These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 16533721)

  • 1. Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
    Harteveld CL; Steen G; Vlasveld LT; van Delft P; Giordano PC
    Haematologica; 2006 Apr; 91(4):570-1. PubMed ID: 16533721
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).
    Martin G; Villegas A; González FA; Ropero P; Hojas R; Polo M; Mateo M; Salvador M; Benavente C
    Hemoglobin; 2005; 29(2):113-7. PubMed ID: 15921163
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Hb Charlieu [alpha106(G13)Leu-->Pro (alpha1)]: a new phenotypically silent hemoglobin variant associated with a mild alpha-thalassemia phenotype.
    Joly P; Szymanowicz A; Neyron MJ; Zine A; Wajcman H; Francina A
    Hemoglobin; 2010; 34(4):366-73. PubMed ID: 20642334
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hb St. Truiden [α68(E17)Asn→His] and Hb Westeinde [α125(H8)Leu→Gln]: two new abnormalities of the α2-globin gene.
    Kaufmann JO; Phylipsen M; Neven C; Huisman W; van Delft P; Bakker-Verweij M; Arkesteijn SG; Harteveld CL; Giordano PC
    Hemoglobin; 2010; 34(5):439-44. PubMed ID: 20854117
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A rare thalassemic syndrome caused by interaction of Hb Adana [alpha59(E8)Gly-->Asp] with an alpha+-thalassemia deletion: clinical aspects in two cases.
    Douna V; Papassotiriou I; Garoufi A; Georgouli E; Ladis V; Stamoulakatou A; Metaxotou-Mavrommati A; Kanavakis E; Traeger-Synodinos J
    Hemoglobin; 2008; 32(4):361-9. PubMed ID: 18654886
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Alpha-thalassemia phenotype induced by the new IVS-II-2 (T --> A) splice donor site mutation on the alpha2-globin gene.
    Harteveld CL; Jebbink MC; van der Lely N; van Delft P; Akkermans N; Arkesteyn S; Giordano PC
    Hemoglobin; 2006; 30(1):3-7. PubMed ID: 16540408
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion.
    Harteveld CL; Versteegh FG; van Leer EH; Starreveld JS; Kok PJ; van Rooijen-Nijdam I; van Delft P; Zanella-Cleon I; Becchi M; Wajcman H; Giordano PC
    Hemoglobin; 2007; 31(3):313-23. PubMed ID: 17654068
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two new alpha-thalassemia point mutations that are undetectable by biochemical techniques.
    Joly P; Pégourie B; Courby S; Barro C; Besson G; Cohen L; Garcia C; Francina A
    Hemoglobin; 2008; 32(4):411-7. PubMed ID: 18654892
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha2 130 Ala --> Pro and Hb Caserta alpha2 26 Ala --> Thr) in a single HBA2 gene.
    Passarello C; Giambona A; Prossomariti L; Ammirabile M; Pucci P; Renda D; Pagano L; Maggio A
    Br J Haematol; 2008 Oct; 143(1):138-42. PubMed ID: 18691171
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hb Plasencia [α125(H8)Leu→Arg (α2)] is a frequent cause of α+-thalassemia in the Portuguese population.
    Cunha E; Bento C; Oliveira A; Relvas L; Neves J; Gameiro M; Barros C; Araújo A; Macedo A; Rocha P; Costa R; Maia T; Ribeiro ML
    Hemoglobin; 2013; 37(2):183-7. PubMed ID: 23368878
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia.
    Wajcman H; Traeger-Synodinos J; Papassotiriou I; Giordano PC; Harteveld CL; Baudin-Creuza V; Old J
    Hemoglobin; 2008; 32(4):327-49. PubMed ID: 18654884
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia.
    Srivorakun H; Fucharoen G; Puangplruk R; Kheawon N; Fucharoen S
    Eur J Haematol; 2011 Jul; 87(1):68-72. PubMed ID: 21447006
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interaction between (--SEA) alpha-thalassemia deletion and uncommon non-deletional alpha-globin gene mutations in Chinese patients.
    Ma ES; Chow EY; Chan AY; Chan LC
    Haematologica; 2001 May; 86(5):539-40. PubMed ID: 11410420
    [No Abstract]   [Full Text] [Related]  

  • 17. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand.
    Chunpanich S; Ayukarn K; Sanchaisuriya K; Fucharoen G; Fucharoen S
    Clin Lab Haematol; 2004 Oct; 26(5):355-8. PubMed ID: 15485467
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): two novel alpha2 gene mutations associated with mild alpha-thalassemia found in the same family after newborn screening.
    Giordano PC; Cnossen MH; Joosten AM; Jansen CA; Hakvoort TE; Bakker-Verweij M; Arkesteijn SG; van Delft P; Waye JS; Bouva MJ; Harteveld CL
    Hemoglobin; 2010; 34(4):354-65. PubMed ID: 20642333
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Further identification of the hyperunstable alpha-globin chain variant Hb Heraklion [codons 36/37 (-CCC); Pro-->0 (alpha1)] in Greek cases with co-inherited alpha+-thalassemia mutations.
    Douna V; Papassotiriou I; Metaxotou-Mavrommati A; Stamoulakatou A; Liapi D; Kampourakis D; Tsilimigaki A; Kanavakis E; Traeger-Synodinos J
    Hemoglobin; 2008; 32(4):379-85. PubMed ID: 18654888
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype.
    Lacerra G; Testa R; De Angioletti M; Schilirò G; Carestia C
    Hemoglobin; 2003 Aug; 27(3):149-59. PubMed ID: 12908799
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.