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Thromb Haemost 2000; 84(05): 929-930
DOI: 10.1055/s-0037-1614146
DOI: 10.1055/s-0037-1614146
Letters to the Editor
Severe Acquired Functional Protein S Deficiency and Skin Necrosis in a Patient with ANCA-associated Vasculitis
Further Information
Publication History
Received
21 March 2000
Accepted after revision
31 May 2000
Publication Date:
13 December 2017 (online)
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References
- 1 Marlar RA, Neuman A. Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies. Sem Thromb Haemost 1990; 16: 299-309.
- 2 Sallah S, Abdallah JM, Gagnon GA. Recurrent warfarin-induced skin necrosis in kindreds with protein S deficiency. Haemostasis 1998; 28: 25-30.
- 3 Alessi MC, Aillaud MF, Boyer-Neumann C, Viard L, Camboulives J, Man-Vague I. Thromb Haemost. 1993; 69: 524-6.
- 4 Bergmann F, Hoyer PF, D’Angelo SV, Mazzola G, Oestereich C, Barthels M, D’Angelo A. Severe autoimmune protein S deficiency in a boy with idiopathic purpura fulminans. Br J Haematol 1995; 89: 610-4.
- 5 Piette WW. The differential diagnosis of purpura from a morphologic perspective. Adv Dermatol 1994; 09: 3-23.