BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 18728358)

  • 1. Thromboembolic complications in splenectomized patients with dominantly inherited beta-thalassemia.
    Ohga S; Ideguchi H; Kato J; Ishimura M; Takada H; Harada N; Kawanaka H; Hattori Y; Kang D; Hamasaki N; Hara T
    Acta Haematol; 2008; 120(1):31-5. PubMed ID: 18728358
    [No Abstract]   [Full Text] [Related]  

  • 2. Hb Filottrano [codon 120 (-A)]: a novel frameshift mutation in exon 3 of the β-globin gene causing dominantly inherited β-thalassemia intermedia.
    Amato A; Cappabianca MP; Perri M; Zaghis I; Mastropietro F; Ponzini D; Di Biagio P; Piscitelli R
    Hemoglobin; 2012; 36(5):480-4. PubMed ID: 22992010
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Anticoagulant system activity in splenectomized versus non-splenectomized Iranian patients with beta-thalassemia major.
    Rashidi A; Alavi S; Arzanian MT; Ahmadinejad M
    Pediatr Hematol Oncol; 2007 Dec; 24(8):645-7. PubMed ID: 18092257
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Platelet aggregation and activation in thalassemia major patients in Indonesia.
    Setiabudy R; Wahidiyat PA; Setiawan L
    Clin Appl Thromb Hemost; 2008 Jul; 14(3):346-51. PubMed ID: 18160592
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A deletion of 11 bp (CD 131-134) in exon 3 of the beta-globin gene produces the phenotype of inclusion body beta-thalassemia.
    Ropero P; Villegas A; Martínez M; Ataulfo González Fernández F; Benavente C; Mateo M
    Ann Hematol; 2005 Sep; 84(9):584-7. PubMed ID: 15977037
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dominantly inherited beta thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the beta globin gene: Hb morgantown (beta91 CTG>CG).
    Luo HY; Tang W; Eung SH; Coad JE; Canfield P; Keller F; Crowell EH; Steinberg MH; Chui DH
    J Clin Pathol; 2005 Oct; 58(10):1110-2. PubMed ID: 16189162
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The spectrum of beta-thalassemia mutations in Azerbaijan.
    Tagiev AF; Surin VL; Gol'tsov AA; Lukianenko AV; Solovyev GYa ; Gulieva EA; Plutalov OV; Kaboev OK; Mamedova TA; Dadasheva TS
    Hum Mutat; 1993; 2(2):152-4. PubMed ID: 8318994
    [No Abstract]   [Full Text] [Related]  

  • 9. Hb Showa-Yakushiji [beta110(G12)Leu-->Pro] in four unrelated patients from west Bengal.
    Edison ES; Shaji RV; Devi SG; Kumar SS; Srivastava A; Chandy M
    Hemoglobin; 2005; 29(1):19-25. PubMed ID: 15768552
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family.
    Yi P; Yu F; Huang S; Zhong C; Li Q; Yang Y; Zhang W; Xiao C; Xu X
    Blood Cells Mol Dis; 2008; 41(1):56-9. PubMed ID: 18381244
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Platelet Aggregation Study in Patients With Hemoglobin Eβ Thalassemia in India.
    Ghosal T; Dolai TK; Mandal PK; Karthik S; Bandyopadhyay A
    Clin Appl Thromb Hemost; 2016 Sep; 22(6):575-80. PubMed ID: 25701765
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Increased platelet adhesion under flow conditions is induced by both thalassemic platelets and red blood cells.
    Goldschmidt N; Spectre G; Brill A; Zelig O; Goldfarb A; Rachmilewitz E; Varon D
    Thromb Haemost; 2008 Nov; 100(5):864-70. PubMed ID: 18989531
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hb L'Aquila [beta106(G8)Leu-->Val, CTG-->GTG]: a novel thalassemic hemoglobin variant.
    Amato A; Cappabianca MP; Ponzini D; Rinaldi S; Biagio PD; Foglietta E; Grisanti P; Mastropietro F
    Hemoglobin; 2007; 31(3):375-8. PubMed ID: 17654075
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Haemostatic disorders in nonsplenectomized and splenectomized thalassaemic children.
    Shebl SS; el-Sharkawy HM; el-Fadaly NH
    East Mediterr Health J; 1999 Nov; 5(6):1171-7. PubMed ID: 11924107
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The molecular analysis of beta-thalassemia mutations in Lorestan Province, Iran.
    Kiani AA; Mortazavi Y; Zeinali S; Shirkhani Y
    Hemoglobin; 2007; 31(3):343-9. PubMed ID: 17654071
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spontaneous platelet aggregation in thalassemic children and adolescents.
    Laosombat V; Wongchanchailert M; Kenpitak K; Wisitpongpon C
    Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():42-6. PubMed ID: 1298992
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pulmonary thromboembolism in thalassemic patients.
    Sonakul D; Fucharoen S
    Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():25-8. PubMed ID: 1298988
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Thromboembolic complications in beta-thalassemia: Beyond the horizon.
    Panigrahi I; Agarwal S
    Thromb Res; 2007; 120(6):783-9. PubMed ID: 17346783
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.