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 *

103 related articles for article (PubMed ID: 23795655)

  • 21. Hb Phimai [β72(E16)Ser→Thr]: a novel β-globin structural variant found in association with Hb constant spring in pregnancy.
    Singsanan S; Srivorakun H; Fucharoen G; Puangplruk R; Fucharoen S
    Hemoglobin; 2011; 35(2):103-10. PubMed ID: 21417566
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two different mutations in codon 97 of the beta-globin gene cause Hb Malmö in Sweden.
    Landin B; Berglund S; Wallman K
    Am J Hematol; 1996 Jan; 51(1):32-6. PubMed ID: 8571935
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Homozygosity for hemoglobin O-Arab (alpha 2 beta 2 121 Glu----Lys). Hb O-Arab disease.
    Altay C; Gürgey A; Huisman TH
    Turk J Pediatr; 1986; 28(1):67-72. PubMed ID: 3727027
    [No Abstract]   [Full Text] [Related]  

  • 25. Rare hemoglobin variants in Tunisian population.
    Zorai A; Moumni I; Mosbahi I; Douzi K; Chaouachi D; Guemira F; Abbes S
    Int J Lab Hematol; 2015 Apr; 37(2):148-54. PubMed ID: 24905386
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Case series of HbQ-India, a rare alpha globin variant in a referral laboratory setting in South India.
    Shaik A; Thekkelakayil ST; Kumawat V; Gupta A; Goyal M
    Indian J Pathol Microbiol; 2020; 63(3):481-484. PubMed ID: 32769347
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A comprehensive analysis of hemoglobin variants by high-performance liquid chromatography (HPLC).
    Szuberski J; Oliveira JL; Hoyer JD
    Int J Lab Hematol; 2012 Dec; 34(6):594-604. PubMed ID: 22713122
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Rare form of autosomal dominant thalassemia--hemoglobin Hakkari.
    Nair S; Eldjerou LK; Harris NS; Dunbar LN
    Pediatr Blood Cancer; 2014 Nov; 61(11):2118-20. PubMed ID: 24789613
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Regulation of the β-globin gene family expression, useful in the search for new therapeutic targets for hemoglobinopathies].
    Scheps KG; Varela V
    Medicina (B Aires); 2016; 76(6):383-389. PubMed ID: 27959850
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Hemoglobinopathies in Caribbean Basin countries].
    Sáenz Renauld GF
    Rev Biol Trop; 1988 Nov; 36(2B):361-72. PubMed ID: 3078798
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Spectrum of hemoglobinopathies in the state of Orissa, India: a ten years cohort study.
    Balgir RS
    J Assoc Physicians India; 2005 Dec; 53():1021-6. PubMed ID: 16572956
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hemoglobin variants in Cyprus.
    Kyrri AR; Felekis X; Kalogerou E; Wild BJ; Kythreotis L; Phylactides M; Kleanthous M
    Hemoglobin; 2009; 33(2):81-94. PubMed ID: 19373583
    [TBL] [Abstract][Full Text] [Related]  

  • 33. HbQ-India (HBA1:c.193G>C): hematological profiles and unique CE-HPLC findings of potential diagnostic utility in 65 cases.
    Sharma S; Sharma P; Das R; Chhabra S; Hira JK
    Ann Hematol; 2017 Jul; 96(7):1227-1229. PubMed ID: 28526955
    [No Abstract]   [Full Text] [Related]  

  • 34. Hemoglobinopathies in childhood (a study of 51 cases).
    Giri DD; Patra SB; Patel RZ
    Indian J Pathol Microbiol; 1984 Apr; 27(2):81-9. PubMed ID: 6511037
    [No Abstract]   [Full Text] [Related]  

  • 35. Prevalence of hemoglobinopathies in rural Bengal, India.
    Dolai TK; Dutta S; Bhattacharyya M; Ghosh MK
    Hemoglobin; 2012; 36(1):57-63. PubMed ID: 22004064
    [TBL] [Abstract][Full Text] [Related]  

  • 36. High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa).
    Millimono TS; Loua KM; Rath SL; Relvas L; Bento C; Diakite M; Jarvis M; Daries N; Ribeiro LM; Manco L; Kaeda JS
    Hemoglobin; 2012; 36(1):25-37. PubMed ID: 21929367
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Extended molecular spectrum of beta- and alpha-thalassemia in Oman.
    Hassan SM; Hamza N; Jaffer Al-Lawatiya F; Jaffer Mohammed A; Harteveld CL; Rajab A; Giordano PC
    Hemoglobin; 2010 Jan; 34(2):127-34. PubMed ID: 20353347
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Case report: prenatal diagnosis of Hb Hammersmith [β42(CD1)Phe→Ser; HBB: c.128T > C] in a family with an adult male patient.
    Li R; Wang T; Xie XM; Li DZ
    Hemoglobin; 2014; 38(2):142-5. PubMed ID: 24471820
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hemoglobinopathies in a hospital population in Vancouver.
    Gray GR; Marion RB
    Can Med Assoc J; 1978 Oct; 119(7):701-4. PubMed ID: 709469
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Polymerase chain reaction-based search for two alpha-globin gene mutations in India.
    Bhattacharya G; Sarkar AA; Banerjee D; Chandra S; Das M; Dasgupta UB
    Hemoglobin; 2008; 32(5):485-90. PubMed ID: 18932074
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.