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Longer titles found: Delta-beta thalassemia (view), Sickle cell-beta thalassemia (view)

searching for Beta thalassemia 40 found (137 total)

Mentzer index (315 words) [view diff] exact match in snippet view article find links to article

said to be helpful in differentiating iron deficiency anemia from beta thalassemia trait. Mentzer Index = MCV (fL) RBC (millions/ μ L ) {\displaystyle

Taraje Williams-Murray (148 words) [view diff] exact match in snippet view article find links to article

college. After an initial health scare where he was diagnosed with beta thalassemia, Taraje was able to continue to compete at a high level. He competed

Deferasirox (756 words) [view diff] no match in snippet view article find links to article

are receiving long-term blood transfusions for conditions such as beta-thalassemia and other chronic anemias. It is the first oral medication approved

Hemoglobin electrophoresis (540 words) [view diff] no match in snippet view article find links to article

levels are typically elevated in beta-thalassemia minor and hemoglobin F may be slightly increased. In beta-thalassemia major, hemoglobin A is decreased

Mina Izadyar (569 words) [view diff] no match in snippet view article find links to article

in planning and setting-up programs to curb the incidence of major beta-thalassemia as a major social health problem in Iran. These programs, which have

HBG1 (1,002 words) [view diff] no match in snippet view article find links to article

gamma globin expression is continued into adulthood. Also, in cases of beta-thalassemia and related conditions, gamma chain production may be maintained, possibly

JRI-Poland (414 words) [view diff] case mismatch in snippet view article find links to article

and Michael Tobias, and Steven Zedeck. Diamond was researching the Beta Thalassemia genetic trait, which he suspected was present in Ashkenazi Jewish families

ERAF (580 words) [view diff] no match in snippet view article find links to article

alpha-hemoglobin-stabilizing protein in normal erythropoiesis and beta-thalassemia". Ann. N. Y. Acad. Sci. 1054: 103–17. doi:10.1196/annals.1345.013.

Nucleated red blood cell (642 words) [view diff] exact match in snippet view article find links to article

blood cell count in pediatric patients with transfusion-dependent beta thalassemia". Menoufia Medical Journal. 33 (3): 949–955. Blood Smear: Details on

HBE1 (922 words) [view diff] no match in snippet view article find links to article

PMC 279587. PMID 3267215. Fei YJ, Stoming TA, Efremov GD, et al. (1988). "Beta-thalassemia due to a T----A mutation within the ATA box". Biochem. Biophys. Res

List of disorders included in newborn screening programs (716 words) [view diff] no match in snippet view article find links to article

African-Americans 1 in 400 Sickle-cell disease (Hb S/C) > 1 in 25,000 Hb S/Beta-Thalassemia (Hb S/Th) > 1 in 50,000 Inborn errors of amino acid metabolism Tyrosinemia

Hemoglobin O (1,419 words) [view diff] no match in snippet view article find links to article

R. L. (1985). "The interaction of hemoglobin O Arab with Hb S and beta+ thalassemia among Israeli Arabs". Human Genetics. 70 (2): 119–125. doi:10.1007/BF00273069

Deferiprone (889 words) [view diff] no match in snippet view article find links to article

long-term therapy with deferiprone in subjects with transfusion-dependent beta-thalassemia". Blood. 100 (5): 1566–9. doi:10.1182/blood-2002-01-0306. PMID 12176871

Acceleron Pharma (1,094 words) [view diff] no match in snippet view article find links to article

company's lead product luspatercept was in Phase III testing for MDS and beta-thalassemia. Acceleron experienced a drop in its share prices in 2019, after announcing

Hemoglobin, alpha 2 (1,381 words) [view diff] exact match in snippet view article find links to article

(Oct 2009). "Alpha globin gene numbers: an important modifier of HbE/beta thalassemia". Hematology. 14 (5): 297–300. doi:10.1179/102453309X446126. PMID 19843387

TATA box (4,806 words) [view diff] no match in snippet view article find links to article

Gonzalez-Redondo JM, Altay C, Gurgey A, Huisman TH (June 1988). "Beta-thalassemia due to a T----A mutation within the ATA box". Biochemical and Biophysical

Porphobilinogen deaminase (1,621 words) [view diff] no match in snippet view article find links to article

human beta-globin gene inhibits pre-mRNA splicing: a mechanism for beta+-thalassemia". Proc. Natl. Acad. Sci. U.S.A. 86 (3): 1041–5. Bibcode:1989PNAS.

CAP1 (857 words) [view diff] no match in snippet view article find links to article

interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians". Eur. J. Haematol

Antiochian Greek Christians (4,754 words) [view diff] case mismatch in snippet view article find links to article

Southeastern Turkey and Northern Israel. A study by Makhoul et al. (2010) on Beta Thalassemia Heterogeneity in Lebanon found out that the thalassemia mutations in

Nancy Olivieri (1,068 words) [view diff] no match in snippet view article find links to article

long-term therapy with deferiprone in subjects with transfusion-dependent beta-thalassemia". Blood. 100 (5): 1566–9. doi:10.1182/blood-2002-01-0306. PMID 12176871

Phaedon Fessas (1,879 words) [view diff] no match in snippet view article find links to article

27;1(7287):907-9. IF= 49 Peptide analysis of the inclusions of erythroid cells in beta-thalassemia. Fessas P, Loukopoulos D, Kaltsoya A. Biochim Biophys Acta. 1966 Aug

Hemoglobin D (3,699 words) [view diff] case mismatch in snippet view article find links to article

Kalyan Mansukhbhai (2017). "Co-Inheritance of Haemoglobin D-Punjab and Beta Thalassemia - A Rare Variant". Journal of Clinical and Diagnostic Research. 11

Celgene (2,800 words) [view diff] no match in snippet view article find links to article

products within several areas of research (MM, MDS, AML, Lymphoma, CLL, Beta-Thalassemia, Myelofibrosis, Solid Tumors, Inflammation & Immunology. In 2009, Dr

HBS1 like translational GTPase (844 words) [view diff] no match in snippet view article find links to article

in exon 1 of this gene is significantly associated with severity in beta-thalassemia/Hemoglobin E. Multiple alternatively spliced transcript variants encoding

Panteha Abareshi (746 words) [view diff] exact match in snippet view article find links to article

Abareshi was born with the genetic blood disorder, Sickle cell zero beta thalassemia which causes chronic pain and more pain as they age. Their blood disorder

Germline mutation (3,085 words) [view diff] no match in snippet view article find links to article

dominant point mutations within genes, including cystic fibrosis, beta-thalassemia, sickle-cell anemia, and Tay–Sachs disease. By inducing a double stranded

Hemoglobin subunit alpha (1,147 words) [view diff] no match in snippet view article find links to article

PMID 17512924. Ye BC, Zhang Z, Lei Z (2007). "Molecular analysis of alpha/beta-thalassemia in a southern Chinese population". Genet. Test. 11 (1): 75–83. doi:10

Evolutionary medicine (4,586 words) [view diff] no match in snippet view article find links to article

explain protection against falciparum malaria in sickle trait and beta-thalassemia trait". Blood. 104 (10): 3364–71. doi:10.1182/blood-2003-11-3820. PMID 15280204

Evolutionary medicine (4,586 words) [view diff] no match in snippet view article find links to article

explain protection against falciparum malaria in sickle trait and beta-thalassemia trait". Blood. 104 (10): 3364–71. doi:10.1182/blood-2003-11-3820. PMID 15280204

Genetic history of the Middle East (10,974 words) [view diff] case mismatch in snippet view article find links to article

which preceded the Crusades by more than four centuries." A study on Beta Thalassemia Heterogeneity in Lebanon found out that the thalassemia mutations in

Elivaldogene autotemcel (1,696 words) [view diff] exact match in snippet view article find links to article

decision came after the withdrawal of Zynteglo, a gene therapy for severe beta thalassemia, from Germany in 2021 due to similar difficulties in reaching reimbursement

Prevention of autosomal recessive disorders (600 words) [view diff] no match in snippet view article find links to article

Awofeso, AwoNiyi; Stanley, David (July 2016). "Carrier screening for beta-thalassemia in the Maldives: perceptions of parents of affected children who did

Red blood cell (7,853 words) [view diff] no match in snippet view article find links to article

including sepsis, haemolytic uremic syndrome, malaria, sickle cell anemia, beta-thalassemia, glucose-6-phosphate dehydrogenase deficiency, phosphate depletion

Duchenne muscular dystrophy (6,827 words) [view diff] no match in snippet view article find links to article

splice-targeted AONs to correct missplicing in cells removed from beta-thalassemia patients Wilton's group tested exon skipping for muscular dystrophy

Silent stroke (4,015 words) [view diff] no match in snippet view article find links to article

A; Arslan, S; Cesur, Y; Uner, A (2003). "Silent stroke in a case of beta-thalassemia major associated with chronic renal failure and diabetes mellitus"

Jeffrey Leiden (2,519 words) [view diff] exact match in snippet view article find links to article

potential for two human genetic diseases, sickle cell disease and beta thalassemia. Casgevy was approved for use in the UK (November 2023), the United

Genetic studies on Arabs (5,189 words) [view diff] no match in snippet view article find links to article

recessive followed by autosomal dominant. Some of the diseases are beta-thalassemia mutations, sickle-cell disease, congenital heart-disease, glucose-6-phosphate

William French Anderson (4,079 words) [view diff] no match in snippet view article find links to article

Nienhuis, A.W.; Anderson, W.F.: Cell-free hemoglobin synthesis in beta-thalassemia. Proc. Natl. Acad. Sci. USA, 67: 1854-1861, 1970. Nienhuis, A.W.; Laycock

Genetic studies on Moroccans (7,609 words) [view diff] no match in snippet view article find links to article

Abouyoub, A.; Levy, N.; Bennani, M. (December 2008). "Molecular basis of beta-thalassemia in Morocco: possible origins of the molecular heterogeneity". Genetic

List of OMIM disorder codes (18,877 words) [view diff] no match in snippet view article find links to article

187950; THPO Thrombocytopenia 4; 612004; CYCS Thrombocytopenia with beta-thalassemia, X-linked; 314050; GATA1 Thrombocytopenia, congenital amegakaryocytic;