Graves' disease associated with anticardiolipin antibody positivity and acquired protein S deficiencyNAKAYAMA, Tomohiro; YAMAMOTO, Tatsuo; KANMATSUSE, Katsuo et al.Rheumatology international (Berlin. Print). 2003, Vol 23, Num 4, pp 198-200, issn 0172-8172, 3 p.Article

Genotype and Laboratory and Clinical Phenotypes of Protein S DeficiencyDUEBGEN, Sebastian; KAUKE, Teresa; MARSCHALL, Christoph et al.American journal of clinical pathology. 2012, Vol 137, Num 2, pp 178-184, issn 0002-9173, 7 p.Article

Functional characterization of twelve natural PROS1 mutations associated with anticoagulant protein S deficiencyHURTADO, Begona; MUNOZ, Xavier; CARME MULERO, Maria et al.Haematologica (Roma). 2008, Vol 93, Num 4, pp 574-580, issn 0390-6078, 7 p.Article

Large deletions of the PROSI gene in a large fraction of mutation- negative patients with protein S deficiencyJOHANSSON, Anna M; HILLARP, Andreas; SÄLL, Torbjörn et al.Thrombosis and haemostasis. 2005, Vol 94, Num 5, pp 951-957, issn 0340-6245, 7 p.Article

The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general populationBEAUCHAMP, Nicholas J; DYKES, Anne C; PARIKH, Nirzari et al.British journal of haematology. 2004, Vol 125, Num 5, pp 647-654, issn 0007-1048, 8 p.Article

A large deletion of the PROSI gene in a deep vein thrombosis patient with protein S deficiencyTONG YIN; TAKESHITA, Satoshi; SAKATA, Yoichi et al.Thrombosis and haemostasis. 2007, Vol 98, Num 4, pp 783-789, issn 0340-6245, 7 p.Article

Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA)YOO, Jong-Ha; KIM, Hee-Jin; MAENG, Ho-Young et al.Thrombosis research. 2009, Vol 123, Num 5, pp 793-795, issn 0049-3848, 3 p.Article

Normal functional protein S activity does not exclude protein S deficiencyRODGER, Marc A; CARRIER, Marc; GERVAIS, Muriel et al.Pathophysiology of haemostasis and thrombosis (Print). 2003, Vol 33, Num 4, pp 202-205, issn 1424-8832, 4 p.Article

First case of protein S deficiency due to a translocation t(3;21)(q11.2;q22)HURTADO, Begona; NADAL, Marga; MARGARIT, Ester et al.Thrombosis and haemostasis. 2009, Vol 101, Num 5, pp 977-979, issn 0340-6245, 3 p.Article

Protein S abnormalities: a diagnostic nightmareMARLAR, Richard A; GAUSMAN, Jana N.American journal of hematology. 2011, Vol 86, Num 5, pp 418-421, issn 0361-8609, 4 p.Article

Thrombose des sinus veineux endocrâniens et déficit acquis en antithrombine, protéines C et S au cours d'une chimiothérapie : observation clinique chez un jeune patient = Cerebral sinovenous thrombosis and acquired antithrombin, protein C and S deficiency during chemotherapy in a young man : report of a caseTERRONES MUNOZ, V; TRIFFET, A; CAUCHIE, P et al.Revue médicale de Bruxelles. 2008, Vol 29, Num 6, pp 535-539, issn 0035-3639, 5 p.Article

A Rare Splicing Mutation in the PROS1 Gene of a Korean Patient with Type I Hereditary Protein S DeficiencyCHOI, Jonghyeon; KIM, Hee-Jin; MYUNG HEE CHANG et al.Annals of clinical and laboratory science. 2011, Vol 41, Num 4, pp 397-400, issn 0091-7370, 4 p.Article

Mid-dermal elastolysis with prothrombotic abnormalities: two casesOZZANI, E. C; SANTORO, F; PARODI, A et al.British journal of dermatology (1951). 2009, Vol 161, Num 1, pp 203-205, issn 0007-0963, 3 p.Article

POSTINFECTIOUS PURPURA FULMINANS SECONDARY TO VARICELLA-INDUCED PROTEIN S DEFICIENCYJANUARIO, Gustavo; RAMROOP, Shiva; SHINGADIA, Delane V et al.The Pediatric infectious disease journal. 2010, Vol 29, Num 10, pp 981-983, issn 0891-3668, 3 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

Regulation of coagulation by protein SCASTOLDI, Elisabetta; HACKENG, Tilman M.Current opinion in hematology. 2008, Vol 15, Num 5, pp 529-536, issn 1065-6251, 8 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

Severe protein S deficiency associated with heterozygous factor V Leiden mutation in a child with purpura fulminansDOGAN, Yasar; AYGUN, Denizmen; YILMAZ, Yelda et al.Pediatric hematology and oncology. 2003, Vol 20, Num 1, pp 1-5, issn 0888-0018, 5 p.Article

High risk of pregnancy-related venous thromboembolism in women with multiple thrombophilic defectsFOLKERINGA, Nienke; BROUWER, Jan Leendert P; KORTEWEG, Fleurisca J et al.British journal of haematology. 2007, Vol 138, Num 1, pp 110-116, issn 0007-1048, 7 p.Article

Portal vein thrombosis in a patient with hiv treated with a protease inhibitor-containing regimenSOENTJENS, P; OSTYN, B; VAN OUTRYVE, S et al.Acta Clinica Belgica. 2006, Vol 61, Num 1, pp 24-29, issn 0001-5512, 6 p.Article

Protein S deficiency with a PROS1 gene mutation in a patient presenting with mesenteric venous thrombosis following total colectomyJI, Misuk; SANG NAM YOON; LEE, Woochang et al.Blood coagulation & fibrinolysis. 2011, Vol 22, Num 7, pp 619-621, issn 0957-5235, 3 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

Risk Factors for Venous Thromboembolism in Patients with Human Immunodeficiency Virus InfectionKISER, Katie L; BADOWSKI, Melissa E.Pharmacotherapy. 2010, Vol 30, Num 12, pp 1292-1302, issn 0277-0008, 11 p.Article

Acquired protein S deficiency leads to obliterative portal venopathy and to compensatory nodular regenerative hyperplasia in HIV-infected patientsMALLET, Vincent O; VARTHAMAN, Aditi; LASNE, Dominique et al.AIDS (London). 2009, Vol 23, Num 12, pp 1511-1518, issn 0269-9370, 8 p.Article