Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Gavivann Veerakul"'
Publikováno v:
Siriraj Medical Journal, Vol 59, Iss 4 (2007)
Externí odkaz:
https://doaj.org/article/a35b6a9d01374dcc986170aaed25ff44
Publikováno v:
Siriraj Medical Journal, Vol 55, Iss 5 (2003)
Langerhans cell histiocytosis is an uncommon disease. There are various skin manifestations of this disorder. We report a 15 year-old patient with Langerhams cell histiocytosis, who first presented with polyuria, polydipsia and right elbow pain. A fe
Externí odkaz:
https://doaj.org/article/29e0e0b179714f8596cbe0e4822ee7f3
Autor:
Suthida Kankirawatana, Vinai Suvatte, Chularatana Mahasandana, Voravarn S. Tanphaichitr, Gavivann Veerakul, Vip Viprakasit
Publikováno v:
Siriraj Medical Journal, Vol 51, Iss 3 (1999)
We carried out a retrospective analysis of the outcome of treatment in patients with severe aplastic anemia who attended the Department of Pediatrics, Siriraj Hospital, during 1972- 1998. There were 31 patients, 17 boys and 14 girls, by Camittaâ€
Externí odkaz:
https://doaj.org/article/7c8db68c95064ba4afeefce360abf240
Autor:
Darin Sosothikul, Samart Pakakasama, Nattee Narkbunnam, Gavivann Veerakul, Su On Chainansamit, Somjai Kanjanapongkul, Surapon Wiangnon, Pattra Thanarattanakorn, Vichai Laosombat, Somporn Wangruangsathit, Rachata Lumkul
Publikováno v:
International Journal of Hematology. 91:850-854
Survivors of childhood acute lymphoblastic leukemia (ALL) are at risk of long-term late effects. Therefore, systematic screenings of the late complications are essential. The objective of this study was to determine the prevalence of late effects of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34773a58cc5c14916b009360e2d247cf
https://doi.org/10.1007/s12185-010-0594-9
https://doi.org/10.1007/s12185-010-0594-9
Autor:
Carlos A. Leal, Ira J. Dunkel, Gavivann Veerakul, Aurora Medina-Sanson, Guillermo L. Chantada, Christopher B O Yu, Mark J. Greenwald, Judith E. Kingston, John L. Hungerford, Mathew W. Wilson, Regina Wieland, Barret G. Haik, Célia Beatriz Gianotti Antoneli, Norbert Bornfeld, Amy C. Schefler, David H. Abramson, Dan S. Gombos
Publikováno v:
Ophthalmology. 114:1378-1383
Purpose To describe a series of patients with secondary acute myelogenous leukemia (sAML) and retinoblastoma (RB). Design Retrospective observational cases series. Participants Ocular and pediatric oncologists at referral centers in Europe and the Am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3317d476ed5a0e708274316f002b4dde
https://doi.org/10.1016/j.ophtha.2007.03.074
https://doi.org/10.1016/j.ophtha.2007.03.074
Autor:
Su-on Chainansamit, Surapon Wiangnon, Somjai Kanjanapongkul, Thirachit Chotsampancharoen, Gavivann Veerakul, Panya Seksarn
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 16(11)
BACKGROUND In recent decades, the prognosis for childhood leukemia has improved, especially for acute lymphoblastic leukemia (ALL). In Thailand, though, the survival rate for ALL is unimpressive. In 2006, standard national protocols for childhood leu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38f73574171d849d3a7638799ef25ac3
https://pubmed.ncbi.nlm.nih.gov/26107212
https://pubmed.ncbi.nlm.nih.gov/26107212
Autor:
Voravarn S. Tanphaichitr, Bunchoo Pongtanakul, Kleebsabai Sanpakit, Gavivann Veerakul, Worrawut Chinchang, Vip Viprakasit
Publikováno v:
Annals of Tropical Paediatrics. 24:323-328
Acute haemolysis associated with mild upper respiratory tract infection was observed in a Thai boy who presented with a rapid decline in haemoglobin (Hb) levels, haemoglobinuria and evidence of intravascular haemolysis. Several possible causes giving
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aaee36b2ea7ba691e80fc60ac6a4d6e
https://doi.org/10.1179/027249304225019145
https://doi.org/10.1179/027249304225019145
Autor:
Vip Viprakasit, Gavivann Veerakul, Voravarn S. Tanphaichitr, Panutsaya Tientadakul, Kleebsabai Sanpakit
Publikováno v:
Journal of Pediatric Hematology/Oncology. 25:261-265
Secondary polycythemia caused by high-oxygen-affinity hemoglobin is rare in children. Most patients with this condition have asymptomatic erythrocytosis. In this article the authors describe a young boy from Thailand with plethora, hypoxemia, and agg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aff33ae11976e15367ca70c9bc6c7ca9
https://doi.org/10.1097/00043426-200303000-00016
https://doi.org/10.1097/00043426-200303000-00016
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