Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Thalassemia syndrome"'
Autor:
Kritsada Singha, Supawadee Yamsri, Attawut Chaibunruang, Hataichanok Srivorakun, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Background To evaluate whether the quantification of fetal hemoglobin (Hb) Bart’s is useful for differentiation of α-thalassemia syndromes in the fetus and to characterize the fetal anemia associated with fetal α-hemoglobinopathy. Method
Externí odkaz:
https://doaj.org/article/a0e818dba38e45cba005fe6b1ba74a5e
Publikováno v:
Iraqi Journal of Hematology, Vol 11, Iss 1, Pp 13-18 (2022)
BACKGROUND: Anemia of β thalassemia results from a combination of ineffective erythropoiesis and hemolysis. This stimulates erythropoietin (EPO) production, which causes expansion of the bone marrow and may lead to serious deformities of the skull a
Externí odkaz:
https://doaj.org/article/6886bcba17a1437b9a12b71e1c2d267d
Autor:
Sudigdo Sastroasmoro, Deddy Ria Saputra, Bambang Madiyono, Ismet N. Oesman, Sukman Tulus Putra
Publikováno v:
Paediatrica Indonesiana, Vol 35, Iss 5-6, Pp 132-40 (2018)
We compared the diagnostic accuracy of electrocardiographic (ECG) criteria for left ventricular hypertrophy (LVH) in 119 randomly selected from 400 patients with thalassemia major treated at the Department of Child Health, Medical School, University
Externí odkaz:
https://doaj.org/article/26d00393ba7b47049ca9c85a5ddaf782
Publikováno v:
IP Journal of Diagnostic Pathology and Oncology. 3:118-122
Introduction: Beta Thalassemia syndrome is a group of hereditary disorders characterized by genetic deficiency in the synthesis of beta globin chains located on chromosome 11. A major diagnostic challenge is to differentiate between mild microcytic h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58e7121ac3c93887b0691ca47a40f7f1
https://doi.org/10.18231/2581-3706.2018.0025
https://doi.org/10.18231/2581-3706.2018.0025
Akademický článek
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Publikováno v:
INDIAN JOURNAL OF APPLIED RESEARCH. :23-25
Background: Hemoglobinopathies are one of the major health burden globally including India and Southeast Asian region. This study was carried out to nd out the prevalence of β-thalassemia, HbS, HbD, HbE as well as identication of asymptomatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::beee1152aa0074aa1ff75320093149ed
https://doi.org/10.36106/ijsr/1608252
https://doi.org/10.36106/ijsr/1608252
Publikováno v:
Archaeological and Anthropological Sciences. 13
The study of thalassaemia syndromes in archeological human remains is of growing interest in the field of paleopathology. However, a definitive diagnosis of the disease in skeletonized individuals remains difficult. Several non-specific bone lesions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ebb9cbc56940a154ab33d83657e9acf
https://doi.org/10.1007/s12520-020-01261-5
https://doi.org/10.1007/s12520-020-01261-5
Autor:
Kritsada Singha, Supawadee Yamsri, Attawut Chaibunruang, Hataichanok Srivorakun, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Background To evaluate whether the quantification of fetal hemoglobin (Hb) Bart’s is useful for differentiation of α-thalassemia syndromes in the fetus and to characterize the fetal anemia associated with fetal α-hemoglobinopathy. Methods A total
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1743f18240f54afea402859dbca366
https://pubmed.ncbi.nlm.nih.gov/35144630
https://pubmed.ncbi.nlm.nih.gov/35144630
Autor:
Bambang Madiyono, Deddy Ria Saputra, Sukman Tulus Putra, Ismet N. Oesman, Sudigdo Sastroasmoro
Publikováno v:
Paediatrica Indonesiana, Vol 35, Iss 5-6, Pp 132-40 (2018)
We compared the diagnostic accuracy of electrocardiographic (ECG) criteria for left ventricular hypertrophy (LVH) in 119 randomly selected from 400 patients with thalassemia major treated at the Department of Child Health, Medical School, University
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94cdcfb6632f01ca2d1c4825b10fbdf6
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/1995
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/1995
Autor:
Sanaul Haque Mia, Rustam Ali, Farid Hossain, Laila Shamima Sharmin, Khalilur Rahman, Iqbal Bari
Publikováno v:
TAJ: Journal of Teachers Association. 31:6-11
Background: Thalassemia is a common hematological disorder in our country having wide spectrum of clinical presentation. The frequency and severity of the several types of thalassemia depend on the racial background of the population. Hb-E Beta thala
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04ba5ef490cd5a6c74a8d75d07676282
https://doi.org/10.3329/taj.v31i2.41582
https://doi.org/10.3329/taj.v31i2.41582