Search Results

The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population

Authors: SAID, Joanne M.; BRENNECKE, Shaun P.; MOSES, Eric K.; WALKER, Susan P.; MONAGLE, Paul T.; CAMPBELL, Janine; BRYANT, Valerie J.; BORG, Anthony J.; HIGGINS, John R.

Source: Australian and New Zealand Journal of Obstetrics and Gynaecology, Volume 48, Number 6, December 2008 , pp. 536-541(6)

Publisher: Blackwell Publishing

Paternal Thrombophilic Gene Mutations Are Not Associated with Recurrent Miscarriage

Authors: Toth, Bettina; Vocke, Franziska; Rogenhofer, Nina; Friese, Klaus; Thaler, Christian J.; Lohse, Peter

Source: American Journal of Reproductive Immunology, Volume 60, Number 4, October 2008 , pp. 325-332(8)

Publisher: Blackwell Publishing

Frequency of factor V Leiden mutation in Egyptian cases with myocardial infarction

Authors: Settin, Ahmad; Dowaidar, Moataz; El-Baz, Rizk; Abd-Al-Samad, Ayman; El-Sayed, Ibrahim; Nasr, Mahmoud

Source: Hematology, Volume 13, Number 3, June 2008 , pp. 170-174(5)

Publisher: Maney Publishing

Thrombophilic mutations in pre-eclampsia and pregnancy-induced hypertension

Authors: Omar, Siti Z.; Qvist, Rajes; Khaing, Si L.; Muniandy, Sekaran; Bhalla, Sunil

Source: The Journal of Obstetrics and Gynaecology Research, Volume 34, Number 2, April 2008 , pp. 174-178(5)

Publisher: Blackwell Publishing

Cerebral venous sinus thrombosis as a recurrent thrombotic event in a patient with heterozygous prothrombin G20210A genotype after discontinuation of oral anticoagulation therapy: How long should we treat these patients with warfarin?

Authors: Jukic, Ivana; Titlic, Marina; Tonkic, Ante; Rosenzweig, Daniel

Source: Journal of Thrombosis and Thrombolysis, Volume 24, Number 1, August 2007 , pp. 77-80(4)

Publisher: Springer

Development of a calibrated automated thrombography based thrombin generation test in mouse plasma

Authors: TCHAIKOVSKI, S. N.; VAN VLIJMEN, B. J. M.; ROSING, J.; TANS, G.

Source: Journal of Thrombosis and Haemostasis, Volume 5, Number 10, October 2007 , pp. 2079-2086(8)

Publisher: Blackwell Publishing

Frequency of selected thrombophilias in women with placental abruption

Authors: PROCHÁZKA, Martin; LUBUŠKÝ, Marek; SLAVÍK, Luděk; HRACHOVEC, Petr; ZIELINA, Petr; KUDELA, Milan; LINDQVIST, Pelle G.

Source: Australian and New Zealand Journal of Obstetrics and Gynaecology, Volume 47, Number 4, August 2007 , pp. 297-301(5)

Publisher: Blackwell Publishing

Colon cancer metastasis in mouse liver is not affected by hypercoagulability due to Factor V Leiden mutation

Authors: Klerk, C.P.W.; Smorenburg, S.M.; Spek, C.A.; Van Noorden, C.J.F.

Source: Journal of Cellular and Molecular Medicine, Volume 11, Number 3, May/June 2007 , pp. 561-568(8)

Publisher: Blackwell Publishing

Mutations in Clotting Factors and Inflammatory Bowel Disease

Authors: Bernstein, Charles N.; Sargent, Michael; Vos, Hans L.; Rosendaal, Frits R.

Source: The American Journal of Gastroenterology, Volume 102, Number 2, February 2007 , pp. 338-343(6)

Publisher: Blackwell Publishing

Screening for inherited thrombophilia might be warranted among Eastern Mediterranean sickle-ßeta-0 thalassemia patients

Authors: Isma'eel, Hussain; Arnaout, M.; Shamseddeen, Wael; Mahfouz, R.; Zeineh, N.; Jradi, Oussama; Taher, Ali

Source: Journal of Thrombosis and Thrombolysis, Volume 22, Number 2, October 2006 , pp. 121-123(3)

Publisher: Springer

ID: 263

Authors: Colucci, M.; Binetti, B.; Spiezia, L.; Gavasso, S.; Semeraro, N.; Simioni, P.

Source: Journal of Thrombosis and Haemostasis, Volume 4, Supplement 1, October 2006 , pp. 92-92(1)

Publisher: Blackwell Publishing

Purpura fulminans as a sequel to erythema nodosum in a child with homozygous Leiden mutation and acquired protein S deficiency

Authors: Foyn Bruun, Cathrine; Langbakk, Bodil; Eriksson Steigen, Sonja

Source: Acta Pædiatrica, Volume 94, Number 8, August 2005 , pp. 1155-1158(4)

Publisher: Blackwell Publishing

Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutation

Authors: BRUGGE, J. M.; SIMIONI, P.; BERNARDI, F.; TORMENE, D.; LUNGHI, B.; TANS, G.; PAGNAN, A.; ROSING, J.; CASTOLDI, E.

Source: Journal of Thrombosis and Haemostasis, Volume 3, Number 12, December 2005 , pp. 2695-2702(8)

Publisher: Blackwell Publishing

Purpura fulminans as a sequel to erythema nodosum in a child with homozygous Leiden mutation and acquired protein S deficiency

Authors: Bruun, Cathrine; Langbakk, Bodil; Eriksson Steigen, Sonja

Source: Acta Paediatrica, Volume 94, Number 8, Number 8/August 2005 , pp. 1155-1158(4)

Publisher: Informa Healthcare

The factor V Glu1608Lys mutation is recurrent in familial thrombophilia

Authors: LUNGHI, B.; SCANAVINI, D.; CASTOLDI, E.; GEMMATI, D.; TOGNAZZO, S.; REDAELLI, R.; GHIRARDUZZI, A.; IERAN, M.; PINOTTI, M.; BERNARDI, F.

Source: Journal of Thrombosis and Haemostasis, Volume 3, Number 9, September 2005 , pp. 2032-2038(7)

Publisher: Blackwell Publishing

The Role of Factor V Leiden in Maternal Health and the Outcome of Pregnancy

Authors: Calderwood, C. J.; Greer, I. A.

Source: Current Drug Targets, Volume 6, Number 5, August 2005 , pp. 567-576(10)

Publisher: Bentham Science Publishers

The prevalence of inherited thrombophilias in a Caucasian Australian population

Authors: Gibson, Catherine; MacLennan, Alastair; Rudzki, Zbigniew; Hague, William; Haan, Eric; Sharpe, Phillipa; Priest, Kevin; Chan, Annabelle; Dekker, Gustaaf; Goldwater, Paul; Khong, T. Yee; Morton, Mark; Ranieri, Enzo; Scott, Heather; Tapp, Heather; Casey, Graeme

Source: Pathology, Volume 37, Number 2, April 2005 , pp. 160-163(4)

Publisher: Informa Healthcare

Impact of environmental and hereditary risk factors on the clinical manifestation of thrombophilia in homozygous carriers of factor V:G1691A

Authors: Ehrenforth S.; Nemes L.; Mannhalter C.; Rosendaal F.R.; Koder S.; Zoghlami-Rintelen C.; Scharrer I.; Pabinger I.

Source: Journal of Thrombosis and Haemostasis, Volume 2, Number 3, March 2004 , pp. 430-436(7)

Publisher: Blackwell Publishing

Risk of venous thromboembolism during pregnancy in homozygous carriers of the factor V Leiden mutation: are there any predictive factors?

Source: Journal of Thrombosis and Haemostasis, Volume 2, Number 2, February 2004 , pp. 359-360(2)

Publisher: Blackwell Publishing

Homozygous factor V Leiden mutation in a patient with traumatic leg ulceration

Authors: Loone N.M.; Lee B.; Anderson J.; McKenna K.

Source: Clinical & Experimental Dermatology, Volume 28, Number 6, November 2003 , pp. 608-609(2)

Publisher: Blackwell Publishing