Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Mahasandana C"'
Publikováno v:
Haemophilia. Oct2004 Supplement 4, Vol. 10, p188-195. 8p.
Autor:
Varaporn Akkarapatumwong, S. Oranwiroon, P. Thanootarakul, Mahasandana C, Pa-thai Yenchitsomanus, Parichat Pung-Amritt, Sorasak Intorasoot, Gavivann Veerakul
Publikováno v:
Haemophilia. 9:179-186
Summary. To study genotype and phenotype correlation of haemophilia A in Thai patients, molecular defects of the factor VIII (FVIII) gene were examined and their correlation with clinical phenotypes were evaluated. The molecular pathologies of FVIII
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb17656a350015e49131873ba9448fc5
https://doi.org/10.1046/j.1365-2516.2003.00729.x
https://doi.org/10.1046/j.1365-2516.2003.00729.x
Autor:
S. Oranwiroon, Mahasandana C, Parichat Pung-Amritt, Varaporn Akkarapatumwong, P. Thanootarakul, Gavivann Veerakul, Pa-thai Yenchitsomanus
Publikováno v:
Haemophilia. 7:335-338
A splicing defect with 201 nucleotide deletion in the factor VIII transcript due to IVS15 + 1G > T mutation inactivating this donor splice site and activating a cryptic acceptor splice site in exon 16 was identified in a severe haemophilia A patient.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a1da58418770a4cb57aab24fc3e3d62
https://doi.org/10.1046/j.1365-2516.2001.00507.x
https://doi.org/10.1046/j.1365-2516.2001.00507.x
Autor:
Varaporn Akkarapatumwong, Sakol Panyim, Gavivann Veerakul, Mahasandana C, Pa-thai Yenchitsomanus, Parichat Pung-Amritt, S. Oranwiroon, Ajjima Treesucon
Publikováno v:
Haemophilia. 7:20-25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5541c4da5a64b708ae78ac0b0f8b7fc8
https://doi.org/10.1111/j.1365-2516.2001.00453.x
https://doi.org/10.1111/j.1365-2516.2001.00453.x
Autor:
Parichat Pung-Amritt, Mahasandana C, Varaporn Akkarapatumwong, Ajjima Treesucon, S. Oranwiroon, Pa-thai Yenchitsomanus, Gavivann Veerakul, Sakol Panyim
Publikováno v:
Haemophilia. 7:20-25
A reliable method for determination of carrier status and genetic counselling is required for effective control of haemophilia. Linkage analysis is currently the most widely used method for this purpose; however, in cases where there is no prior fami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c68208b43b731ea3e5ee8bd57d2826b
https://doi.org/10.1046/j.1365-2516.2001.00453.x
https://doi.org/10.1046/j.1365-2516.2001.00453.x
Autor:
Parichat Pung-Amritt, S R Poort, Mahasandana C, Gavivann Veerakul, Hans L. Vos, Vinai Suvatte, Rogier M. Bertina, Voravarn S. Tanphaichitr, Suthida Kankirawatana
Publikováno v:
Thrombosis and Haemostasis. 81:189-192
SummaryHomozygous 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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d1fae311513d8e4099a72a8a0caefb3
https://doi.org/10.1055/s-0037-1614440
https://doi.org/10.1055/s-0037-1614440
Autor:
Wanchai Wanachiwanawin, Gavivann Veerakul, Anong Piankijagum, Sanya Sukpanichnant, Mahasandana C, D Sonakul, Vinai Suvatte, Voravarn S. Tanphaichitr
Publikováno v:
Cancer. 83:1197-1204
BACKGROUND Analysis of malignant lymphoma in a single institution at different periods of time can determine the changing status of the disease in the region. METHODS To compare with the large series of 1095 lymphoma cases reported between 1957-1971
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::909ae102210c7c06350066d6bf0815b8
https://doi.org/10.1002/(sici)1097-0142(19980915)83:6<1197::aid-cncr20>3.0.co
https://doi.org/10.1002/(sici)1097-0142(19980915)83:6<1197::aid-cncr20>3.0.co
Autor:
Parichat Pung-Amritt, Rohan T. Baker, Philip G. Board, Pa-thai Yenchitsomanus, Mahasandana C, Sasichai Kangsadalampai, Gareth Chelvanayagam
Publikováno v:
Blood. 92:481-487
In this study a previously undescribed 3 bp deletion, AAT1030-1032, in the factor XIII A subunit gene, has been detected in a Thai patient. The inframe deletion results in the translation of a factor XIII A subunit that lacks Asn344. This is the firs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67c54572b02618467c2e149b129d0945
https://doi.org/10.1182/blood.v92.2.481.413a33_481_487
https://doi.org/10.1182/blood.v92.2.481.413a33_481_487
Autor:
P. Pung-Amritt, Linda J. Jacobson, P. Pintadit, P.B. Isarangkura, William E. Hathaway, G.M. Green, Mahasandana C
Publikováno v:
The Journal of Pediatrics. 119:461-464
4. Ascher DP, Wilson S, Fischer GW. Comparison of bacteremia and antigen detection in a neonatal group B streptococcal sepsis model [Abstract 1602]. Society for Pediatric Research. Anaheim, Calif., May 6-11, 1990. 5. Harris MC, Deuber C, Polin RA, et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::befdc4cdcecaa8267821a7473bc62d6f
https://doi.org/10.1016/s0022-3476(05)82064-5
https://doi.org/10.1016/s0022-3476(05)82064-5
Autor:
Ampaiwan Chuansumrit, William E. Hathaway, Mahasandana C, Richard A. Mariar, Linda J. Jacobson, Marilyn J. Manco-Johnson, Vinai Suvatte
Publikováno v:
The Journal of Pediatrics. 117:750-753
Protein C, a vitamin K--dependent zymogen, and its cofactor, protein S (also vitamin K dependent), play major roles in the anticoagulant system for limiting thrombus formation.I, 2 Deficiency of either protein C or S is associated with recurrent fami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44e6887c24083c3ffef351d84c84da79
https://doi.org/10.1016/s0022-3476(05)83335-9
https://doi.org/10.1016/s0022-3476(05)83335-9