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pro vyhledávání: '"M, Wongchanchailert"'
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Publikováno v:
European journal of haematology. 67(2)
Seventy-eight patients with IVS-1 nt 5, G-C, which is the common mutation of beta+-thalassemia found in the southern part of Thailand, were studied to determine whether it is possible to predict phenotypic severity from genetic factors. The clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46c1e690c6bdaf030ff6e99ae999cf21
https://pubmed.ncbi.nlm.nih.gov/11722597
https://pubmed.ncbi.nlm.nih.gov/11722597
Publikováno v:
Haematologica. 86(2)
Frameshift 41/42 mutation is the most common mutation of beta0-thalassemia found in Thailand. We studied clinical and hematologic features in 84 patients and relatives with frameshift 41/42 to determine whether it is possible to predict phenotypic se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c940c5ca79d4d36ba50ad08bdbbf1ea2
https://pubmed.ncbi.nlm.nih.gov/11224481
https://pubmed.ncbi.nlm.nih.gov/11224481
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 83(2)
A prospective and descriptive study was carried out in 17 children with chronic ITP. Five-day course of Intraglobin (400 mg/kg/d x 5) was given intravenously to 10 children with the age of 4-16 years (5 males and 5 females). Two-day course of Venoglo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e0ff049b28da0f3cbe80a590c52d664
https://pubmed.ncbi.nlm.nih.gov/10710885
https://pubmed.ncbi.nlm.nih.gov/10710885
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 28(1)
One hundred and one thalassemic patients, 37 with homozygous beta-thalassemia, 60 with beta-thalassemia Hb E and 4 with hemoglobin H disease with Hb Constant Spring were studied. Twenty-four of 101 (23.8%) tested positive for antibody to hepatitis C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca9e0f93aba63874a1bd06b7b9ae5852
https://pubmed.ncbi.nlm.nih.gov/9322298
https://pubmed.ncbi.nlm.nih.gov/9322298
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 28
A total of 50 patients and relatives were studied comprising 12 cases of compound heterozygosity of beta-Malay and beta + thalassemia, 10 cases of compound heterozygosity of beta-Malay and beta degree thalassemia, 10 cases of beta-Malay and HbE and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c8db85efadf5b077ab6366ef32a65d7f
https://pubmed.ncbi.nlm.nih.gov/9640610
https://pubmed.ncbi.nlm.nih.gov/9640610
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 27(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::791b7c0f8381f2fe9a1f6bc8d3cde67b
https://pubmed.ncbi.nlm.nih.gov/9280014
https://pubmed.ncbi.nlm.nih.gov/9280014
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 76(5)
Acarboxy prothrombin or PIVKA-II (protein induced by vitamin K absence or antagonist-II) was used to determine the presence of vitamin deficiency in newborn infants. Of 230 cord blood samples assayed by using ELISA method, 34.8 per cent were positive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3cc06d46791f81cfabc576d78d6a68a6
https://pubmed.ncbi.nlm.nih.gov/8006559
https://pubmed.ncbi.nlm.nih.gov/8006559
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 23
Spontaneous platelet aggregation was studied in 51 children and adolescents, comprising 30 nonsplenectomized thalassemic patients, 12 splenectomized thalassemic patients and 9 normal children. Spontaneous platelet aggregation was significantly increa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::45a2705e2dc6c941db1db89c60a8d935
https://pubmed.ncbi.nlm.nih.gov/1298992
https://pubmed.ncbi.nlm.nih.gov/1298992
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 73(12)
A 14-year-old boy with Langerhans cell histiocytosis of the spinal cord who presented with progressive enlarged bilateral inguinal masses, difficulty in urination, walking and paresthesia in the left lower extremity and perineum is reported. Radiogra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b4c5bd6195810c8b213866780733c15
https://pubmed.ncbi.nlm.nih.gov/2086719
https://pubmed.ncbi.nlm.nih.gov/2086719