |
Fibromyalgia, mood disorders, and intense creative energy: A1AT polymorphisms are not always silent. Neurotoxicology 2012 Dec 33 (6): 1454-72. Schmechel Donald E, Edwards Christopher |
Genotypes of the MTHFR C677T and MTRR A66G genes act independently to reduce migraine disability in response to vitamin supplementation. Pharmacogenetics and genomics 2012 Oct 22 (10): 741-9. Menon Saras, Lea Rod A, Roy Bishakha, Hanna Michelle, Wee Shirley, Haupt Larisa M, Oliver Chris, Griffiths Lyn |
Analysis of the MTHFR C677T variant with migraine phenotypes. BMC research notes 2010 3 (1): 213. Liu Annie, Menon Saraswathy, Colson Natalie J, Quinlan Sharon, Cox Hannah, Peterson Madelyn, Tiang Thomas, Haupt Larisa M, Lea Rod A, Griffiths Lyn |
Endothelial cell dysfunction in women with cardiac syndrome X and MTHFR C677T mutation. The Israel Medical Association journal : IMAJ 2007 Apr 9 (4): 321-5. Alroy Sharon, Preis Meir, Barzilai Menashe, Cassel Aliza, Lavie Lena, Halon David A, Amir Ofer, Lewis Basil S, Flugelman Moshe |
Stromelysin-1 5A/6A and eNOS T-786C polymorphisms, MTHFR C677T and A1298C mutations, and cigarette-cannabis smoking: a pilot, hypothesis-generating study of gene-environment pathophysiological associations with Buerger's disease. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2006 Oct 12 (4): 427-39. Glueck Charles J, Haque Mofiz, Winarska Magdalena, Dharashivkar Swapna, Fontaine Robert N, Zhu Binghua, Wang Pi |
Frequency of thrombophilia-related genetic variations in patients with idiopathic pulmonary embolism in an urban emergency department. Clinical chemistry 2006 Jun 52 (6): 1026-32. Kruse Lori, Mitchell Alice M, Camargo Carlos A, Hernandez Jackeline, Kline Jeffrey |
The methylenetetrahydrofolate reductase gene polymorphism (C677T) is associated with increased cardiovascular mortality in Hungary. International journal of cardiology 2004 Nov 97 (2): 333-4. Kalina Akos, Czeizel Andrew |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 22, 2023
- Content source: