BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

302 related articles for article (PubMed ID: 749927)

  • 1. Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia.
    Pembrey ME; Wood WG; Weatherall DJ; Perrine RP
    Br J Haematol; 1978 Nov; 40(3):415-29. PubMed ID: 749927
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fetal haemoglobin level--effect of gender, age and haemoglobin disorders.
    el-Hazmi MA; Warsy AS; Addar MH; Babae Z
    Mol Cell Biochem; 1994 Jun; 135(2):181-6. PubMed ID: 7530809
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hb F synthesis in sickle cell anaemia: a comparison of Saudi Arab cases with those of African origin.
    Wood WG; Pembrey ME; Serjeant GR; Perrine RP; Weatherall DJ
    Br J Haematol; 1980 Jul; 45(3):431-45. PubMed ID: 6158984
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin.
    Haghshenass M; Ismail-Beigi F; Clegg JB; Weatherall DJ
    J Med Genet; 1977 Jun; 14(3):168-71. PubMed ID: 881705
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High fetal hemoglobin production in sickle cell anemia in the eastern province of Saudi Arabia is genetically determined.
    Miller BA; Salameh M; Ahmed M; Wainscoat J; Antognetti G; Orkin S; Weatherall D; Nathan DG
    Blood; 1986 May; 67(5):1404-10. PubMed ID: 2421808
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effect of alpha thalassaemia, G-6-PD deficiency and Hb F on the nature of sickle cell anaemia in south-western Saudi Arabia.
    el-Hazmi MA; al-Swailem AR; Bahakim HM; al-Faleh FZ; Warsy AS
    Trop Geogr Med; 1990 Jul; 42(3):241-7. PubMed ID: 1705730
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Non-benign sickle cell anaemia in western Saudi Arabia.
    Acquaye JK; Omer A; Ganeshaguru K; Sejeny SA; Hoffbrand AV
    Br J Haematol; 1985 May; 60(1):99-108. PubMed ID: 2408655
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
    Adeyemo T; Ojewunmi O; Oyetunji A
    Pan Afr Med J; 2014; 18():71. PubMed ID: 25400838
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Post-natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parenteral Hb F levels.
    Mason KP; Grandison Y; Hayes RJ; Serjeant BE; Serjeant GR; Vaidya S; Wood WG
    Br J Haematol; 1982 Nov; 52(3):455-63. PubMed ID: 6181802
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Foetal haemoglobin levels in sickle cell anaemia in Nigerians.
    Falusi AG; Esan GJ
    Afr J Med Med Sci; 1989 Jun; 18(2):145-9. PubMed ID: 2474239
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes.
    Murray N; Serjeant BE; Serjeant GR
    Br J Haematol; 1988 May; 69(1):89-92. PubMed ID: 2454649
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sickle beta 0 thalassemia in Eastern Saudi Arabia.
    Pembrey ME; Perrine RP; Wood WG; Weatherall DJ
    Am J Hum Genet; 1980 Jan; 32(1):26-41. PubMed ID: 6153864
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sickle cell-beta 0-thalassaemia in Saudi Arabia.
    el-Hazmi MA; Al-Swailem AR
    Hum Hered; 1987; 37(4):211-6. PubMed ID: 2443440
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequency of foetal haemoglobin and haemoglobin values in various haemoglobin genotypes in Calabar, Nigeria.
    Uko EK; Useh MF; Gwanmesia FN
    East Afr Med J; 1997 Dec; 74(12):809-11. PubMed ID: 9557428
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sickle cell disease in Saudi Arabs in early childhood.
    Perrine RP; John P; Pembrey M; Perrine S
    Arch Dis Child; 1981 Mar; 56(3):187-92. PubMed ID: 6163399
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Heterogeneity and variation of clinical and haematological expression of haemoglobin S in Saudi Arabs.
    el-Hazmi MA
    Acta Haematol; 1992; 88(2-3):67-71. PubMed ID: 1281601
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Relationship of haemoglobin F and alpha thalassaemia to severity of sickle-cell anaemia in the Eastern Province of Saudi Arabia.
    Al-Awamy BH; Niazi GA; el-Mouzan MI; Altorki MT; Naeem MA
    Ann Trop Paediatr; 1986 Dec; 6(4):261-5. PubMed ID: 2435232
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Homozygous sickle cell disease and priapism in the eastern province of Saudi Arabia.
    Taha SA; Sharayah A; Salem A; Knox-Macaulay H
    Acta Haematol; 1987; 77(1):60-1. PubMed ID: 2437752
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical manifestation and laboratory findings of sickle cell anaemia in association with alpha-thalassaemia in Saudi Arabia.
    el-Hazmi MA
    Acta Haematol; 1985; 74(3):155-60. PubMed ID: 2420134
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.