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

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

Weitere Informationen

Publikationsverlauf

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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