139 related articles for article (PubMed ID: 1705322)
1. Hematologic data in 825 cases of beta-thalassemia trait in Spain.
Calero F; Villegas A; Porres A; Valverde F; del Potro E; Sánchez P; Luque JM; Espinós D
Nouv Rev Fr Hematol (1978); 1990; 32(4):265-70. PubMed ID: 1705322
[TBL] [Abstract][Full Text] [Related]
2. Haematological and clinical data in 200 cases of thalassaemia trait in eastern Spain.
Vayá A; Carratalá A; Martinez C; Aznar J
Nouv Rev Fr Hematol (1978); 1983; 25(6):369-73. PubMed ID: 6198618
[TBL] [Abstract][Full Text] [Related]
3. The contribution of red cell morphology to the diagnosis of beta-thalassemia trait.
Joishy SK; Shafer JA; Rowley PT
Blood Cells; 1986; 11(3):367-74. PubMed ID: 3742056
[TBL] [Abstract][Full Text] [Related]
4. Developmental changes in hemoglobin F levels during the first two years of life in normal and heterozygous beta-thalassemia infants.
Metaxotou-Mavromati AD; Antonopoulou HK; Laskari SS; Tsiarta HK; Ladis VA; Kattamis CA
Pediatrics; 1982 Jun; 69(6):734-8. PubMed ID: 6176937
[TBL] [Abstract][Full Text] [Related]
5. Cord blood study on beta-thalassemia and hemoglobin E.
Pootrakul S; Muang-sup V; Fucharoen S; Wasi P
Am J Med Genet; 1988 Jan; 29(1):49-57. PubMed ID: 2449818
[TBL] [Abstract][Full Text] [Related]
6. Thalassemia in the outpatient department of the Yangon Children's Hospital in Myanmar: basic hematological values of thalassemia traits.
Khin Ei Han ; Aung Myo Han ; Kyaw Win ; Thein Thein Myint
Southeast Asian J Trop Med Public Health; 1992 Jun; 23(2):264-8. PubMed ID: 1439979
[TBL] [Abstract][Full Text] [Related]
7. Genetic heterogeneity of beta zero-thalassemia intermedia in Southern Sardinia.
Cacace E; Frigerio R; Olla N; Sole G; Mela Q; Perpignano G; Carcassi U
Haematologica; 1985; 70(2):95-100. PubMed ID: 2408975
[No Abstract] [Full Text] [Related]
8. Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene.
Traeger-Synodinos J; Papassotiriou I; Vrettou C; Skarmoutsou C; Stamoulakatou A; Kanavakis E
Haematologica; 2001 Apr; 86(4):363-7. PubMed ID: 11325640
[TBL] [Abstract][Full Text] [Related]
9. [Hematological data analysis in children with thalassemia trait or hemoglobin H disease in Taiwan].
Yang CP; Hung IJ
J Formos Med Assoc; 1991 Jun; 90(6):591-7, 586. PubMed ID: 1681007
[TBL] [Abstract][Full Text] [Related]
10. Diagnostic significance of hemoglobin F and A2 levels in homo- and heterozygous beta-thalassemia during infancy.
Schröter W; Nafz C
Helv Paediatr Acta; 1981; 36(6):519-25. PubMed ID: 6174481
[TBL] [Abstract][Full Text] [Related]
11. [Hematometric values in delta-beta thalassemia minor. Special importance of the erythrocyte distribution in comparison with beta thalassemia and iron deficiency].
Juncá Piera J; Farré Guerrero V; Gaspar CR; Flores López A; Roncalés Mateo FJ; Millá Santos F
Sangre (Barc); 1990 Apr; 35(2):134-6. PubMed ID: 2152545
[TBL] [Abstract][Full Text] [Related]
12. Age and sex matched analysis of Hb Lepore trait in a new population in Spain.
Gilsanz F; Vela JG; Núñez GM
Nouv Rev Fr Hematol (1978); 1992; 34(2):163-6. PubMed ID: 1502023
[TBL] [Abstract][Full Text] [Related]
13. [Heterozygous beta-thalassemia without icrease of hemoglobin A2].
Marti HR; Grieder HR
Schweiz Med Wochenschr; 1970 Apr; 100(15):663-6. PubMed ID: 5438669
[No Abstract] [Full Text] [Related]
14. Frequency of delta+ 27-thalassaemia in Sardinians.
Guiso L; Frogheri L; Pistidda P; Angioni L; Dore F; Pardini S; Longinotti M
Clin Lab Haematol; 1996 Dec; 18(4):241-4. PubMed ID: 9054695
[TBL] [Abstract][Full Text] [Related]
15. Flow cytometric measurement of hemoglobin F in RBCs: diagnostic usefulness in the distinction of hereditary persistence of fetal hemoglobin (HPFH) and hemoglobin S-hPFH from other conditions with elevated levels of hemoglobin F.
Hoyer JD; Penz CS; Fairbanks VF; Hanson CA; Katzmann JA
Am J Clin Pathol; 2002 Jun; 117(6):857-63. PubMed ID: 12047136
[TBL] [Abstract][Full Text] [Related]
16. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
Panyasai S; Fucharoen S; Surapot S; Fucharoen G; Sanchaisuriya K
Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
[TBL] [Abstract][Full Text] [Related]
17. [Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child].
Haji F; Chadli A; Fattoum S; Souilem J; Hassine L
Arch Inst Pasteur Tunis; 1985 Dec; 62(4):341-53. PubMed ID: 2423045
[TBL] [Abstract][Full Text] [Related]
18. Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levels.
Galanello R; Melis MA; Furbetta M; Angius A; Scalas MT; Paglietti E; Cao A
Nouv Rev Fr Hematol (1978); 1981; 23(4):193-5. PubMed ID: 7312613
[TBL] [Abstract][Full Text] [Related]
19. [Evaluation of erythrocyte deformability in carriers of thalassemic trait with the Hanss' hemorheometer].
Vayá A; Mira Y; Martínez M; Miralles F; Aguado C; Aznar J
Sangre (Barc); 1989 Feb; 34(1):50-2. PubMed ID: 2711286
[TBL] [Abstract][Full Text] [Related]
20. Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.
Galanello R; Podda A; Melis MA; Monne M; Cao A
Prog Clin Biol Res; 1989; 316B():113-21. PubMed ID: 2482492
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
