157 related articles for article (PubMed ID: 7693620)
1. Hb Hradec Kralove (Hb HK) or alpha 2 beta 2 115(G17)Ala-->Asp, a severely unstable hemoglobin variant resulting in a dominant beta-thalassemia trait in a Czech family.
Divoky V; Svobodova M; Indrak K; Chrobak L; Molchanova TP; Huisman TH
Hemoglobin; 1993 Aug; 17(4):319-28. PubMed ID: 7693620
[TBL] [Abstract][Full Text] [Related]
2. [Dominant beta-thalassemia alleles in the Czech and Slovak population (beta-thalassemia mutations in 112(T-A) and 121(G-T) codons and the unstable Hradec Králové hemoglobin or alpha 2 beta 2 115 (G17) Ala-Asp)].
Indrák K; Divoký V; Brabec V; Chrobák L; Mociková K; Sakalová A; Svobodová M; Indráková J; Hammerová T; Zarnovicanová M
Vnitr Lek; 1994 Apr; 40(4):223-30. PubMed ID: 8184583
[TBL] [Abstract][Full Text] [Related]
3. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
Indrák K; Divoký V; Brabec V; Indráková J; Svobodová M; Huisman TH
Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
[TBL] [Abstract][Full Text] [Related]
4. Hb Lulu Island (alpha 2 beta 2 107[G9]Gly-->Asp)-beta zero- thalassemia (codon 15; TGG-->TAG), a form of thalassemia intermedia.
Gray GR; Manson HE; Gu LH; Leonova JYe ; Huisman TH
Am J Hematol; 1995 Sep; 50(1):26-9. PubMed ID: 7668221
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
7. Dominant beta-thalassemia with hemoglobin Hradec Kralove: enhanced hemolysis in the spleen.
Ohga S; Nomura A; Takada H; Kato J; Ideguchi H; Hattori Y; Suda M; Suita S; Hara T
Int J Hematol; 2003 Nov; 78(4):329-34. PubMed ID: 14686490
[TBL] [Abstract][Full Text] [Related]
8. Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.
Cürük MA; Dimovski AJ; Baysal E; Gu LH; Kutlar F; Molchanova TP; Webber BB; Altay C; Gürgey A; Huisman TH
Am J Hematol; 1993 Dec; 44(4):270-5. PubMed ID: 8237999
[TBL] [Abstract][Full Text] [Related]
9. A Korean family with a dominantly inherited beta-thalassemia due to Hb Durham-N.C./Brescia.
Kim JY; Park SS; Yang SH; Joo SI; Lee YJ; Ra EK; Shin S; Kim EC; Cho HI
Hemoglobin; 2001 Feb; 25(1):79-89. PubMed ID: 11300352
[TBL] [Abstract][Full Text] [Related]
10. [Analysis of clinical phenotype and genotype of unstable Hemoglobin Rush].
Ge S; Yang B; Yi W; Huang K; Liu H; Huang X; Chu J; Yang Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):15-20. PubMed ID: 28186586
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Hb Cardarelli [beta86(F2)Ala-->Pro]: a new unstable and hyperaffine variant in association with beta(+)-thalassemia.
Pagano L; Salzano AM; Carbone V; Iannelli D; Viola A; Pollio F; Prossomariti L; David O; Ricco G; Pucci P
Hemoglobin; 2004 May; 28(2):103-15. PubMed ID: 15182052
[TBL] [Abstract][Full Text] [Related]
13. Interactions of unstable hemoglobin Rush with thalassemia and hemoglobin E result in thalassemia intermedia.
Huang K; Ge S; Yi W; Bi H; Lin K; Sun H; Huang X; Chu J; Ma S; Yang Z
Hematology; 2019 Dec; 24(1):459-466. PubMed ID: 31124399
[No Abstract] [Full Text] [Related]
14. [Structural variants in hemoglobin occurring in the Czech Republic].
Indrák K; Brabec V; Divoký V; Fortová H; Suttnar J; Chrobák L; Wiedermann B; Huisman TH
Vnitr Lek; 1995 Jan; 41(1):13-20. PubMed ID: 7716887
[TBL] [Abstract][Full Text] [Related]
15. Hb Capa or alpha (2)94(G1)Asp-->Gly beta 2, a mildly unstable variant with an A-->G (GAC-->GGC) mutation in codon 94 of the alpha 1-globin gene.
Dinçol G; Dinçol K; Erdem S; Pobedimskaya DD; Molchanova TP; Ye Z; Webber BB; Wilson JB; Huisman TH
Hemoglobin; 1994 Jan; 18(1):57-60. PubMed ID: 8195009
[No Abstract] [Full Text] [Related]
16. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).
Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH
J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Hb Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemia.
Giordano PC; Harteveld CL; Streng H; Oosterwijk JC; Heister JG; Amons R; Bernini LF
Hemoglobin; 1994 Jan; 18(1):11-8. PubMed ID: 8195005
[TBL] [Abstract][Full Text] [Related]
19. Hb Florida: a novel elongated C-terminal beta-globin variant causing dominant beta-thalassemia phenotype.
Weinstein BI; Erramouspe B; Albuquerque DM; Oliveira DM; Kimura EM; Costa FF; Sonati MF
Am J Hematol; 2006 May; 81(5):358-60. PubMed ID: 16628732
[TBL] [Abstract][Full Text] [Related]
20. Association of Hb S/Hb lepore and delta beta-thalassemia/Hb lepore in Sicilian patients: review of the presence of Hb lepore in Sicily.
Mirabile E; Testa R; Consalvo C; Dickerhoff R; Schilirò G
Eur J Haematol; 1995 Aug; 55(2):126-30. PubMed ID: 7543057
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
