Zobrazeno 1 - 10
of 133
pro vyhledávání: '"C, Mahasandana"'
Autor:
V, Viprakasit, V S, Tanphaichitr, C, Mahasandana, A, Assteerawatt, L, Suwantol, G, Veerakul, S, Kankirawatana, P, Pung-Amritt, V, Suvatte
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 84(7)
The effects on linear growth and development among thalassemic patients under different treatment regimens were compared. Twelve homozygous beta-thalassemia (homozygous beta-thal) and 36 beta-thalassemia/Hb E (beta-thal/Hb E) were studied longitudina
Autor:
S, Kankirawatana, C, Mahasandana, G, Veerakul, J, Seeloem, L, Suwantol, V, Tanphaichitr, V, Suvatte
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 31(4)
During the period 1984-1992, 2 severe cases (1 male, 1 female) of congenital F VII deficiency with intracranial hemorrhage (ICH) were referred to the Department of Pediatrics, Siriraj Hospital Bangkok, Thailand at the ages of 1 and 3 months old. They
Autor:
V S, Tanphaichitr, V, Suvatte, C, Mahasandana, P, Sachapong, G, Veerakul, S, Kankirawatana, P, Wasant
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 30
Gaucher's disease, a lysosomal disorder, is not a common disease in Thailand. During the period 1966-1998 we saw 20 patients with Gaucher's disease at the Department of Pediatrics. Siriraj Hospital. The patients came from different regions of the cou
Autor:
P, Pung-amritt, S R, Poort, H L, Vos, R M, Bertina, C, Mahasandana, V S, Tanphaichitr, G, Veerakul, S, Kankirawatana, V, Suvatte
Publikováno v:
Thrombosis and haemostasis. 81(2)
Homozygous or compound heterozygous protein S (PS) deficiency is a very rare disorder in the anticoagulant system, that can lead to life-threatening thrombotic complications shortly after birth. This report describes the results of the genetic analys
Autor:
V, Suvatte, V S, Tanphaichitr, S, Visuthisakchai, C, Mahasandana, G, Veerakul, V, Chongkolwatana, D, Chandanayingyong, S, Issaragrisil
Publikováno v:
International journal of hematology. 68(4)
Stem cell transplantations were performed in 69 children at Siriraj Hospital over a ten year period. The source of stem cells was bone marrow (60), peripheral blood (3), or cord blood (6). The diseases treated included 35 thalassemias, 11 Burkitt's l
Autor:
V S, Tanphaichitr, V, Suvatte, C, Mahasandana, G, Veerakul, P, Pung-amritt, K, Tachavanich, H, Ideguchi
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 28
In Thailand, the most common cause of chronic hemolytic anemia is thalassemia hemoglobinopathy. We report here a 10-year-old girl with pyruvate kinase (PK) deficiency who was initially diagnosed to have Hb H disease, like her sister. The patient had
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 26
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is prevalent in Thailand. This condition can cause acute hemolysis during oxidative stress and also severe hyperbilirubinemia in the newborn in some populations. Our aim was to study the prevalence
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 24
The prevalence of vitamin K deficiency in the newborns delivered at Siriraj Hospital was studied. The prolongation of one stage prothrombin time and the presence of PIVKA-II (non carboxylated prothrombin antigen) in cord blood were interpreted as the
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 24
Among 117 cases of hemophilia, there were 7 hemophilia A and 2 hemophilia B with factor VIII and factor IX inhibitors diagnosed at the Department of Pediatrics, Siriraj Hospital, Bangkok, Thailand. The overall incidence of hemophilia with inhibitors
Autor:
S, Issaragrisil, S, Visudhisakchai, V, Suvatte, D, Chandanayingyong, A, Piankijagum, C, Mahasandana, V S, Tanphaichitr
Publikováno v:
Bone marrow transplantation. 12
We report our experience of bone marrow transplantation for thalassemia in Thailand. From July 1988 to September 1992, 10 thalassemic patients underwent allogeneic bone marrow transplantation. Two of them were homozygous beta-thalassemia and 8 were b