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kw.\*:("antithrombin deficiency")

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A novel splice-site mutation c.42-2A>T (IVS1-2A>T) of SERPINC1 in a Korean family with inherited antithrombin deficiencyMOON JU JANG; LEE, Jeong-Guil; SO YOUNG CHONG et al.Blood coagulation & fibrinolysis. 2011, Vol 22, Num 8, pp 742-745, issn 0957-5235, 4 p.Article

Changes in antithrombin activity and platelet counts in the late stage of twin and triplet pregnanciesMORIKAWA, Mamoru; YAMADA, Takashi; KATAOKA, Soromon et al.Seminars in thrombosis and hemostasis. 2005, Vol 31, Num 3, pp 290-296, issn 0094-6176, 7 p.Article

Two successful pregnancies following eight miscarriages in a patient with antithrombin deficiencySZILAGYI, A; NAGY, A; TAMAS, P et al.Gynecologic and obstetric investigation. 2006, Vol 61, Num 2, pp 111-114, issn 0378-7346, 4 p.Article

The association of inherited thrombophilia and intrauterine fetal death: a case-control studyHELGADOTTIR, Linda B; SKJELDESTAD, Finn E; JACOBSEN, Anne F et al.Blood coagulation & fibrinolysis. 2011, Vol 22, Num 8, pp 651-656, issn 0957-5235, 6 p.Article

Life-threatening thrombosis in mice with targeted Arg48-to-cys mutation of the heparin-binding domain of antithrombinDEWERCHIN, Mieke; HERAULT, Jean-Pascal; HERBERT, Jean-Marc et al.Circulation research. 2003, Vol 93, Num 11, pp 1120-1126, issn 0009-7330, 7 p.Article

Reduction of high fetal loss rate by anticoagulant treatment during pregnancy in antithrombin, protein C or protein S deficient womenFOLKERINGA, Nienke; BROUWER, Jan Leendert P; KORTEWEG, Fleurisca J et al.British journal of haematology. 2007, Vol 136, Num 4, pp 656-661, issn 0007-1048, 6 p.Article

The risk of recurrent venous thromboembolism in patients with inherited deficiency of natural anticoagulants antithrombin, protein C and protein SDE STEFANO, Valerio; SIMIONI, Paolo; ROSSI, Elena et al.Haematologica (Roma). 2006, Vol 91, Num 5, pp 695-698, issn 0390-6078, 4 p.Article

Use of Subcutaneous Lepirudin in an Obese Surgical Intensive Care Unit Patient with Heparin ResistanceINMAN, Kristin R; GERLACH, Anthony T.The Annals of pharmacotherapy. 2009, Vol 43, Num 10, pp 1714-1718, issn 1060-0280, 5 p.Article

Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort studyKUMAR, Riten; CHAN, Anthony K. C; DAWSON, Jennifer E et al.British journal of haematology. 2014, Vol 166, Num 1, pp 130-139, issn 0007-1048, 10 p.Article

Hereditary Deficiency of Protein C or Protein S Confers Increased Risk of Arterial Thromboembolic Events at a Young Age : Results From a Large Family Cohort StudyMAHMOODI, Bakhtawar K; BROUWER, Jan-Leendert P; VEEGER, Nic J. G. M et al.Circulation (New York, N.Y.). 2008, Vol 118, Num 16, pp 1659-1667, issn 0009-7322, 9 p.Article

The risk of symptomatic pulmonary embolism due to proximal deep venous thrombosis differs in patients with different types of inherited thrombophiliaROSSI, Elena; ZA, Tommaso; CIMINELLO, Angela et al.Thrombosis and haemostasis. 2008, Vol 99, Num 6, pp 1030-1034, issn 0340-6245, 5 p.Article

Role of antithrombin concentrate in treatment of hereditary antithrombin deficiency : An updateRODGERS, George M.Thrombosis and haemostasis. 2009, Vol 101, Num 5, pp 806-812, issn 0340-6245, 7 p.Article

Neuraxial anesthesia for labor and cesarean delivery in a parturient with hereditary antithrombin deficiency on recombinant human antithrombin infusion therapyPAMNANI, Anup; ROSENSTEIN, Megan; DARWICH, Alaeldin et al.Journal of clinical anesthesia. 2010, Vol 22, Num 6, pp 450-453, issn 0952-8180, 4 p.Article

Molecular basis of antithrombin deficiencyLUXEMBOURG, Beate; DELEV, Daniel; LINDHOFF-LAST, Edelgard et al.Thrombosis and haemostasis. 2011, Vol 105, Num 4, pp 635-646, issn 0340-6245, 12 p.Article

Antithrombin Krakow II (c.624+1 G > T): a novel mutation leading to type 1 antithrombin deficiencyCELINSKA-LÖWENHOFF, Magdalena; LWANIEC, Teresa; ALHENC-GELAS, Martine et al.Blood coagulation & fibrinolysis. 2012, Vol 23, Num 5, pp 454-455, issn 0957-5235, 2 p.Article

Antithrombin alfa in hereditary antithrombin deficient patients : A phase 3 study of prophylactic intravenous administration in high risk situationsTIEDE, Andreas; CAMPBELL TAIT, R; SCHULMAN, Sam et al.Thrombosis and haemostasis. 2008, Vol 99, Num 3, pp 616-622, issn 0340-6245, 7 p.Article

Gestational thrombocytopenia and pregnancy-induced antithrombin deficiency: Progenitors to the development of the HELLP syndrome and acute fatty liver of pregnancyMINAKAMI, Hisanori; YAMADA, Hideto; SUZUKI, Shigenori et al.Seminars in thrombosis and hemostasis. 2002, Vol 28, Num 6, pp 515-518, issn 0094-6176, 4 p.Article

Clinical and laboratory characteristics of paediatric and adolescent index cases with venous thromboembolism and antithrombin deficiency: An observational multicentre cohort studyLIMPERGER, Verena; FRANKE, Andre; KNOEFLER, Ralf et al.Thrombosis and haemostasis. 2014, Vol 112, Num 3, pp 478-485, issn 0340-6245, 8 p.Article

Molecular mechanisms of antithrombin deficiency in two Chinese families : One novel and one recurrent point mutation in the antithrombin gene causing venous thrombosisZHOU, Rong-Fu; FU, Qi-Hua; WANG, Wen-Bin et al.Thrombosis and haemostasis. 2005, Vol 94, Num 6, pp 1172-1176, issn 0340-6245, 5 p.Article

Usefulness of antithrombin deficiency phenotypes for risk assessment of venous thromboembolism: type I deficiency as a strong risk factor for venous thromboembolismMITSUGURO, Mana; SAKATA, Toshiyuki; OKAMOTO, Akira et al.International journal of hematology. 2010, Vol 92, Num 3, pp 468-473, issn 0925-5710, 6 p.Article

Impact of the type of SERPINC1 mutation and subtype of antithrombin deficiency on the thrombotic phenotype in hereditary antithrombin deficiencyLUXEMBOURG, Beate; PAVLOVA, Anna; GEISEN, Christof et al.Thrombosis and haemostasis. 2014, Vol 111, Num 2, pp 249-257, issn 0340-6245, 9 p.Article

Inherited antithrombin deficiency and pregnancy: Maternal and fetal outcomesSABADELL, Jordi; CASELLAS, Manel; ALIJOTAS-REIG, Jaume et al.European journal of obstetrics, gynecology, and reproductive biology. 2010, Vol 149, Num 1, pp 47-51, issn 0301-2115, 5 p.Article

Argatroban Anticoagulation in Renal Dysfunction : A Literature AnalysisHURSTING, Marcie J; MURRAY, Patrick T.The Nephron journals. 2008, Vol 109, Num 2, issn 1660-8151, c80-c94Article

Identification of a novel amino acid deletion mutation and a very rare single nucleotide variant in a Japanese family with type I antithrombin deficiencyKATAYAMA, Kan; HASHIMOTO, Natsuko; IMANAKA, Tsuneo et al.Thrombosis research. 2005, Vol 116, Num 3, pp 215-221, issn 0049-3848, 7 p.Article

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