Search Results - "SIRACHAINAN, N"

Hematopoietic stem cell transplantation for homozygous β-thalassemia and β-thalassemia/hemoglobin E patients from haploidentical donors by Anurathapan, U, Hongeng, S, Pakakasama, S, Sirachainan, N, Songdej, D, Chuansumrit, A, Charoenkwan, P, Jetsrisuparb, A, Sanpakit, K, Rujkijyanont, P, Meekaewkunchorn, A, Lektrakul, Y, Iamsirirak, P, Surapolchai, P, Satayasai, W, Sirireung, S, Sruamsiri, R, Wahidiyat, P A, Ungkanont, A, Issaragrisil, S, Andersson, B S

“…Thalassemia-free survival after allogeneic stem cell transplantation (SCT) is about 80–90% with either matched-related or -unrelated donors. We explored the…”
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Successful HLA haploidentical HSCT with post-transplant cyclophosphamide in Wiskott–Aldrich syndrome by Kreetapirom, P, Hongeng, S, Manuyakorn, W, Anurathapan, U, Pakakasama, S, Sirachainan, N, Andersson, B S

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Association of factor VIII and factor IX mutations, HLA Class II, tumour necrosis factor-[alpha] and interleukin-10 on inhibitor development among Thai haemophilia A and B patients by Chuansumrit, A, Sasanakul, W, Sirachainan, N, Kadegasem, P, Wongwerawattanakoon, P, Mahaklan, L, Nathalang, O

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Association of factor VIII and factor IX mutations, HLA Class II, tumour necrosis factor‐α and interleukin‐10 on inhibitor development among Thai haemophilia A and B patients by Chuansumrit, A., Sasanakul, W., Sirachainan, N., Kadegasem, P., Wongwerawattanakoon, P., Mahaklan, L., Nathalang, O.

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Three-Decade Successive Establishment of Care for Women/Girls from Families with Haemophilia by Chuansumrit, Ampaiwan, Sasanakul, Werasak, Sirachainan, Nongnuch, Santiwatana, Suttikarn, Kadegasem, Praguywan, Wongwerawattanakoon, Pakawan, Tungbubpha, Noppawan, Chantaraamporn, Juthamard

“…Objective: The study aimed to report a 3-decade successive establishment of care for women/girls from families with haemophilia. Methods: A retrospective…”
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Prenatal diagnosis for haemophilia: the Thai experience by Chuansumrit, A., Sasanakul, W., Promsonthi, P., Sirachainan, N., Panburana, P., Kadegasem, P., Wongwerawattanakoon, P.

“…Background Haemophilia is a lifelong X‐linked recessive inherited bleeding disorder. Since the haemophilia management in economically less‐developed countries…”
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Development of a Thai version of the paediatric bleeding assessment tool (Thai paediatric‐BAT) suitable for use in children with inherited mucocutaneous bleeding disorders by Pakdeeto, S., Natesirinilkul, R., Komwilaisak, P., Rand, M. L., Blanchette, V. S., Vallibhakara, S. A., Sirachainan, N.

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Severe Nonfebrile Dengue Infection in an Adolescent After Postoperative Kidney Transplantation: A Case Report by Tangnararatchakit, K, Tirapanich, W, Tapaneya-Olarn, W, Sumethkul, V, Sirachainan, N, Watcharananan, S, Leenanupunth, C, Yoksan, S, Chuansumrit, A

“…Abstract We herein have reported a case of severe nonfebrile dengue infection complicated with refractory pancytopenia and a large perinephric hematoma with…”
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Safety and efficacy of recombinant activated factor VII for long-term secondary prophylaxis in a haemophilia boy with high-titre inhibitors by Chuansumrit, A., Sirachainan, N., Panuwannakorn, M., Wongwerawattanakoon, P., Kadegasem, P., Choeyprasert, W., Sasanakul, W.

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Simple and accurate bedside diagnostic kit for determining haemophilia A and B: a revised version by Sasanakul, W., Kadegasem, P., Chaiyaratana, W., Wongwerawattanakoon, P., Sirachainan, N., Chuansumrit, A.

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Simple multiplex RT-PCR for identifying common fusion transcripts in childhood acute leukemia by PAKAKASAMA, S., KAJANACHUMPOL, S., KANJANAPONGKUL, S., SIRACHAINAN, N., MEEKAEWKUNCHORN, A., NINGSANOND, V., HONGENG, S.

“…Summary Nonrandom gene rearrangements have been demonstrated in leukemic cells at diagnosis. These genetic abnormalities are associated with specific types,…”
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Dengue virus infection in haemophilic patients: aggravation of bleeding risk by CHUANSUMRIT, A., TANGNARARATCHAKIT, K., SIRACHAINAN, N., KHOSITSETH, A., KUPTANON, T., WANITKUN, S., WITHURAWANIT, W., SONGDEJ, D.

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Interphase-FISH screening for eight common rearrangements in pediatric B-cell precursor acute lymphoblastic leukemia by Hutspardol, S., Pakakasama, S., Kanta, K., Nuntakarn, L., Anurathapan, U., Sirachainan, N., Songdej, D., Sawangpanich, R., Tiyasirichokchai, R., Rerkamnuaychoke, B., Hongeng, S.

“…Summary Introduction This is the first pilot study to screen multiple common genetic aberrations in B‐cell precursor acute lymphoblastic leukemia (BCP‐ALL)…”
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Combined factor V and factor VIII deficiency in a Thai patient: a case report of genotype and phenotype characteristics by Sirachainan, N., Zhang, B., Chuansumrit, A., Pipe, S., Sasanakul, W., Ginsburg, D.

“…A Thai woman, with no family history of bleeding disorders, presented with excessive bleeding after minor trauma and tooth extraction. The screening…”
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Outcome of transplantation with unrelated donor bone marrow in children with severe thalassaemia by HONGENG, S, PAKAKASAMA, S, CHAISIRIPOOMKERE, W, CHUANSUMRIT, A, SIRACHAINAN, N, UNGKANONT, A, JOOTAR, S

“…We conducted a study of unrelated donor bone marrow transplantation (BMT) in 11 children with severe thalassaemia. The conditioning regimen consisted of…”
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Efficacy of different doses of recombinant activated factor VII in the treatment of haemophilia children with inhibitor by CHUANSUMRIT, A., SIRACHAINAN, N., PAKAKASAMA, S., SUEBSANGAD, A., CHOTSUPPAKARN, S., WONGWERAWATTANAKOON, P.

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Rituximab as an adjuvant therapy to immune tolerance in a haemophilia A boy with high inhibitor titre by CHUANSUMRIT, A., HUSAPADOL, S., WONGWERAWATTANAKOON, P., HONGENG, S., SIRACHAINAN, N., PAKAKASAMA, S.

“…We report a haemophilia A boy with high inhibitor titre (170 BU) who experienced five life‐threatening bleeding episodes during a one‐year period from 9 to 21…”
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Auto-immune haemolytic anaemia concurrent with Plasmodium vivax infection: a case report by Sitcharungsi, R, Anurathapan, U, Sirachainan, N, Chanthavanich, P

“…A 7-month-old Myanmar boy was admitted with a 3-day history of fever. He was markedly pale and his temperature was 38·2°C. Peripheral blood smear demonstrated…”
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Preserving eye function in prematurely born children with severe protein C deficiency by Sirachainan, N., Chuansumrit, A., Hanutsaha, P., Pakakasama, S., Hongeng, S.

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PB1077 A Novel C238G, PROC Mutation in Patients with Thromboembolism, Causes Intracellular Protein Retention by Tanratana, P., Seanoon, K., Kadegasem, P., Chuansumrit, A., Sirachainan, N.

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