127 related articles for article (PubMed ID: 11597779)
1. Significance of the catechol-O-methyltransferase gene polymorphism in migraine.
Emin Erdal M; Herken H; Yilmaz M; Bayazit YA
Brain Res Mol Brain Res; 2001 Oct; 94(1-2):193-6. PubMed ID: 11597779
[TBL] [Abstract][Full Text] [Related]
2. The functional Val158Met variant of the COMT gene is not associated with migraine with or without aura.
Mössner R; Freitag CM; Marziniak M; Moser D; Sommer C; Meyer J
J Headache Pain; 2006 Jun; 7(3):165-6. PubMed ID: 16767536
[No Abstract] [Full Text] [Related]
3. Association of the T102C polymorphism of 5-HT2A receptor gene with aura in migraine.
Erdal ME; Herken H; Yilmaz M; Bayazit YA
J Neurol Sci; 2001 Jul; 188(1-2):99-101. PubMed ID: 11489292
[TBL] [Abstract][Full Text] [Related]
4. Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome.
Gürsoy S; Erdal E; Herken H; Madenci E; Alaşehirli B; Erdal N
Rheumatol Int; 2003 May; 23(3):104-7. PubMed ID: 12739038
[TBL] [Abstract][Full Text] [Related]
5. Genetic contribution of catechol-O-methyltransferase in hippocampal structural and functional changes of female migraine sufferers.
Liu J; Lan L; Mu J; Zhao L; Yuan K; Zhang Y; Huang L; Liang F; Tian J
Hum Brain Mapp; 2015 May; 36(5):1782-95. PubMed ID: 25598522
[TBL] [Abstract][Full Text] [Related]
6. The C677T polymorphism in MTHFR is not associated with migraine in Portugal.
Ferro A; Castro MJ; Lemos C; Santos M; Sousa A; Pereira-Monteiro J; Sequeiros J; Maciel P
Dis Markers; 2008; 25(2):107-13. PubMed ID: 18957721
[TBL] [Abstract][Full Text] [Related]
7. MTHFR T677 homozygosis influences the presence of aura in migraineurs.
Oterino A; Valle N; Bravo Y; Muñoz P; Sánchez-Velasco P; Ruiz-Alegría C; Castillo J; Leyva-Cobián F; Vadillo A; Pascual J
Cephalalgia; 2004 Jun; 24(6):491-4. PubMed ID: 15154859
[TBL] [Abstract][Full Text] [Related]
8. Look beyond Catechol-O-Methyltransferase genotype for cathecolamines derangement in migraine: the BioBIM rs4818 and rs4680 polymorphisms study.
De Marchis ML; Barbanti P; Palmirotta R; Egeo G; Aurilia C; Fofi L; Piroso S; Ialongo C; Della-Morte D; D'Andrea G; Ferroni P; Guadagni F
J Headache Pain; 2015; 16():520. PubMed ID: 25929431
[TBL] [Abstract][Full Text] [Related]
9. Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.
Lachman HM; Papolos DF; Saito T; Yu YM; Szumlanski CL; Weinshilboum RM
Pharmacogenetics; 1996 Jun; 6(3):243-50. PubMed ID: 8807664
[TBL] [Abstract][Full Text] [Related]
10. No associations between five polymorphisms in COMT gene and migraine.
Takigawa H; Kowa H; Nakashima K
Acta Neurol Scand; 2017 Feb; 135(2):225-230. PubMed ID: 26988620
[TBL] [Abstract][Full Text] [Related]
11. Lack of association of catechol-O-methyltransferase gene polymorphism in obsessive-compulsive disorder.
Erdal ME; Tot S; Yazici K; Yazici A; Herken H; Erdem P; Derici E; Camdeviren H
Depress Anxiety; 2003; 18(1):41-5. PubMed ID: 12900951
[TBL] [Abstract][Full Text] [Related]
12. Genetic Contribution of Catechol-O-methyltransferase Polymorphism in Patients with Migraine without Aura.
Park JW; Lee KS; Kim JS; Kim YI; Shin HE
J Clin Neurol; 2007 Mar; 3(1):24-30. PubMed ID: 19513339
[TBL] [Abstract][Full Text] [Related]
13. An opposite-direction modulation of the COMT Val158Met polymorphism on the clinical response to intrathecal morphine and triptans.
Cargnin S; Magnani F; Viana M; Tassorelli C; Mittino D; Cantello R; Sances G; Nappi G; Canonico PL; Genazzani AA; Raffaeli W; Terrazzino S
J Pain; 2013 Oct; 14(10):1097-106. PubMed ID: 23773341
[TBL] [Abstract][Full Text] [Related]
14. Genetic susceptibility of catechol-O-methyltransferase polymorphism in Japanese patients with breast cancer.
Inoue H; Shibuta K; Matsuyama A; Yoshinaga K; Sadanaga N; Ueo H; Barnard GF; Mori M
Oncol Rep; 2005 Sep; 14(3):707-12. PubMed ID: 16077979
[TBL] [Abstract][Full Text] [Related]
15. Catechol-O-methyltransferase polymorphism and endometriosis.
Wieser F; Wenzl R; Tempfer C; Worda C; Huber J; Schneeberger C
J Assist Reprod Genet; 2002 Jul; 19(7):343-8. PubMed ID: 12168735
[TBL] [Abstract][Full Text] [Related]
16. Relationship between the Val158Met polymorphism of catechol O-methyl transferase and breast cancer.
Yim DS; Parkb SK; Yoo KY; Yoon KS; Chung HH; Kang HL; Ahn SH; Noh DY; Choe KJ; Jang IJ; Shin SG; Strickland PT; Hirvonen A; Kang D
Pharmacogenetics; 2001 Jun; 11(4):279-86. PubMed ID: 11434504
[TBL] [Abstract][Full Text] [Related]
17. [Polymorphism of catechol-O-methyltransferase gene in relation to the risk of endometrial cancer].
Zhao XM; Xie MQ; Yang DZ; Wang LA; Li SJ; Zhuang YY; Tang XL
Zhonghua Fu Chan Ke Za Zhi; 2007 Feb; 42(2):116-9. PubMed ID: 17442187
[TBL] [Abstract][Full Text] [Related]
18. Functional catechol-O-methyltransferase gene polymorphism and susceptibility to schizophrenia.
Park TW; Yoon KS; Kim JH; Park WY; Hirvonen A; Kang D
Eur Neuropsychopharmacol; 2002 Aug; 12(4):299-303. PubMed ID: 12126868
[TBL] [Abstract][Full Text] [Related]
19. Influence of tumor necrosis factor alpha gene promoter polymorphisms and its serum level on migraine susceptibility in Egyptian patients.
Fawzi MS; El-Shal AS; Rashad NM; Fathy HA
J Neurol Sci; 2015 Jan; 348(1-2):74-80. PubMed ID: 25434717
[TBL] [Abstract][Full Text] [Related]
20. The A218C polymorphism of tryptophan hydroxylase gene and migraine.
Erdal N; Herken H; Yilmaz M; Erdal E; Bayazit YA
J Clin Neurosci; 2007 Mar; 14(3):249-51. PubMed ID: 17194593
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
