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Benign intracranial hypertension associated to blood coagulation derangements.

De Lucia D, Napolitano M, Di Micco P, Niglio A, Fontanella A, Di lorio G.

Thromb J. 2006 Dec 24;4:21.PMID: 17187688 [PubMed]Related articlesFree article

Potentially prothrombotic abnormalities of coagulation in benign intracranial hypertension.

Sussman J, Leach M, Greaves M, Malia R, Davies-Jones GA.

J Neurol Neurosurg Psychiatry. 1997 Mar;62(3):229-33.PMID: 9069476 [PubMed - indexed for MEDLINE]Related articlesFree article

Analysis of inherited thrombophilic mutations and natural anticoagulant deficiency in patients with idiopathic portal hypertension.

Bayan K, Tüzün Y, Yilmaz S, Canoruc N, Dursun M.

J Thromb Thrombolysis. 2009 Jul;28(1):57-62. Epub 2008 Aug 7.PMID: 18685811 [PubMed - indexed for MEDLINE]Related articles

Prothrombotic factors and the risk of acute onset non-cardioembolic stroke in young Asian Indians.

Biswas A, Ranjan R, Meena A, Akhter S, Sharma V, Yadav BK, Behari M, Saxena R.

Thromb Res. 2009 Sep;124(4):397-402. Epub 2009 Jun 27.PMID: 19560187 [PubMed - indexed for MEDLINE]Related articles

Thrombophilia and unexplained pregnancy loss in Indian patients.

Vora S, Shetty S, Salvi V, Satoskar P, Ghosh K.

Natl Med J India. 2008 May-Jun;21(3):116-9.PMID: 19004141 [PubMed - indexed for MEDLINE]Related articles

Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis.

Coulam CB, Wallis D, Weinstein J, DasGupta DS, Jeyendran RS.

Am J Reprod Immunol. 2008 Nov;60(5):426-31.PMID: 18803625 [PubMed - indexed for MEDLINE]Related articles

Prevalence of methylenetetrahydrofolate gene (MTHFR) C677T polymorphism among chronic hemodialysis patients and its association with cardiovascular disease: a cross-sectional analysis.

Ibrahim S, El Dessokiy O.

Clin Exp Nephrol. 2009 Oct;13(5):501-7. Epub 2009 May 26.PMID: 19466593 [PubMed - indexed for MEDLINE]Related articles

Plasminogen Activator Inhibitor-1 (PAI-1) Gene 4G/5G Promoter Polymorphism is Seen in Higher Frequency in the Indian Patients With Deep Vein Thrombosis.

Akhter M, Biswas A, Ranjan R, Meena A, Yadav B, Sharma A, Saxena R.

Clin Appl Thromb Hemost. 2009 May 5. [Epub ahead of print]PMID: 19419975 [PubMed - as supplied by publisher]Related articles

[Benign intracranial hypertension and heterozygosity for factor V Leiden mutation]

Pérez Martínez A, Cerezo Bueno MJ, García Peñas JJ, Gutiérrez-Solana L, Ruiz-Falcó ML.

An Pediatr (Barc). 2005 Aug;63(2):172-4. Spanish. Erratum in: An Pediatr (Barc). 2005 Sep;63(3):291. PMID: 16045879 [PubMed - indexed for MEDLINE]Related articlesFree article

A-G-4G haplotype of PAI-1 gene polymorphisms -844 G/A, HindIII G/C, and -675 4G/5G is associated with increased risk of ischemic stroke caused by small vessel disease.

Adamski MG, Turaj W, Slowik A, Wloch-Kopec D, Wolkow P, Szczudlik A.

Acta Neurol Scand. 2009 Aug;120(2):94-100. Epub 2008 Dec 22.PMID: 19154538 [PubMed - indexed for MEDLINE]Related articles

Blood coagulation and fibrinolysis in male patients with hypogonadotropic hypogonadism: plasma factor V and factor X activities increase in hypogonadotropic hypogonadism.

Erem C, Kocak M, Hacihasanoglu A, Yilmaz M.

J Endocrinol Invest. 2008 Jun;31(6):537-41.PMID: 18591887 [PubMed - indexed for MEDLINE]Related articles

Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden.

Rahimi Z, Vaisi-Raygani A, Nagel RL, Muniz A.

J Thromb Thrombolysis. 2008 Jun;25(3):288-92. Epub 2007 Jul 11.PMID: 17619828 [PubMed - indexed for MEDLINE]Related articles

The frequency of anticardiolipin antibodies and genetic mutations associated with hypercoagulability among patients with Wegener's granulomatosis with and without history of a thrombotic event.

Sebastian JK, Voetsch B, Stone JH, Romay-Penabad Z, Lo GH, Allen NB, Davis JC Jr, Hoffman GS, McCune WJ, St Clair EW, Specks U, Spiera R, Loscalzo J, Pierangeli S, Merkel PA; Wegener's Granulomatosis Etanercept Trial Research Group.

J Rheumatol. 2007 Dec;34(12):2446-50. Epub 2007 Oct 1.PMID: 17918782 [PubMed - indexed for MEDLINE]Related articles

Prothrombotic mutations as risk factors for cryptogenic ischemic cerebrovascular events in young subjects with patent foramen ovale.

Botto N, Spadoni I, Giusti S, Ait-Ali L, Sicari R, Andreassi MG.

Stroke. 2007 Jul;38(7):2070-3. Epub 2007 May 24.PMID: 17525392 [PubMed - indexed for MEDLINE]Related articlesFree article

Major and potential prothrombotic genotypes in patients with venous thrombosis and in healthy subjects from Slovenia.

Bedencic M, Bozic M, Peternel P, Stegnar M.

Pathophysiol Haemost Thromb. 2008;36(2):58-63. Epub 2009 Jan 5.PMID: 19127083 [PubMed - indexed for MEDLINE]Related articles

Genetic and acquired prothrombotic risk factors and sudden hearing loss.

Capaccio P, Ottaviani F, Cuccarini V, Bottero A, Schindler A, Cesana BM, Censuales S, Pignataro L.

Laryngoscope. 2007 Mar;117(3):547-51.PMID: 17334320 [PubMed - indexed for MEDLINE]Related articles

Angiotensin-converting enzyme D/I and plasminogen activator inhibitor-1 4G/5G gene polymorphisms are associated with increased risk of spontaneous abortions in polycystic ovarian syndrome.

Sun L, Lv H, Wei W, Zhang D, Guan Y.

J Endocrinol Invest. 2009 Jul 28. [Epub ahead of print]PMID: 19636212 [PubMed - as supplied by publisher]Related articles

Association of PAI-1 4G/5G and -844G/A gene polymorphism and changes in PAI-1/tPA levels in stroke: a case-control study.

Saidi S, Slamia LB, Mahjoub T, Ammou SB, Almawi WY.

J Stroke Cerebrovasc Dis. 2007 Jul-Aug;16(4):153-9.PMID: 17689411 [PubMed - indexed for MEDLINE]Related articles

Placental histomorphology in unexplained foetal loss with thrombophilia.

Vora S, Shetty S, Khare M, Ghosh K.

Indian J Med Res. 2009 Feb;129(2):144-9.PMID: 19293440 [PubMed - indexed for MEDLINE]Related articlesFree article

Connection between genetically determined blood coagulation factors and haemorheology.

Pongrácz E, Andrikovics H, Bernát IS, Nagy Z.

Clin Hemorheol Microcirc. 2008;39(1-4):333-41.PMID: 18503143 [PubMed - indexed for MEDLINE]Related articles