Search Results

Screening and Diagnosis of Rare Thalassemia Variants.

• Authors : Haishen Tang; Yi Xiong; Jiaqi Tang

Subjects: THALASSEMIA diagnosis; RESEARCH funding; ALPHA-Thalassemia

• Source: Archives of Pathology & Laboratory Medicine. Jan2025, Vol. 149 Issue 1, pe1-e10. 10p.

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CRISPR in Public Health: The Health Equity Implications and Role of Community in Gene-Editing Research and Applications.

• Authors : Subica, Andrew M.

Subjects: GENETIC disorder treatment; PUBLIC health surveillance; GENOME editing

• Source: American Journal of Public Health. Aug2023, Vol. 113 Issue 8, p874-882. 9p.

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Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease.

• Authors : Ferraresi, Marta (AUTHOR); Panzieri, Daniele Lello (AUTHOR); Leoni, Simona (AUTHOR)

Subjects: UNITED States. Food & Drug Administration; SICKLE cell anemia; YOUNG adults

• Source: European Journal of Pediatrics. Jun2023, Vol. 182 Issue 6, p2509-2519. 11p. 1 Diagram, 3 Charts.

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Diagnosis of α0-thalassemia Chiang Rai (‐‐CR) deletion by melt curve analysis in Northern Thailand.

• Authors : Ruengdit, Chedtapak (AUTHOR); Khamphikham, Pinyaphat (AUTHOR); Punyamung, Manoo (AUTHOR)

Subjects: HYDROPS fetalis; MELTING; CURVESTHAILAND

• Source: Scandinavian Journal of Clinical & Laboratory Investigation. May2022, Vol. 82 Issue 3, p181-184. 4p.

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Hemoglobinopathy gone astray-three novel forms of α-thalassemia in Norwegian patients characterized by quantitative real-time PCR and DNA sequencing.

• Authors : Grimholt, Runa M.; Fjeld, Bente; Klingenberg, Olav

Subjects: HEMOGLOBINOPATHY; THALASSEMIA; GLOBIN genesNORWAY

• Source: Scandinavian Journal of Clinical & Laboratory Investigation. Dec 2021, Vol. 81 Issue 8, p670-678. 9p.

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The effect of food and nutrients on iron overload: what do we know so far?

• Authors : Omena, Juliana (AUTHOR); Curioni, Cíntia (AUTHOR); Cople-Rodrigues, Cláudia dos Santos (AUTHOR)

• Source: European Journal of Clinical Nutrition. Dec2021, Vol. 75 Issue 12, p1771-1780. 10p.

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Can the supplementary consumption of baobab (Adansonia digitata L.) fruit pulp improve the hemoglobin levels and iron status of schoolchildren in Kenya? Findings of a randomized controlled intervention trial.

• Authors : Evang, Esther Charlotte; Habte, Tsige-Yohannes; Owino, Willis Omondi

Subjects: MEDICINAL plants; HEMOGLOBINS; BEVERAGESKENYA

• Source: European Journal of Nutrition. Aug2021, Vol. 60 Issue 5, p2617-2629. 13p. 1 Color Photograph, 1 Diagram, 7 Charts, 2 Graphs.

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Genetic variation patterns of β-thalassemia in Western Andalusia (Spain) reveal a structure of specific mutations within the Iberian Peninsula.

• Authors : Sánchez-Martínez, Luis J. (AUTHOR); Hernández, Candela L. (AUTHOR); Rodríguez, Juan N. (AUTHOR)

Subjects: GENETIC variation; GENETIC drift; REPRODUCTIVE isolationANDALUSIA (Spain); IBERIAN Peninsula; SPAIN

• Source: Annals of Human Biology. Aug 2021, Vol. 48 Issue 5, p406-417. 12p.

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Successful four-factor preimplantation genetic testing: α- and β-thalassemia, human leukocyte antigen typing, and aneuploidy screening.

• Authors : Chen, Dongjia (AUTHOR); Shen, Xiaoting (AUTHOR); Xu, Yan (AUTHOR)

Subjects: HLA histocompatibility antigens; GENETIC testing; HEMATOPOIETIC stem cell transplantation

• Source: Systems Biology in Reproductive Medicine. Apr2021, Vol. 67 Issue 2, p151-159. 9p.

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Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand.

• Authors : Jomoui, Wittaya; Tepakhan, Wanicha; Satthakarn, Surada

Subjects: MOLECULAR spectra; GENETIC mutation; NUCLEOTIDE sequencing

• Source: Scandinavian Journal of Clinical & Laboratory Investigation. Nov2020, Vol. 80 Issue 7, p528-535. 8p.

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