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 *

148 related articles for article (PubMed ID: 17952869)

  • 1. HPLC determination of hemoglobins to establish reference values with the aid of statistics and informatics.
    Ondei LS; Zamaro PJ; Mangonaro PH; Valêncio CR; Bonini-Domingos CR
    Genet Mol Res; 2007 Jun; 6(2):453-60. PubMed ID: 17952869
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromatographic measurements of hemoglobin A2 in blood samples that contain sickle hemoglobin.
    Shokrani M; Terrell F; Turner EA; Aguinaga MD
    Ann Clin Lab Sci; 2000 Apr; 30(2):191-4. PubMed ID: 10807164
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comparison of red blood cell hematology among normal, alpha-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy.
    Srisupundit K; Piyamongkol W; Tongsong T
    Am J Hematol; 2008 Dec; 83(12):908-10. PubMed ID: 18932192
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of Hb Constant Spring by a capillary electrophoresis method.
    Liao C; Zhou JY; Xie XM; Li J; Li R; Li DZ
    Hemoglobin; 2010 Jan; 34(2):175-8. PubMed ID: 20353355
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comparison between capillary electrophoresis and high performance liquid chromatography for detection and quantification of Hb constant spring [Hb CS; α142, Term→Gln (TAA>CAA IN α2)].
    Waneesorn J; Panyasai S; Kongthai K; Singboottra P; Pornprasert S
    Hemoglobin; 2011; 35(4):338-45. PubMed ID: 21797701
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Biochemical diagnosis in sickle cell disease.
    Isaacs WA
    Ghana Med J; 1971 Mar; 10(1):40-3. PubMed ID: 5173734
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hematological findings in 375 Sicilians with Hb S trait.
    Schilirò G; Comisi FF; Testa R; Dibenedetto SP; Samperi P; Marino S
    Haematologica; 1990; 75(2):113-6. PubMed ID: 2358201
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hemoglobin F concentration as a function of age in Kuwaiti sickle cell disease patients.
    Adekile A; Al-Kandari M; Haider M; Rajaa M; D'Souza M; Sukumaran J
    Med Princ Pract; 2007; 16(4):286-90. PubMed ID: 17541294
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hemoglobin A2 values in sickle cell disease patients quantified by high performance liquid chromatography and the influence of alpha thalassemia.
    da Fonseca SF; Amorim T; Purificação A; Gonçalves M; Boa-Sorte N
    Rev Bras Hematol Hemoter; 2015; 37(5):296-301. PubMed ID: 26408362
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comparison of methodologies for thalassemia screening by Hb A2 quantitation.
    Schmidt RM; Rucknagel DL; Necheles TF
    J Lab Clin Med; 1975 Nov; 86(5):873-82. PubMed ID: 1185043
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The detection and diagnosis of hemoglobin A2' by high-performance liquid chromatography.
    Van Kirk R; Sandhaus LM; Hoyer JD
    Am J Clin Pathol; 2005 May; 123(5):657-61. PubMed ID: 15981805
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular analysis of Iranian families with sickle cell disease.
    Ayatollahi M; Zakerinia M; Haghshenas M
    J Trop Pediatr; 2005 Jun; 51(3):136-40. PubMed ID: 15831669
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Abnormal hemoglobins identified in Martinique].
    Monplaisir N; Galacteros F; Arous N; Rhoda MD; Delanoe-Garin J; Ouka-Montjean M; de Linval JC; Rosa J
    Nouv Rev Fr Hematol (1978); 1985; 27(1):11-4. PubMed ID: 3991355
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haemoglobin electrophoresis patterns in Barbados.
    St John MA; Lungu FN
    West Indian Med J; 1999 Dec; 48(4):221-2. PubMed ID: 10639844
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H; Fucharoen G; Sae-Ung N; Sanchaisuriya K; Ratanasiri T; Fucharoen S
    Eur J Haematol; 2009 Jul; 83(1):57-65. PubMed ID: 19226360
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Plasma fibrinogen levels in Nigerian homozygous (Hb SS) sickle cell patients.
    Buseri FI; Shokunbi WA; Jeremiah ZA
    Hemoglobin; 2007; 31(1):89-92. PubMed ID: 17365009
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A comparison of three methods for quantitation of variant hemoglobin fractions.
    Pearce CJ
    Am J Med Technol; 1980 Oct; 46(10):698-703. PubMed ID: 7211934
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of thalassemia syndromes and abnormal hemoglobins in patients from the Aegean region of Turkey.
    Irken G; Oren H; Undar B; Duman M; Gülen H; Uçar C; Sanli N
    Turk J Pediatr; 2002; 44(1):21-4. PubMed ID: 11858374
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical phenotypes and molecular diagnosis in a hitherto interaction of Hb E/beta thalassemia syndrome (beta(E)/beta(-31), (A -->G)).
    Vathana N; Viprakasit V; Sanpakit K; Chinchang W; Veerakul G; Tanphaichitr V
    J Med Assoc Thai; 2005 Nov; 88 Suppl 8():S66-71. PubMed ID: 16856429
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neonatal screening for sickle cell disorders in Ouagadougou, Burkina Faso: a pilot study.
    Kafando E; Sawadogo M; Cotton F; Vertongen F; Gulbis B
    J Med Screen; 2005; 12(3):112-4. PubMed ID: 16156939
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.