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Thromb Haemost 1996; 76(06): 1122
DOI: 10.1055/s-0038-1650718
Original Article
Schattauer GmbH Stuttgart

Homozygous Protein S Deficiency: 7-Year Follow-Up

Chularatana Mahasandana
The Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand
,
Gavivann Veerakul
The Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand
,
Voravam S Tanphaichitr
The Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand
,
Vinai Suvatte
The Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand
,
Nisarat Opartkiattikul
2   The Clinical Pathology, Siriraj Hospital, Mahidol University, Bangkok, Thailand
,
William E Hathaway
1   The University of Colorado School of Medicine, Denver, Colorado, USA
› Author Affiliations
Further Information

Publication History

Received 15 December 1995

Accepted after resubmission 20 August 1996

Publication Date:
11 July 2018 (online)

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  • References

  • 1 Mahasandana C, Suvatte V, Chuansumrit A. et al Homozygous protein S deficiency in an infant with purpura fulminans. J Pediatr 1990; 117: 750-753
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  • 2 Comp PC, Doray D, Patton D, Esmon CT. An abnormal plasma distribution of protein S occurs in functional protein S deficiency. Blood 1988; 67: 504-508
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  • 3 Koike Y, Sumi Y, Wakabayashi K, Ichikawa Y. The monoclonal antibody to human protein S that inhibits the binding of protein S to C4b-binding protein. Thromb Haemost 1989 62. Abstract No. 875
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