نتائج البحث

Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy.

• Authors : Singha K; Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand.; Faculty of Medicine, Mahasarakham University, Mahasarakham, Thailand.

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/diagnosis ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics ; beta-Thalassemia*

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Feb 10; Vol. 17 (1), pp. 45. Date of Electronic Publication: 2022 Feb 10.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

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Trace Elements and Oxidant/Antioxidant Status in Beta-Thalassemia Patients.

• Authors : Mohammed, Ibrahim Majer¹ ; Alsalimi, Sadoun Abbas²; Al-Fartosy, Adnan Jassim Mohammed³

Subjects: *OXIDANT status; *TRACE elements; *BETA-ThalassemiaIRAQ

• Source: Bahrain Medical Bulletin. Dec2023, Vol. 45 Issue 4, p1772-1778. 7p.

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Strengthening Education to Bridge the Thalassemia Care Gap.

• Authors : Khan, Lutfunnahar¹

• Source: Journal of Bangladesh College of Physicians & Surgeons. Jan2024, Vol. 42 Issue 1, p1-3. 3p.

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Hemoglobinopathy: molecular epidemiological characteristics and health effects on Hakka people in the Meizhou region, southern China.

• Authors : Lin M; Laboratory Medical Center, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, Guangdong Province, People's Republic of China.; Wen YF

Subjects: Ethnicity*; Hemoglobinopathies/Hemoglobinopathies/Hemoglobinopathies/*epidemiology ; Hemoglobinopathies/Hemoglobinopathies/Hemoglobinopathies/*genetics

• Source: PloS one [PLoS One] 2013; Vol. 8 (2), pp. e55024. Date of Electronic Publication: 2013 Feb 01.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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In Utero Hematopoietic Stem Cell Transplantation for Alpha-thalassemia Major (ATM)

• Authors : California Institute for Regenerative Medicine (CIRM); Tippi Mackenzie, Professor of Surgery

• Source: Derderian SC, Jeanty C, Walters MC, Vichinsky E, MacKenzie TC. In utero hematopoietic cell transplantation for hemoglobinopathies. Front Pharmacol. 2015 Jan 12;5:278. doi: 10.3389/fphar.2014.00278.

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Thalassemia and hemoglobinopathy prevalence in a community-based sample in Sylhet, Bangladesh.

• Authors : Wendt, Amanda S.; Brintrup, Joaquin; Waid, Jillian L.

Subjects: HEMOGLOBINOPATHY; THALASSEMIA; BETA-ThalassemiaBANGLADESH

• Source: Orphanet Journal of Rare Diseases; 7/19/2023, Vol. 18 Issue 1, p1-11, 11p

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Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations.

• Authors : Qiu, Yuling; Wei, Shilu; Hou, Wei

Subjects: PHENOTYPES; DNA analysis; BETA-Thalassemia

• Source: Hemoglobin; Mar2023, Vol. 47 Issue 2, p52-55, 4p

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Multiplex Quantitative Real-Time Polymerase Chain Reaction and High-Resolution Melting Analysis for Identification of a Couple At-Risk of Having a Newborn with Severe Thalassemia.

• Authors : Ruengdit C; Division of Clinical Microscopy, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand.; Punyamung M

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/diagnosis ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics

• Source: Hemoglobin [Hemoglobin] 2021 Sep; Vol. 45 (5), pp. 309-313. Date of Electronic Publication: 2022 Feb 09.Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Alpha thalassemia genotypes in Kuwait.

• Authors : Adekile, Adekunle¹ (AUTHOR) ; Sukumaran, Jalaja¹ (AUTHOR); Thomas, Diana¹ (AUTHOR)

• Source: BMC Medical Genetics. 8/24/2020, Vol. 21 Issue 1, pN.PAG-N.PAG. 1p.

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The spectrum of Alpha and Beta Thalassemia Mutations: A 10-year Population-based Study of the Premarital Health Screening Program in West of Iran.

• Authors : Pooladi, Arash; Gheshlagh, Reza Ghanei; Kahrizi, Nahid

Subjects: BETA-Thalassemia; HEALTH programs; GENETIC carriersIRAN; KURDISTAN

• Source: Iranian Journal of Pediatric Hematology & Oncology; 2022, Vol. 12 Issue 3, p190-198, 9p

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