355 related articles for article (PubMed ID: 24601859)
1. α-Thalassemia does not seem to influence erythrocyte deformability in sickle cell trait carriers.
Vayá A; Collado S; Alis R; Vera B; Romagnoli M; Barragán E
Hemoglobin; 2014; 38(3):165-8. PubMed ID: 24601859
[TBL] [Abstract][Full Text] [Related]
2. Rheological red blood cell behaviour in minor α-thalassaemia carriers.
Vayá A; Suescun M; Hernández JL; Pérez ML; Palanca S; Laiz B
Clin Hemorheol Microcirc; 2011; 48(4):241-6. PubMed ID: 22012829
[TBL] [Abstract][Full Text] [Related]
3. New insights provided by a comparison of impaired deformability with erythrocyte oxidative stress for sickle cell disease.
Barodka VM; Nagababu E; Mohanty JG; Nyhan D; Berkowitz DE; Rifkind JM; Strouse JJ
Blood Cells Mol Dis; 2014 Apr; 52(4):230-5. PubMed ID: 24246527
[TBL] [Abstract][Full Text] [Related]
4. The Hb E (HBB: c.79G>A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/- -
Leckngam P; Limweeraprajak E; Kiewkarnkha T; Tatu T
Hemoglobin; 2017 Jan; 41(1):38-43. PubMed ID: 28413893
[TBL] [Abstract][Full Text] [Related]
5. Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait.
Velasco-Rodríguez D; Alonso-Domínguez JM; González-Fernández FA; Muriel A; Abalo L; Sopeña M; Villarrubia J; Ropero P; Plaza MP; Tenorio M; Jiménez-Martín A; Moreno G; Martínez-Nieto J; de la Fuente-Gonzalo F; Fernández-Escribano M; López-Jiménez FJ; Cava F
J Clin Pathol; 2016 Oct; 69(10):912-20. PubMed ID: 26915371
[TBL] [Abstract][Full Text] [Related]
6. Erythrocyte deformability and aggregation in homozygous sickle cell disease.
Vayá A; Collado S; Dasí MA; Pérez ML; Hernandez JL; Barragán E
Clin Hemorheol Microcirc; 2014; 58(4):497-505. PubMed ID: 23603322
[TBL] [Abstract][Full Text] [Related]
7. Biophysical changes of red cells with thalassemia-like abnormal hemoglobin.
Bunyaratvej A; Fucharoen S; Tatsumi N
Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():86-90. PubMed ID: 1299000
[TBL] [Abstract][Full Text] [Related]
8. Rheological behaviour of red blood cells in beta and deltabeta thalassemia trait.
Vayá A; Iborra J; Falcó C; Moreno I; Bolufer P; Ferrando F; Pérez ML; Justo Aznar
Clin Hemorheol Microcirc; 2003; 28(2):71-8. PubMed ID: 12652012
[TBL] [Abstract][Full Text] [Related]
9. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
Muszlak M; Pissard S; Badens C; Chamouine A; Maillard O; Thuret I
Hemoglobin; 2015; 39(3):156-61. PubMed ID: 25806420
[TBL] [Abstract][Full Text] [Related]
10. α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.
Al-Riyami AZ; Daar S; Kindi SA; Madhani AA; Wali Y; Rawahi MA; Zadjali SA
Hemoglobin; 2020 Jan; 44(1):20-26. PubMed ID: 32019385
[TBL] [Abstract][Full Text] [Related]
11. Sickle cell anemia and α-thalassemia: a modulating factor in homozygous HbS/S patients in Oman.
Hassan SM; Al Muslahi M; Al Riyami M; Bakker E; Harteveld CL; Giordano PC
Eur J Med Genet; 2014; 57(11-12):603-6. PubMed ID: 25266642
[TBL] [Abstract][Full Text] [Related]
12. Hematological findings in 375 Sicilians with Hb S trait.
Schilirò G; Comisi FF; Testa R; Dibenedetto SP; Samperi P; Marino S
Haematologica; 1990; 75(2):113-6. PubMed ID: 2358201
[TBL] [Abstract][Full Text] [Related]
13. Association of erythrocyte deformability with red blood cell distribution width in metabolic diseases and thalassemia trait.
Vayá A; Alis R; Suescún M; Rivera L; Murado J; Romagnoli M; Solá E; Hernandez-Mijares A
Clin Hemorheol Microcirc; 2015; 61(3):407-15. PubMed ID: 25062717
[TBL] [Abstract][Full Text] [Related]
14. Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties.
Lamarre Y; Romana M; Lemonne N; Hardy-Dessources MD; Tarer V; Mougenel D; Waltz X; Tressières B; Lalanne-Mistrih ML; Etienne-Julan M; Connes P
Clin Hemorheol Microcirc; 2014; 57(1):63-72. PubMed ID: 24004554
[TBL] [Abstract][Full Text] [Related]
15. KFL1 Gene Variants in α-Thalassemia Individuals with Increased Fetal Hemoglobin in a Chinese Population.
Jiang F; Qu YX; Chen GL; Li J; Zhou JY; Zuo LD; Liao C; Li DZ
Hemoglobin; 2018 May; 42(3):161-165. PubMed ID: 30205725
[TBL] [Abstract][Full Text] [Related]
16. Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-thalassemia codon 17 (A>T) in a Thai patient.
Pornprasert S; Panyasai S; Kongthai K; Treesuwan K
Hemoglobin; 2012; 36(3):265-9. PubMed ID: 22471390
[TBL] [Abstract][Full Text] [Related]
17. Sickle cell rheology is determined by polymer fraction--not cell morphology.
Hiruma H; Noguchi CT; Uyesaka N; Hasegawa S; Blanchette-Mackie EJ; Schechter AN; Rodgers GP
Am J Hematol; 1995 Jan; 48(1):19-28. PubMed ID: 7832188
[TBL] [Abstract][Full Text] [Related]
18. Does higher red blood cell (RBC) lactate transporter activity explain impaired RBC deformability in sickle cell trait?
Connes P; Sara F; Hardy-Dessources MD; Etienne-Julan M; Hue O
Jpn J Physiol; 2005 Dec; 55(6):385-7. PubMed ID: 16441976
[TBL] [Abstract][Full Text] [Related]
19. [Analysis of hematological characteristics on the 79 co-inheritance of α-thalassemia and β-thalassemia carriers in Guangxi].
Xiong F; Lou JW; Wei XF; Sun MN; Huang JW; Shang X; Zhang XH; Xu XM
Zhonghua Xue Ye Xue Za Zhi; 2012 Oct; 33(10):856-60. PubMed ID: 23384911
[TBL] [Abstract][Full Text] [Related]
20. α0-Thalassemia trait with normal red cell indices: a report of two cases.
Liao C; Li DZ
Hemoglobin; 2012; 36(6):589-91. PubMed ID: 23181749
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
