C Mahasandana

Homozygous protein S deficiency in an infant with purpura fulminans

C Mahasandana, V Suvatte, Ampaiwan Chuansumrit et al. · The Journal of Pediatrics · 1990 · 95 citations

Developmental Biology, Genetic Disorder, Genetics +6

Secondary hemophagocytic lymphohistiocytosis in children: an analysis of etiology and outcome.

Gavivann Veerakul, Kleebsabai Sanpakit, Voravarn S. Tanphaichitr et al. · PubMed · 2002 · 72 citations

Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aα-chain gene

Silvia Spena, Stefano Duga, Rosanna Asselta et al. · European Journal of Human Genetics · 2004 · 69 citations · Full text

Congenital Afibrinogenaemia, Developmental Biology, Genetic Disorder +4

Successful bone marrow transplantation in a child with red blood cell pyruvate kinase deficiency

VS Tanphaichitr, V Suvatte, Surapol Issaragrisil et al. · Bone Marrow Transplantation · 2000 · 54 citations

Transplantation, Marrow Transplantation, Bone Marrow Failure +8

Circulating Anticoagulants in the Newborn: Relation to Hypercoagulability and the Idiopathic Respiratory Distress Syndrome

C Mahasandana, William E. Hathaway · Pediatric Research · 1973 · 49 citations · Full text

Thrombosis, Hematology, Pediatrics +6