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Quoted phrase not found in phrase index: "Alpha trait thalassemia"
Page 1
Alpha and beta thalassemia.
Muncie HL Jr, Campbell J. Muncie HL Jr, et al. Am Fam Physician. 2009 Aug 15;80(4):339-44. Am Fam Physician. 2009. PMID: 19678601 Free article. Review.
Alpha thalassemia is caused by reduced or absent synthesis of alpha globin chains, and beta thalassemia is caused by reduced or absent synthesis of beta globin chains. Imbalances of globin chains cause hemolysis and impair erythropoiesis. Silent carrie …
Alpha thalassemia is caused by reduced or absent synthesis of alpha globin chains, and beta thalassemia is cause …
Alpha-thalassaemia.
Harteveld CL, Higgs DR. Harteveld CL, et al. Orphanet J Rare Dis. 2010 May 28;5:13. doi: 10.1186/1750-1172-5-13. Orphanet J Rare Dis. 2010. PMID: 20507641 Free PMC article. Review.
Molecular analysis is usually required to confirm the haematological observations (especially in silent alpha-thalassaemia and alpha-thalassaemia trait). The predominant features in HbH disease are anaemia with variable amounts of HbH (0.8-40%). …
Molecular analysis is usually required to confirm the haematological observations (especially in silent alpha-thalassaemia and …
Alpha- and Beta-thalassemia: Rapid Evidence Review.
Baird DC, Batten SH, Sparks SK. Baird DC, et al. Am Fam Physician. 2022 Mar 1;105(3):272-280. Am Fam Physician. 2022. PMID: 35289581 Free article.
Thalassemia is a group of autosomal recessive hemoglobinopathies affecting the production of normal alpha- or beta-globin chains that comprise hemoglobin. ...Thalassemia is generally asymptomatic in trait and carrier states. Alpha-thalassemia …
Thalassemia is a group of autosomal recessive hemoglobinopathies affecting the production of normal alpha- or beta-globin chai …
The hemoglobinopathies, molecular disease mechanisms and diagnostics.
Harteveld CL, Achour A, Arkesteijn SJG, Ter Huurne J, Verschuren M, Bhagwandien-Bisoen S, Schaap R, Vijfhuizen L, El Idrissi H, Koopmann TT. Harteveld CL, et al. Int J Lab Hematol. 2022 Sep;44 Suppl 1(Suppl 1):28-36. doi: 10.1111/ijlh.13885. Int J Lab Hematol. 2022. PMID: 36074711 Free PMC article. Review.
This review summarizes the basic requirements for adequate carrier screening analysis, the importance of genotype-phenotype correlation and how this may lead to the unrevealing exceptional interactions causing a clinically more severe phenotype in otherwise asymptomatic carriers. …
This review summarizes the basic requirements for adequate carrier screening analysis, the importance of genotype-phenotype correlation and …
Optimal strategies for carrier screening and prenatal diagnosis of alpha- and beta-thalassemia.
Mensah C, Sheth S. Mensah C, et al. Hematology Am Soc Hematol Educ Program. 2021 Dec 10;2021(1):607-613. doi: 10.1182/hematology.2021000296. Hematology Am Soc Hematol Educ Program. 2021. PMID: 34889395 Free PMC article. Review.
In this article, we discuss the importance of carrier, prenatal, and newborn screening for thalassemia. We examine the rationale for who should be screened and when, as well as the current methodology for screening. ...Finally, a case-based overview of the approach for ind …
In this article, we discuss the importance of carrier, prenatal, and newborn screening for thalassemia. We examine the rationale for …
The Clinical Phenotypes of Alpha Thalassemia.
Lal A, Vichinsky E. Lal A, et al. Hematol Oncol Clin North Am. 2023 Apr;37(2):327-339. doi: 10.1016/j.hoc.2022.12.004. Hematol Oncol Clin North Am. 2023. PMID: 36907606 Review.
Clinical manifestations of alpha-thalassemia range from no symptoms to severe transfusion-dependent anemia. Alpha thalassemia trait is deletion of 1 to 2 alpha-globin genes, whereas alpha-thalassemia major (ATM; Barts hydrop …
Clinical manifestations of alpha-thalassemia range from no symptoms to severe transfusion-dependent anemia. Alpha th …
Alpha-thalassaemia.
Leung WC, Leung KY, Lau ET, Tang MH, Chan V. Leung WC, et al. Semin Fetal Neonatal Med. 2008 Aug;13(4):215-22. doi: 10.1016/j.siny.2008.02.006. Epub 2008 Apr 10. Semin Fetal Neonatal Med. 2008. PMID: 18406222 Review.
Alpha-thalassaemia is one of the most common human genetic disorders. Couples in which both partners carry alpha(0)-thalassaemia traits have a 25% risk of having a fetus affected by homozygous alpha-thalassaemia or haemoglobin Bart …
Alpha-thalassaemia is one of the most common human genetic disorders. Couples in which both partners carry alpha(0)- …
Thalassemia in Asia 2021 Overview of Thalassemia and Hemoglobinopathies in Bangladesh.
Chowdhury MA, Sultana R, Das D. Chowdhury MA, et al. Hemoglobin. 2022 Jan;46(1):7-9. doi: 10.1080/03630269.2021.2008957. Hemoglobin. 2022. PMID: 35950585 Review.
The health care system in Bangladesh is divided into primary secondary and tertiary levels, with each level having their own breakdown of available hospital beds and other treatment facilities. Thalassemia is a major health problem in Bangladesh. There are two types of …
The health care system in Bangladesh is divided into primary secondary and tertiary levels, with each level having their own breakdown of av …
Alpha-thalassaemia.
Bernini LF, Harteveld CL. Bernini LF, et al. Baillieres Clin Haematol. 1998 Mar;11(1):53-90. doi: 10.1016/s0950-3536(98)80070-x. Baillieres Clin Haematol. 1998. PMID: 10872473 Review.
alpha-Thalassaemias are genetic defects extremely frequent in some populations and are characterized by the decrease or complete suppression of alpha-globin polypeptide chains. ...Most probably the acquired alpha-thalassaemia is due to the lack …
alpha-Thalassaemias are genetic defects extremely frequent in some populations and are characterized by the decrease or comple …
Thalassemia in Asia 2021 Thalassemia in Brunei Darussalam.
Chong SC, Metassan S, Yusof N, Idros R, Johari N, Zulkipli IN, Ghani H, Lim MA, Taib S, Lu ZH, Abdul-Hamid MRW. Chong SC, et al. Hemoglobin. 2022 Jan;46(1):15-19. doi: 10.1080/03630269.2021.2008959. Hemoglobin. 2022. PMID: 35950589 Review.
In order to obtain reliable prevalence data, the gene frequencies of the thalassemias and other hemoglobinopathies should be investigated. Molecular studies on thalassemia have yet to be done for Brunei's population. ...Compiled data from 2009-2017 at the Hematology …
In order to obtain reliable prevalence data, the gene frequencies of the thalassemias and other hemoglobinopathies should be investig …
394 results