Homozygous Protein S Deficiency: 7-Year Follow-Up

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Thromb Haemost 1996; 76(06): 1122
DOI: 10.1055/s-0038-1650718

Original Article

Schattauer GmbH Stuttgart

Autoren

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

²The Clinical Pathology, Siriraj Hospital, Mahidol University, Bangkok, Thailand
William E Hathaway

¹The University of Colorado School of Medicine, Denver, Colorado, USA

Received 15. Dezember 1995

Accepted after resubmission 20. August 1996

Publikationsdatum:
11. Juli 2018 (online)

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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