C. Mahasandana

发表

Hemophilia with factor VIII and factor IX inhibitors, incidence, bleeding problems and management.

C. Mahasandana, D. Patharathienskul, V. Suvatte, 1993, The Southeast Asian journal of tropical medicine and public health.

Genotype and phenotype of haemophilia A in Thai patients

P. Yenchitsomanus, C. Mahasandana, V. Akkarapatumwong, 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

Determination of haemophilia A carrier status by mutation analysis

S. Panyim, P. Yenchitsomanus, C. Mahasandana, 2001, Haemophilia : the official journal of the World Federation of Hemophilia.

Determination of haemophilia A carrier status by mutation analysis.

S. Panyim, P. Yenchitsomanus, C. Mahasandana, 2001 .

Homozygous Protein S Deficiency: 7-Year Follow-Up

C. Mahasandana, V. Suvatte, G. Veerakul, 1996, Thrombosis and Haemostasis.

Homozygous protein S deficiency in an infant with purpura fulminans.

A. Chuansumrit, M. Manco‐Johnson, C. Mahasandana, 1990, The Journal of pediatrics.

Malignancies in HIV-infected children at Siriraj Hospital.

K. Sanpakit, C. Mahasandana, G. Veerakul, 2002, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Malignant lymphoma in Thailand: changes in the frequency of malignant lymphoma determined from a histopathologic and immunophenotypic analysis of 425 cases at Siriraj Hospital

C. Mahasandana, G. Veerakul, S. Sukpanichnant, 1998, Cancer.

Malignant lymphoma in Thailand

C. Mahasandana, V. Suvatte, G. Veerakul, 1998 .

A novel Asn344 deletion in the core domain of coagulation factor XIII A subunit: its effects on protein structure and function.

G. Chelvanayagam, R. Baker, P. Yenchitsomanus, 1998, Blood.

A Novel Asn 344 Deletion in the Core Domain of Coagulation Factor XIII A Subunit : Its Effects on Protein Structure and Function

G. Chelvanayagam, R. Baker, P. Yenchitsomanus, 1998 .

Deletion in the Core Domain of Coagulation Factor XIII A Subunit : Its Effects on Protein Structure and Function

G. Chelvanayagam, R. Baker, P. Yenchitsomanus, 1998 .

Neonatal purpura fulminans associated with homozygous protein S deficiency

R. Marlar, M. Manco‐Johnson, C. Mahasandana, 1990, The Lancet.

Cord blood coagulation studies in infants of high-risk pregnant women.

E. Makowski, C. Mahasandana, W. Hathaway, 1975, American journal of obstetrics and gynecology.

Paradoxical Bleeding in Intensively Transfused Hemophiliacs: Alteration of Platelet Function

C. Mahasandana, J. Humbert, W. Hathaway, 1973, Transfusion.

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

C. Mahasandana, W. Hathaway, 1973, Pediatric Research.

Successful prophylaxis of intracranial hemorrhage in infants with severe congenital factor VII deficiency.

C. Mahasandana, V. Suvatte, G. Veerakul, 2000, The Southeast Asian journal of tropical medicine and public health.

National survey of patients with hemophilia and other congenital bleeding disorders in Thailand.

A. Chuansumrit, C. Mahasandana, P. Angchaisuksiri, 2004, The Southeast Asian journal of tropical medicine and public health.

Acquired platelet dysfunction with eosinophilia: study of platelet function in 62 cases.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1979, The Southeast Asian journal of tropical medicine and public health.

Bone marrow transplantation for thalassemia in Thailand.

C. Mahasandana, V. Suvatte, D. Chandanayingyong, 1993, Bone marrow transplantation.

Linear growth in homozygous beta-thalassemia and beta-thalassemia/hemoglobin E patients under different treatment regimens.

V. Viprakasit, C. Mahasandana, V. Suvatte, 2001, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

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

C. Mahasandana, V. Suvatte, G. Veerakul, 2000, Bone Marrow Transplantation.

Combination of chemotherapy, radiotherapy and immunotherapy for acute lymphoblastic leukemia in children.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1981, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Acquired bleeding disorders: the impact of health problems in the developing world

A. Chuansumrit, C. Mahasandana, P. Angchaisuksiri, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Glucose-6-phosphate dehydrogenase deficiency in the newborn: its prevalence and relation to neonatal jaundice.

C. Mahasandana, V. Suvatte, J. Soongswang, 1995, The Southeast Asian journal of tropical medicine and public health.

Transient, acquired glucose-6-phosphate dehydrogenase deficiency in Thai children with typhoid fever.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1982, The Southeast Asian journal of tropical medicine and public health.

Compound Heterozygosity for One Novel and One Recurrent Mutation in a Thai Patient with Severe Protein S Deficiency

R. Bertina, C. Mahasandana, V. Suvatte, 1999, Thrombosis and Haemostasis.

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

K. Sanpakit, C. Mahasandana, G. Veerakul, 2002, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Sinus histiocytosis with massive lymphadenopathy: the first three cases reported in Thailand.

C. Mahasandana, V. Suvatte, S. Sukpanichnant, 1990, Asian Pacific journal of allergy and immunology.

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

S. Duga, F. Peyvandi, C. Mahasandana, 2004, European Journal of Human Genetics.

Comparison of oral and parenteral vitamin K prophylaxis for prevention of late hemorrhagic disease of the newborn.

C. Mahasandana, G. Green, L. Jacobson, 1991, The Journal of pediatrics.

Frameshift mutations with severe and moderate clinical phenotypes in Thai hemophilia A patients

S. Panyim, P. Yenchitsomanus, C. Mahasandana, 2000, Human mutation.

Mutations of the factor VIII gene in Thai hemophilia A patients

S. Panyim, P. Yenchitsomanus, C. Mahasandana, 2000, Human mutation.

Bone marrow, peripheral blood and cord blood stem cell transplantation in children: ten years' experience at Siriraj Hospital.

C. Mahasandana, V. Suvatte, D. Chandanayingyong, 1998, International journal of hematology.

Prevalence of hemoglobin E, alpha-thalassemia and glucose-6-phosphate dehydrogenase deficiency in 1,000 cord bloods studied in Bangkok.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1995, The Southeast Asian journal of tropical medicine and public health.

Hypertension posttransfusion in Thai thalassemic children: early detection and management.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1988, Birth defects original article series.

Pyruvate kinase deficiency in an alpha-thalassemia family: first case report in Thailand.

C. Mahasandana, V. Suvatte, G. Veerakul, 1997, The Southeast Asian journal of tropical medicine and public health.