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Items: 1 to 20 of 113

1.

Atypical timing and presentation of periventricular haemorrhagic infarction in preterm infants: the role of thrombophilia.

Harteman JC, Groenendaal F, van Haastert IC, Liem KD, Stroink H, Bierings MB, Huisman A, de Vries LS.

Dev Med Child Neurol. 2012 Feb;54(2):140-7. doi: 10.1111/j.1469-8749.2011.04135.x. Epub 2011 Nov 18.

2.

Thrombophilic polymorphisms--factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations--and preterm birth.

Resch B, Gallistl S, Kutschera J, Mannhalter C, Muntean W, Mueller WD.

Wien Klin Wochenschr. 2004 Sep 30;116(17-18):622-6.

PMID:
15515881
3.

Neuroimaging and neurodevelopmental outcome of preterm infants with a periventricular haemorrhagic infarction located in the temporal or frontal lobe.

Soltirovska Salamon A, Groenendaal F, van Haastert IC, Rademaker KJ, Benders MJ, Koopman C, de Vries LS.

Dev Med Child Neurol. 2014 Jun;56(6):547-55. doi: 10.1111/dmcn.12393. Epub 2014 Feb 10.

4.

Patterns of placental pathology in preterm infants with a periventricular haemorrhagic infarction: association with time of onset and clinical presentation.

Harteman JC, Nikkels PG, Kwee A, Groenendaal F, de Vries LS.

Placenta. 2012 Oct;33(10):839-44. doi: 10.1016/j.placenta.2012.06.014. Epub 2012 Jul 25.

PMID:
22835681
5.

Absence of association of thrombophilia polymorphisms with intrauterine growth restriction.

Infante-Rivard C, Rivard GE, Yotov WV, Génin E, Guiguet M, Weinberg C, Gauthier R, Feoli-Fonseca JC.

N Engl J Med. 2002 Jul 4;347(1):19-25.

6.

Inherited thrombophilia in childhood arterial stroke: data from Lebanon.

Muwakkit SA, Majdalani M, Hourani R, Mahfouz RA, Otrock ZK, Bilalian C, Chan AK, Abboud M, Mikati MA.

Pediatr Neurol. 2011 Sep;45(3):155-8. doi: 10.1016/j.pediatrneurol.2011.03.002.

PMID:
21824561
7.
8.
9.

Effects of inherited thrombophilia in women with recurrent pregnancy loss.

Habibovic Z, Zeybek B, Sanhal C, Eroglu Z, Karaca E, Ulukus M.

Clin Exp Obstet Gynecol. 2011;38(4):347-50.

PMID:
22268272
10.

Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.

Rahimi Z, Nomani H, Mozafari H, Vaisi-Raygani A, Madani H, Malek-Khosravi S, Parsian A.

Blood Coagul Fibrinolysis. 2009 Jun;20(4):252-6. doi: 10.1097/MBC.0b013e3283255487.

PMID:
19349859
11.

Cerebral venous and sinus thrombosis and thrombophilic mutations in Western Iran: association with factor V Leiden.

Rahimi Z, Mozafari H, Bigvand AH, Doulabi RM, Vaisi-Raygani A, Afshari D, Razazian N, Rezaei M.

Clin Appl Thromb Hemost. 2010 Aug;16(4):430-4. doi: 10.1177/1076029609335519. Epub 2009 Aug 23.

PMID:
19703820
12.

Thrombophilic polymorphisms in preterm delivery.

Valdez LL, Quintero A, Garcia E, Olivares N, Celis A, Rivas F Jr, Rivas F.

Blood Cells Mol Dis. 2004 Jul-Aug;33(1):51-6.

PMID:
15223011
13.

Thrombophilia and immunological disorders in pregnancies as risk factors for small for gestational age infants.

Verspyck E, Le Cam-Duchez V, Goffinet F, Tron F, Marpeau L, Borg JY.

BJOG. 2002 Jan;109(1):28-33.

14.

Inherited thrombophilia polymorphisms and pregnancy outcomes in nulliparous women.

Said JM, Higgins JR, Moses EK, Walker SP, Borg AJ, Monagle PT, Brennecke SP.

Obstet Gynecol. 2010 Jan;115(1):5-13. doi: 10.1097/AOG.0b013e3181c68907.

PMID:
20027027
15.

Relationship between preterm labor and thrombophilic gene polymorphism: A prospective sequential cohort study.

Uvuz F, Kilic S, Yilmaz N, Tuncay G, Cakar E, Yuksel B, Bilge U.

Gynecol Obstet Invest. 2009;68(4):234-8. doi: 10.1159/000237743. Epub 2009 Sep 17.

PMID:
19776610
16.

Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults.

Voetsch B, Damasceno BP, Camargo EC, Massaro A, Bacheschi LA, Scaff M, Annichino-Bizzacchi JM, Arruda VR.

Thromb Haemost. 2000 Feb;83(2):229-33.

PMID:
10739378
17.

[Risk of thrombophilia in carriers of thrombophilic genetic factors in unsuccessful assisted reproduction].

Ivanov P, Komsa-Penkova R, Kovacheva K, Konova E, Todorova K, Simeonova M, Ivanov I, Stoĭkov S, Popov I, Tanchev S, Bozhinova S.

Akush Ginekol (Sofiia). 2007;46(6):3-8. Bulgarian.

PMID:
17974163
18.

Combined inherited thrombophilia and adverse pregnancy outcome.

Androutsopoulos G, Mougiou A, Karakantza M, Sakellaropoulos G, Kourounis G, Decavalas G.

Clin Exp Obstet Gynecol. 2007;34(4):236-8.

PMID:
18225686
19.

Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.

Yasa MH, Bolaman Z, Yukselen V, Kadikoylu G, Karaoglul AO, Batun S.

Hepatogastroenterology. 2007 Jul-Aug;54(77):1438-42.

PMID:
17708272
20.

[Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].

Kovacheva K, Ivanov P, Konova E, Simeonova M, Komsa-Penkova R.

Akush Ginekol (Sofiia). 2007;46(7):10-6. Bulgarian.

PMID:
18333414

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