581 related articles for article (PubMed ID: 11042028)
1. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
[TBL] [Abstract][Full Text] [Related]
2. A novel beta-globin structural mutant, Hb Brescia (beta 114 Leu-Pro), causing a severe beta-thalassemia intermedia phenotype.
Murru S; Poddie D; Sciarratta GV; Agosti S; Baffico M; Melevendi C; Pirastu M; Cao A
Hum Mutat; 1992; 1(2):124-8. PubMed ID: 1301199
[TBL] [Abstract][Full Text] [Related]
3. Thalassemic hemoglobinopathies.
Steinberg MH; Adams JG
Am J Pathol; 1983 Dec; 113(3):396-409. PubMed ID: 6359893
[TBL] [Abstract][Full Text] [Related]
4. Low output hemoglobins which produce the phenotype of thalassemia.
Adams JG; Steinberg MH
Prog Clin Biol Res; 1981; 55():81-98. PubMed ID: 6895257
[TBL] [Abstract][Full Text] [Related]
5. The molecular basis of alpha-thalassemia in Thailand.
Winichagoon P; Fucharoen S; Wasi P
Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():7-13. PubMed ID: 1298997
[TBL] [Abstract][Full Text] [Related]
6. Modification of hemoglobin H disease by sickle trait.
Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF
J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
[TBL] [Abstract][Full Text] [Related]
7. Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodies.
Gasperini D; Galanello R; Melis MA; Iannelli S; Giordano P; Bernini LF; Cao A
Haematologica; 1992; 77(5):381-3. PubMed ID: 1336469
[TBL] [Abstract][Full Text] [Related]
8. Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy.
Podda A; Galanello R; Maccioni L; Melis MA; Rosatelli C; Perseu L; Cao A
Blood; 1991 Jan; 77(2):371-5. PubMed ID: 1985702
[TBL] [Abstract][Full Text] [Related]
9. Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
Bowden DK; Hill AV; Higgs DR; Oppenheimer SJ; Weatherall DJ; Clegg JB
J Clin Invest; 1987 Jan; 79(1):39-43. PubMed ID: 3793931
[TBL] [Abstract][Full Text] [Related]
10. alpha-globin gene deletions associated with Hb J Tongariki.
Bowden DK; Pressley L; Higgs DR; Clegg JB; Weatherall DJ
Br J Haematol; 1982 Jun; 51(2):243-9. PubMed ID: 6979350
[TBL] [Abstract][Full Text] [Related]
11. [Hemoglobinopathies in Japan].
Miyaji T
Rinsho Ketsueki; 1989 Aug; 30(8):1147-56. PubMed ID: 2601023
[TBL] [Abstract][Full Text] [Related]
12. Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.
Adams JG; Boxer LA; Baehner RL; Forget BG; Tsistrakis GA; Steinberg MH
J Clin Invest; 1979 May; 63(5):931-8. PubMed ID: 447835
[TBL] [Abstract][Full Text] [Related]
13. Beta-, delta beta-thalassemia and Hb lepore among Yugoslav, Bulgarian, Turkish and Albanian.
Efremov GD
Haematologica; 1990; 75 Suppl 5():31-41. PubMed ID: 2086380
[TBL] [Abstract][Full Text] [Related]
14. Thalassemias in Sardinia: molecular pathology, phenotype-genotype correlation, and prevention.
Cao A; Rosatelli C; Pirastu M; Galanello R
Am J Pediatr Hematol Oncol; 1991; 13(2):179-88. PubMed ID: 2069229
[TBL] [Abstract][Full Text] [Related]
15. Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.
Divoky V; Bissé E; Wilson JB; Gu LH; Wieland H; Heinrichs I; Prior JF; Huisman TH
Biochim Biophys Acta; 1992 Dec; 1180(2):173-9. PubMed ID: 1463768
[TBL] [Abstract][Full Text] [Related]
16. Rapid molecular characterization of mutations leading to unstable hemoglobin beta-chain variants.
Girodon E; Ghanem N; Vidaud M; Riou J; Martin J; Galactéros F; Goossens M
Ann Hematol; 1992 Oct; 65(4):188-92. PubMed ID: 1420507
[TBL] [Abstract][Full Text] [Related]
17. Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicine.
Akerman BR; Fujiwara TM; Lancaster GA; Morgan K; Scriver CR
Am J Med Genet; 1990 May; 36(1):76-84. PubMed ID: 2333910
[TBL] [Abstract][Full Text] [Related]
18. [Current views of thalassemia intermedia].
Longinotti M; Dore F; Oggiano L; Pardini S; Pistidda P; Guiso L; Frogheri L; Bonfigli S; Murineddu M; Rimini E
Recenti Prog Med; 1992 Apr; 83(4):233-40. PubMed ID: 1626119
[TBL] [Abstract][Full Text] [Related]
19. [Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family].
Dahmane-Arbane M; Blouquit Y; Arous N; Bardakdjian J; Benamani M; Riou J; Benabadji M; Rosa J; Galacteros F
Nouv Rev Fr Hematol (1978); 1987; 29(5):317-20. PubMed ID: 3438164
[TBL] [Abstract][Full Text] [Related]
20. [Analysis of a program for atypical familial microcytosis. Molecular basis of alpha-thalassemia].
Villegas Martínez A
Sangre (Barc); 1990 Aug; 35(4):277-88. PubMed ID: 2274839
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
