BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 17805044)

  • 1. An Iranian child with HbQ-Iran [alpha75 (EF4) Asp-->His]/-alpha3.7 kb/IVSII.1 G-->A: first report.
    Rahimi Z; Akramipour R; Vaisi-Raygani A; Nagel RL; Muniz A
    J Pediatr Hematol Oncol; 2007 Sep; 29(9):649-51. PubMed ID: 17805044
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular and hematologic analysis of hemoglobin Q-Iran and hemoglobin Setif in Iranian families.
    Rahimi Z; Rezaei M; L Nagel R; Muniz A
    Arch Iran Med; 2008 Jul; 11(4):382-6. PubMed ID: 18588369
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hb D-Punjab [beta 121 (GH4) Glu-->Gln]/beta0-thalassemia [IVSII.1(G-->A)] in two cases from an Iranian family: first report.
    Rahimi Z; Akramipour R; Korani S; Nagel RL
    Am J Hematol; 2006 Apr; 81(4):302-3. PubMed ID: 16550524
    [No Abstract]   [Full Text] [Related]  

  • 4. A new alpha chain hemoglobin variant: Hb Al-Hammadi Riyadh [alpha75(EF4)Asp-->Val (alpha2)].
    Burnichon N; Lacan P; Becchi M; Zanella-Cleon I; Aubry M; Mowafy M; Couprie N; Francina A
    Hemoglobin; 2006; 30(2):155-64. PubMed ID: 16798639
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H
    Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hb North York [beta 117(G19)His-->Asp]: a new beta chain hemoglobin variant.
    Waye JS; Walker L; Nakamura LM; Eng B; McFarlane A
    Hemoglobin; 2009; 33(1):51-3. PubMed ID: 19205973
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. A severe alpha thalassemia case compound heterozygous for Hb Adana in alpha1 gene and 20.5 kb double gene deletion.
    Durmaz AA; Akin H; Ekmekci AY; Onay H; Durmaz B; Cogulu O; Aydinok Y; Ozkinay F
    J Pediatr Hematol Oncol; 2009 Aug; 31(8):592-4. PubMed ID: 19636270
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family.
    Akbari MT; Hamid M; Izadyar M
    Ann Hematol; 2011 Mar; 90(3):349-51. PubMed ID: 20521148
    [No Abstract]   [Full Text] [Related]  

  • 11. [The association of beta zero-thalassemia and Hb D Punjab in a family of Indian origin. The second case reported in Spain].
    Ropero P; González FA; Sánchez J; Armada B; Martí E; Valdés B; Mora A; Villegas A
    Med Clin (Barc); 1997 Mar; 108(10):385-8. PubMed ID: 9139146
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature.
    Kalotychou V; Tzanetea R; Konstantopoulos K; Papassotiriou I; Rombos I
    Hemoglobin; 2010; 34(4):383-8. PubMed ID: 20642336
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. alpha-thalassemia mutations in Khuzestan Province, Southwest Iran.
    Zandian K; Nateghi J; Keikhaie B; Pedram M; Hafezi-Nejad N; Hadavi V; Oberkanins C; Azarkeivan A; Law HY; Najmabadi H
    Hemoglobin; 2008; 32(6):546-52. PubMed ID: 19065332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.
    Luo HY; Heeney M; Wang WC; Eung SH; Ware RE; Steinberg MH; Chui DH
    Am J Hematol; 2006 May; 81(5):361-5. PubMed ID: 16628724
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients.
    Changtrakun Y; Fucharoen S; Ayukarn K; Siriratmanawong N; Fucharoen G; Sanchaisuriya K
    Ann Hematol; 2002 Jul; 81(7):389-93. PubMed ID: 12185510
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of mild and severely unstable alpha chain variants: the first observation of a compound heterozygote with Hb Setif [alpha94(G1)Asp-->Tyr (alpha2)] and Hb Agrinio [alpha29(B10)Leu-->Pro (alpha2)] in a Greek family.
    Douna V; Papassotiriou I; Stamoulakatou A; Metaxotou-Mavrommati A; Kanavakis E; Traeger-Synodinos J
    Hemoglobin; 2008; 32(6):592-5. PubMed ID: 19065338
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Preliminary identification of hemoglobin q-iran in an Iranian family from central province of Iran by globin chain analysis on HPLC.
    Khatami S; Najmabadi H; Rouhi S; Mirzazadeh R; Bayat P; Sadeghi S
    Arch Iran Med; 2013 Dec; 16(12):739-40. PubMed ID: 24329149
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequency of positive XmnIGgamma polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation.
    Neishabury M; Azarkeivan A; Najmabadi H
    Blood Cells Mol Dis; 2010; 44(2):95-9. PubMed ID: 19892574
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of alpha-thalassemia mutations in subjects from Eastern Sicily (Italy) with abnormal hematological indices and normal Hb A2.
    Di Bella C; Salpietro C; La Rosa M; Cuppari C; Piraino B; Cutri MR; Rigoli L
    Ann Hematol; 2006 Dec; 85(12):829-31. PubMed ID: 16951927
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.