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2. [Homozygous infant in a family with hereditary protein C deficiency]. Hintz G; Weil J; Buchmann S; Azzam A; Auberger K; Beck C Klin Wochenschr; 1987 Jul; 65(12):576-80. PubMed ID: 3626426 [TBL] [Abstract][Full Text] [Related]
3. Homozygous protein C deficiency with delayed onset of symptoms at 7 to 10 months. Tuddenham EG; Takase T; Thomas AE; Awidi AS; Madanat FF; Abu Hajir MM; Kernoff PB; Hoffbrand AV Thromb Res; 1989 Mar; 53(5):475-84. PubMed ID: 2660320 [TBL] [Abstract][Full Text] [Related]
4. Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family. Cafolla A; D'Andrea G; Baldacci E; Margaglione M; Mazzucconi MG; Foà R Eur J Haematol; 2012 Apr; 88(4):336-9. PubMed ID: 22168450 [TBL] [Abstract][Full Text] [Related]
5. "Pseudo homozygous" activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds. Simioni P; Scudeller A; Radossi P; Gavasso S; Girolami B; Tormene D; Girolami A Thromb Haemost; 1996 Mar; 75(3):422-6. PubMed ID: 8701401 [TBL] [Abstract][Full Text] [Related]
6. Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group. Ireland H; Thompson E; Lane DA Thromb Haemost; 1996 Dec; 76(6):867-73. PubMed ID: 8972002 [TBL] [Abstract][Full Text] [Related]
7. Adult-onset arterial thrombosis in a pedigree of homozygous and heterozygous protein C deficiency. Tajima K; Yamamoto H; Yamamoto M; Kato Y; Kato T Thromb Res; 2013 Jan; 131(1):102-4. PubMed ID: 23174622 [No Abstract] [Full Text] [Related]
8. Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T). Song KS; Park YS; Choi CR; Kim HK; Park Q; Kim HS J Korean Med Sci; 1998 Apr; 13(2):186-90. PubMed ID: 9610620 [TBL] [Abstract][Full Text] [Related]
9. Homozygous protein C deficiency with moderately severe clinical symptoms. Sharon C; Tirindelli MC; Mannucci PM; Tripodi A; Mariani G Thromb Res; 1986 Feb; 41(4):483-8. PubMed ID: 3754354 [TBL] [Abstract][Full Text] [Related]
10. Homozygous protein C deficiency manifested by massive venous thrombosis in the newborn. Seligsohn U; Berger A; Abend M; Rubin L; Attias D; Zivelin A; Rapaport SI N Engl J Med; 1984 Mar; 310(9):559-62. PubMed ID: 6546411 [TBL] [Abstract][Full Text] [Related]
11. Dysfunctional protein C deficiency (type II). A report of 11 cases in 3 American families and review of the literature. Berdeaux DH; Abshire TC; Marlar RA Am J Clin Pathol; 1993 Jun; 99(6):677-86. PubMed ID: 8322701 [TBL] [Abstract][Full Text] [Related]
12. Paediatric presentation and outcome of congenital protein C deficiency in Japan. Ohga S; Kang D; Kinjo T; Ochiai M; Doi T; Ishimura M; Kayamori Y; Urata M; Yamamoto J; Suenobu SI; Kanegane H; Ikenoue T; Shirahata A; Hara T Haemophilia; 2013 May; 19(3):378-84. PubMed ID: 23379934 [TBL] [Abstract][Full Text] [Related]
13. [Protein C deficiency and vascular thromboses. Apropos of 2 cases and a review of the literature]. Debrueres-Gris S; Lekieffre J; Werquin S; Kacet S; Jude B Arch Mal Coeur Vaiss; 1989; 82(8):1459-65. PubMed ID: 2508600 [TBL] [Abstract][Full Text] [Related]
14. Beta 2-glycoprotein I deficiency and the risk of thrombosis. Bancsi LF; van der Linden IK; Bertina RM Thromb Haemost; 1992 Jun; 67(6):649-53. PubMed ID: 1509404 [TBL] [Abstract][Full Text] [Related]
15. Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis. Tjeldhorn L; Sandset PM; Haugbro K; Skretting G Thromb Res; 2010 Mar; 125(3):230-4. PubMed ID: 19535131 [TBL] [Abstract][Full Text] [Related]
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17. Antithrombin III deficiency. Cucuianu M; Blaga S; Pop S; Olinic D; Olinic N; Colhon D; Cristea A Rom J Intern Med; 1994; 32(2):119-27. PubMed ID: 7920326 [TBL] [Abstract][Full Text] [Related]
18. Familial thrombophilia and the prothrombin 20210A mutation: association with increased thrombin generation and unusual thrombosis. Eikelboom JW; Ivey L; Ivey J; Baker RI Blood Coagul Fibrinolysis; 1999 Jan; 10(1):1-5. PubMed ID: 10070829 [TBL] [Abstract][Full Text] [Related]
19. Two cases of inherited triple deficiency in a large kindred with thrombotic diathesis and deficiencies of antithrombin III, heparin cofactor II, protein C and protein S. Jobin F; Vu L; Lessard M Thromb Haemost; 1991 Sep; 66(3):295-9. PubMed ID: 1836072 [TBL] [Abstract][Full Text] [Related]
20. Severe inherited "homozygous" protein C deficiency in a newborn infant. Estellés A; Garcia-Plaza I; Dasí A; Aznar J; Duart M; Sanz G; Pérez-Requejo JL; España F; Jimenez C; Abeledo G Thromb Haemost; 1984 Aug; 52(1):53-6. PubMed ID: 6548587 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]