192 related articles for article (PubMed ID: 11045763)
21. Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations.
Singsanan S; Fucharoen G; Savongsy O; Sanchaisuriya K; Fucharoen S
Ann Hematol; 2007 Sep; 86(9):665-9. PubMed ID: 17589844
[TBL] [Abstract][Full Text] [Related]
22. Comparison of capillary electrophoregram among heterozygous Hb Hope, Hb Hope/α-thalassemia-1 SEA type deletion and Hb Hope/β(0)-thalassemia.
Pornprasert S; Panyasai S; Kongthai K
Clin Chem Lab Med; 2012 Mar; 50(9):1625-9. PubMed ID: 22962223
[TBL] [Abstract][Full Text] [Related]
23. Blood typing profile of a school-aged population of a North Togo township.
Vovor A; Fétéké L; Kueviakoe IM; Kpatarou L; Mawussi K; Magnang H; Ségbéna AY
Hemoglobin; 2014; 38(5):316-8. PubMed ID: 25271992
[TBL] [Abstract][Full Text] [Related]
24. Hemoglobin C--G-Georgia double heterozygosity: a case report.
Reynolds S; Miller C; King R; Lazarchick J
Ann Clin Lab Sci; 1992; 22(6):414-6. PubMed ID: 1456731
[TBL] [Abstract][Full Text] [Related]
25. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
Efremov GD
Hemoglobin; 2007; 31(1):1-15. PubMed ID: 17365000
[TBL] [Abstract][Full Text] [Related]
26. Hemoglobins in Togolese newborns: Hb S, Hb C, Hb Bart's, and alpha-globin gene status.
Segbena AY; Prehu C; Wajcman H; Bardakdjian-Michau J; Messie K; Feteke L; Vovor A; David M; Feingold J; Galacteros F
Am J Hematol; 1998 Nov; 59(3):208-13. PubMed ID: 9798658
[TBL] [Abstract][Full Text] [Related]
27. Heterozygous Hb Hope [beta136(H14)Gly --> Asp] in association with heterozygous beta0-thalassemia with apparent homozygous expression, in a Spanish patient.
Beneitez D; Carrera A; Duran-Suárez JR; Paz V; León A; García Talavera J
Hemoglobin; 2006; 30(1):45-9. PubMed ID: 16540415
[TBL] [Abstract][Full Text] [Related]
28. Inherited hemoglobin disorders in Guinea-Bissau, West Africa: a population study.
Masmas TN; Garly ML; Lisse IM; Rodriques A; Petersen PT; Birgens H
Hemoglobin; 2006; 30(3):355-64. PubMed ID: 16840226
[TBL] [Abstract][Full Text] [Related]
29. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC
Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
[TBL] [Abstract][Full Text] [Related]
30. Prenatal diagnosis of hemoglobin Bart's hydrops fetalis by HPLC analysis of hemoglobin in fetal blood samples.
Sanguansermsri T; Thanaratanakorn P; Steger HF; Tongsong T; Sirivatanapa P; Wanapirak C; Sirichotiyakul S; Chanprapas P; Flatz G
Southeast Asian J Trop Med Public Health; 2001 Mar; 32(1):180-5. PubMed ID: 11485083
[TBL] [Abstract][Full Text] [Related]
31. Molecular and hematological profiles of hemoglobin EE disease with different forms of alpha-thalassemia.
Fucharoen G; Trithipsombat J; Sirithawee S; Yamsri S; Changtrakul Y; Sanchaisuriya K; Fucharoen S
Ann Hematol; 2006 Jul; 85(7):450-4. PubMed ID: 16565831
[TBL] [Abstract][Full Text] [Related]
32. Description of the phenotypes of 63 heterozygous, homozygous and compound heterozygous patients carrying the Hb Groene Hart [α119(H2)Pro→Ser; HBA1: c.358C>T] variant.
Joly P; Lacan P; Garcia C; Francina A
Hemoglobin; 2014; 38(1):64-6. PubMed ID: 24111644
[TBL] [Abstract][Full Text] [Related]
33. [Abnormal hemoglobins and thalassemias in Mexico].
Ruiz-Reyes G
Rev Invest Clin; 1998; 50(2):163-70. PubMed ID: 9658939
[TBL] [Abstract][Full Text] [Related]
34. Hb Constant Spring [alpha 142, Term-->Gln (TAA>CAA in alpha2)] in the alpha-thalassemia of anemic patients in Myanmar.
Ne-Win ; Harano K; Harano T; Kyaw-Shwe ; Aye-Aye-Myint ; Khin-Thander-Aye ; Okada S
Hemoglobin; 2008; 32(5):454-61. PubMed ID: 18932070
[TBL] [Abstract][Full Text] [Related]
35. Abnormal hemoglobins found in Hunan.
Lu Y; Liu J
Chin Med J (Engl); 2003 Apr; 116(4):483-6. PubMed ID: 12875707
[TBL] [Abstract][Full Text] [Related]
36. [Homozygous hemoglobin constant spring in Guangxi province].
Chen P; Long GF; Lin WX; Li SQ
Zhonghua Xue Ye Xue Za Zhi; 2004 Apr; 25(4):205-8. PubMed ID: 15182556
[TBL] [Abstract][Full Text] [Related]
37. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
Viprakasit V; Tanphaichitr VS; Veerakul G; Chinchang W; Petrarat S; Pung-Amritt P; Higgs DR
Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
[TBL] [Abstract][Full Text] [Related]
38. Structural characterization of hemoglobin variants using capillary electrophoresis and fast atom bombardment mass spectrometry.
Ferranti P; Malorni A; Pucci P
Methods Enzymol; 1994; 231():45-65. PubMed ID: 7518889
[No Abstract] [Full Text] [Related]
39. Laboratory recognition of a rare hemoglobinopathy: hemoglobins SS and SG(Philadelphia) associated with alpha-thalassemia-2.
Kirk CM; Papadea CN; Lazarchick J
Arch Pathol Lab Med; 1999 Oct; 123(10):963-6. PubMed ID: 10506456
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
