Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Sumalee, Jindadamrongwech"'
Autor:
Parin Kamseng, Objoon Trachoo, Paisan Jittorntam, Bhakbhoom Panthan, Winai Wananukul, Sumalee Jindadamrongwech, Pimjai Niparuck, Walaiporn Yimniam, Satariya Trakulsrichai, Pitsucha Sanguanwit
Publikováno v:
Hematology. 22:114-118
To investigate the cause(s) of a Thai male proband presenting low oxygen saturation by pulse oximetry (SpOAs Hb variant was suspected, Hb typing was determined by high-performance liquid chromatography and capillary electrophoresis, and subsequently
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c40ee592fa8b45e1708c0248b6adde3a
https://doi.org/10.1080/10245332.2016.1231989
https://doi.org/10.1080/10245332.2016.1231989
Publikováno v:
Journal of Clinical Laboratory Analysis. 30:633-640
Background Definitive detection of hemoglobin (Hb) variants requires DNA sequencing. High-resolution melting (HRM) analysis of polymerase chain reaction (PCR) amplicons was applied to detect and discriminate among uncommon α-Hb variants found in Tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b58b1b205a89374b0e8c1fbe7dc4a23
https://doi.org/10.1002/jcla.21914
https://doi.org/10.1002/jcla.21914
Publikováno v:
Hemoglobin. 41(4-6)
Thalassemias and glucose-6-phosphate dehydrogenase (G6PD) deficiency are the most common inherited blood disorders. They are distributed among populations living in malaria endemic regions resulting in survival advantage from severe malaria disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e92943a3fce9f2b85ca9acc5f434e88f
https://pubmed.ncbi.nlm.nih.gov/29251006
https://pubmed.ncbi.nlm.nih.gov/29251006
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 47(1)
Genetic factors influencing Hb F content in adult red blood cells include β-thalassemia genotypes, co-inheritance of α-thalassemia traits and single nucleotide polymorphisms (SNPs). Genotyping of α- and β-thalassemia and five SNPs in β-globin ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2d911a3bcbc743782742717423e54269
https://pubmed.ncbi.nlm.nih.gov/27086429
https://pubmed.ncbi.nlm.nih.gov/27086429
Publikováno v:
Hemoglobin. 36:293-298
A rare nondeletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai boy with Hb H (β4) disease. The proband has α-thal-1 (- -(SEA) type) together with a non productive Hb Queens Park (HBA1:c.98TA) [α32(B13)Met→Lys] α1-globin varia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8aa35de886c4575a0117464d8aa9aec
https://doi.org/10.3109/03630269.2012.658939
https://doi.org/10.3109/03630269.2012.658939
Publikováno v:
Hemoglobin. 36:200-204
A large deletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai woman with Hb H disease. The proband has α-thal-1 (SEA type) in conjunction with a 16.6 kb deletion affecting the α2-globin allele. The proband had severe anemia and re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09ac6243596b9994a18e4d151bc4e6ce
https://doi.org/10.3109/03630269.2012.655355
https://doi.org/10.3109/03630269.2012.655355
Publikováno v:
Hemoglobin. 34:161-164
The S-window hemoglobin (Hb) variants revealed by high performance liquid chromatography (HPLC) were studied in 12 Thai individuals. The variants were identified, using DNA sequencing and multiplex amplification refractory mutation system-polymerase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::342c9af85f85ad22225d606c4f861a26
https://doi.org/10.3109/03630261003679631
https://doi.org/10.3109/03630261003679631
Publikováno v:
Hemoglobin. 39(3)
Laboratory investigation of hemoglobinopathies includes complete blood count (CBC), hemoglobin (Hb) typing by high performance liquid chromatography (HPLC) and DNA analysis. DNA analysis is the most reliable method but requires a manually laborious p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05322adf71cdd3469e201defd3b710a0
https://pubmed.ncbi.nlm.nih.gov/26016900
https://pubmed.ncbi.nlm.nih.gov/26016900
Autor:
Yoshiyuki Suzuki, Sumalee Jindadamrongwech, Lars O. Magnius, Helene Norder, Mohammad Mehaboob Hussain, Luisa Imberti, Shigenobu Kawai, Chetan Datta Poduri, Betty H. Robertson, Fumitaka Suzuki, Osamu Yokosuka, Efraín Garrido, Yasuo Hirai, Yasuji Arase, Vicente Soriano, Elba D. Carrillo, Shinichi Hino, Srinivasan Krishnan, Pierre Coursaget, Salvatore Casari, Mariko Kobayashi, Hiromitsu Saisho, Giampiero di Gennaro, Ettore Bidoli, Stephen Locarnini, Rosamaria Tedeschi, Michio Kimura, Nobuaki Gotou, Madhavi Chandra, Nafeesa Farees, M D'Andrea, Kenji Ikeda, Stefania Zanussi, Maria Teresa Bortolin, Giampiero Carosi, Fumio Imazeki, Hiromitsu Kumada, Hitomi Sezaki, Guntaka Venkata Ramareddy, Akira Hayasaka, Norio Akuta, Paolo De Paoli, Shosuke Iwama, Chiara Pratesi, Silvia Pirovano, Mohammad Nanne Khaja, Masahiro Kobayashi, Noriaki Suzuki, Kenichi Fukai, C M Habibullah, Tatsuo Kanda, Francesca Moretti, Patricio Gariglio, Darron R. Brown, Mohammad Aejaz Habeeb, Motohide Takashi, Eugenia Quiros-Roldan, José M. Echevarría, Carlo Torti, Katsuo Uchiumi, Elizabeth E. Lehr, Isa K. Mushahwar, Akihito Tsubota, Shou-Dong Lee, Anne-Marie Couroucé, Satoshi Saitoh, Takashi Someya, Calla R. Brown, Tetsuya Hosaka, Duncan R. Smith
Publikováno v:
Intervirology. 47:310-313
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87ee4aa1d46dcec06ff9f0bdf30a9bee
https://doi.org/10.1159/000080873
https://doi.org/10.1159/000080873
Autor:
Wansa Banyatsuppasin, Sonnarong Pounsawat, Sumalee Jindadamrongwech, Kobkorn Pongjantharasatien
Publikováno v:
Hemoglobin. 40:283-284
α-Thalassemia (α-thal) is one of the most common genetic diseases in Thailand. Homozygosity of α-thal-1 (- -/- -) and compound heterozygosity of α-thal-1/α-thal-2 (- -/-α) leads to Hb Bart's (γ4) hydrops fetalis and Hb H (β4) disease, respect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e063e1d1b2eb105a80fa7a6e52ddcbcf
https://doi.org/10.1080/03630269.2016.1189932
https://doi.org/10.1080/03630269.2016.1189932