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Thromb Haemost 2002; 88(02): 370-371
DOI: 10.1055/s-0037-1613219
DOI: 10.1055/s-0037-1613219
Letters to the Editor
Perinatal Management of Patients at High Risk of Homozygous Protein C Deficiency
Further Information
Publication History
Received
26 February 2002
Accepted
03 May 2002
Publication Date:
07 December 2017 (online)
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References
- 1 Seligsohn U, Berger A, Abend M, Rubin L, Attias D, Zivelin A. et al. Homozygous protein C deficiency manifested by massive venous thrombosis in the newborn. New Engl J Med 1984; 310 (09) 559-62.
- 2 Kirkinen P, Salonvaara M, Nikolajev K, Vanninen R, Heinonen K. Antepartum findings in fetal protein C deficiency. Prenat Diagn 2000; 20 (09) 746-9.
- 3 Marlar RA, Montgomery RR, Broekmans AW. Report on the diagnosis and treatment of homozygous protein C deficiency. Report of the Working Party on Homozygous Protein C Deficiency of the ICTH-Subcommittee on Protein C and Protein S. Thromb Haemost 1989; 61 (03) 529-31.
- 4 Jerkeman A, Henriksson P, Jonsson NO, Berntorp E. [Homozygous protein C deficiency can be detected by prenatal diagnosis]. Lakartidningen 1998; 95 (36) 3772. 3775-7.
- 5 Millar DS, Allgrove J, Rodeck C, Kakkar VV, Cooper DN. A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy. Blood Coagul Fibrinolysis 1994; 05 (04) 647-9.
- 6 Reitsma PH, Bernardi F, Doig RG, Gandrille S, Greengard JS, Ireland H. et al. Protein C deficiency: a database of mutations, 1995 update. Thromb Haemost 1995; 73: 876-89.
- 7 Reverdiau-Moalic P, Delahousse B, Body G, Bardos P, Leroy J, Gruel Y. Evolution of blood coagulation activators and inhibitors in the healthy human fetus. Blood 1996; 88 (03) 900-6.