BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

79 related articles for article (PubMed ID: 24081202)

  • 1. Association of hemoglobin E-Saskatoon with hemoglobin S: report of the first case found in Brazil.
    Couto GK; Lorenzini PF; Pilger DA; Azevedo LA; Weber C; Macedo JL; Diedrich V; de Castro SM
    Acta Haematol; 2014; 131(2):84-7. PubMed ID: 24081202
    [No Abstract]   [Full Text] [Related]  

  • 2. The first case of a compound heterozygosity for Hb E-Saskatoon and HbS.
    Theodoridou S; Plata E; Karababa P; Loutradi A; Vyzantiadis T; Manitsa A
    Haematologica; 2003 Mar; 88(3):ECR08. PubMed ID: 12651286
    [No Abstract]   [Full Text] [Related]  

  • 3. β-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sβ⁰-thalassemia and their association with clinical and hematological features.
    Belisário AR; Martins ML; Brito AM; Rodrigues CV; Silva CM; Viana MB
    Acta Haematol; 2010; 124(3):162-70. PubMed ID: 20938172
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hemoglobin E-Saskatoon and pregnancy: report of two cases.
    Theodoridou S; Vyzantiadis TA; Theodoridis T; Tantanasis T; Karababa P; Loutradi A; Manitsa A
    J Obstet Gynaecol Res; 2006 Jun; 32(3):346-8. PubMed ID: 16764628
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and molecular characterization of hemoglobin Maputo [beta 47 (CD6) Asp > Tyr HBB: c.142G > T] and G-Ferrara [beta 57 (E1) Asn > Lys HBB: c.174C > A] in a newborn screening in Brazil.
    Silva MR; Sendin SM; Araujo IC; Pimentel FS; Viana MB
    Int J Lab Hematol; 2013 Dec; 35(6):e1-4. PubMed ID: 23279838
    [No Abstract]   [Full Text] [Related]  

  • 6. [Beta globin haplotypes in hemoglobin S carriers in Colombia].
    Durán CL; Morales OL; Echeverri SJ; Isaza M
    Biomedica; 2012; 32(1):103-11. PubMed ID: 23235792
    [TBL] [Abstract][Full Text] [Related]  

  • 7. HPLC-ESI-MS/MS analysis of hemoglobin peptides in tryptic digests of dried-blood spot extracts detects HbS, HbC, HbD, HbE, HbO-Arab, and HbG-Philadelphia mutations.
    Haynes CA; Guerra SL; Fontana JC; DeJesús VR
    Clin Chim Acta; 2013 Sep; 424():191-200. PubMed ID: 23796846
    [TBL] [Abstract][Full Text] [Related]  

  • 8. DNA diagnosis confirms hemoglobin deletion in newborn screen follow-up.
    Bhardwaj U; Zhang YH; Jackson DS; Buchanan GR; Therrell BL; McCabe LL; McCabe ER
    J Pediatr; 2003 Mar; 142(3):346-8. PubMed ID: 12640388
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC.
    Edison ES; Sathya M; Rajkumar SV; Nair SC; Srivastava A; Shaji RV
    Int J Lab Hematol; 2012 Oct; 34(5):556-8. PubMed ID: 22471768
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hb SE disease: a clinico-hematological profile.
    Mishra P; Pati HP; Chatterjee T; Dixit A; Choudhary DR; Srinivas MU; Mahapatra M; Choudhry VP
    Ann Hematol; 2005 Oct; 84(10):667-70. PubMed ID: 15947927
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hb S-São Paulo: a new sickling hemoglobin with stable polymers and decreased oxygen affinity.
    Jorge SE; Petruk AA; Kimura EM; Oliveira DM; Caire L; Suemasu CN; Silveira PA; Albuquerque DM; Costa FF; Skaf MS; Martínez L; Sonati Mde F
    Arch Biochem Biophys; 2012 Mar; 519(1):23-31. PubMed ID: 22244832
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hb Sheffield [β58(E2)Pro→His] in Oman: potential pitfall in genetic counseling.
    Al Zadjali S; Daar S; AlKindi S; Gravell D; Al Haddabi H; Berbar T; Krishnamoorthy R
    Hemoglobin; 2011; 35(2):111-6. PubMed ID: 21417567
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interaction of hemoglobin E with other abnormal hemoglobins.
    Edison ES; Shaji RV; Chandy M; Srivastava A
    Acta Haematol; 2011; 126(4):246-8. PubMed ID: 21986214
    [No Abstract]   [Full Text] [Related]  

  • 14. Hemoglobin SE disease in Maine, and severe thalassemia in New Hampshire.
    Thornburg CD; Steinberg MH; Chui DH
    J Pediatr Hematol Oncol; 2009 Apr; 31(4):307. PubMed ID: 19346889
    [No Abstract]   [Full Text] [Related]  

  • 15. Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.
    Daniel Y; Hill K; Inusa B; Thein SL; Howard J
    Hemoglobin; 2011; 35(4):406-10. PubMed ID: 21797706
    [TBL] [Abstract][Full Text] [Related]  

  • 16. First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders.
    Upadhye DS; Jain D; Nair SB; Nadkarni AH; Ghosh K; Colah RB
    J Clin Pathol; 2012 Jul; 65(7):654-9. PubMed ID: 22461654
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Incidence of Hb. S and Hb. E in twin cities of Hyderabad and Secunderabad.
    Reddi YR; Laxman S; Nagaraj Rao M
    Indian Pediatr; 1978 Jul; 15(7):535-6. PubMed ID: 721275
    [No Abstract]   [Full Text] [Related]  

  • 18. The first case of Hb E-Saskatoon [alpha 2 beta(2)22(B4)Glu-->Lys] in a Japanese male in Asia.
    Igarashi Y; Matsuzaki S; Kanou N; Inami S; Nakamura T; Kasai K; Fushitani K
    Hemoglobin; 1995; 19(6):403-6. PubMed ID: 8718699
    [No Abstract]   [Full Text] [Related]  

  • 19. Hemoglobin SE disease: a concise review.
    Masiello D; Heeney MM; Adewoye AH; Eung SH; Luo HY; Steinberg MH; Chui DH
    Am J Hematol; 2007 Jul; 82(7):643-9. PubMed ID: 17278112
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Hemoglobin anomalies and medico-biological data in 10,000 Africans (author's transl)].
    Coquelet ML; Jaeger G; Mullender N
    Nouv Rev Fr Hematol (1978); 1978 Nov; 20(3):465-77. PubMed ID: 754177
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.