BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 11924109)

  • 21. Thalassaemia and glucose-6-phosphate dehydrogenase deficiency in sickle-cell disorder patients in Taiz, Yemen.
    Al-Nood HA
    East Mediterr Health J; 2011 May; 17(5):404-8. PubMed ID: 21796953
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prevalence and Diversity of Haplotypes of Sickle Cell Disease in the Eastern Province of Saudi Arabia.
    Al-Ali AK; Alsulaiman A; Alzahrani AJ; Obeid OT; Vatte CB; Cyrus C; Alnafie AN; Alali RA; Alfarhan M; Mozeleski B; Steinberg MH
    Hemoglobin; 2020 Mar; 44(2):78-81. PubMed ID: 32448003
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The relationship of the genetic heterogeneity of sickle cell gene to clinical manifestations.
    el-Hazmi MA
    J Trop Pediatr; 1993 Feb; 39(1):23-9. PubMed ID: 8095305
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic Blood Disorders Survey in the Sultanate of Oman.
    Al-Riyami A; Ebrahim GJ
    J Trop Pediatr; 2003 Jul; 49 Suppl 1():i1-20. PubMed ID: 12934793
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Beta-globin gene cluster haplotypes in Yemeni children with sickle cell disease.
    Al-Saqladi AW; Brabin BJ; Bin-Gadeem HA; Kanhai WA; Phylipsen M; Harteveld CL
    Acta Haematol; 2010; 123(3):182-5. PubMed ID: 20224271
    [No Abstract]   [Full Text] [Related]  

  • 26. beta(S)-Globin gene cluster haplotypes in the West Bank of Palestine.
    Samarah F; Ayesh S; Athanasiou M; Christakis J; Vavatsi N
    Hemoglobin; 2009; 33(2):143-9. PubMed ID: 19373591
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prevalence of beta-thalassaemia and sickle cell traits in premarital screening in Al-Qassim, Saudi Arabia.
    El-Tayeb EN; Yaqoob M; Abdur-Rahim K; Gustavson KH
    Genet Couns; 2008; 19(2):211-8. PubMed ID: 18618996
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fibrocongestive splenomegaly in sickle cell disease: a distinct clinicopathological entity in the Eastern province of Saudi Arabia.
    Chopra R; Al-Mulhim AR; Al-Baharani AT
    Am J Hematol; 2005 Jul; 79(3):180-6. PubMed ID: 15981225
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prevalence of β-S Globin Haplotypes in Jazan Region of Saudi Arabia.
    Akhter MS; Mobarki AA; Hamali HA; Saboor M; Madkhali AM; Dobie G; Hobani YH; Eisa ZM
    Clin Lab; 2021 Aug; 67(8):. PubMed ID: 34383420
    [TBL] [Abstract][Full Text] [Related]  

  • 30. On the nature of sickle cell disease in the south-western province of Saudi Arabia.
    el-Hazmi MA; Warsy AS
    Acta Haematol; 1986; 76(4):212-6. PubMed ID: 2437751
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The effects of glucose-6-phosphate dehydrogenase deficiency on the haematological parameters and clinical manifestations in patients with sickle cell anaemia.
    el-Hazmi MA; Warsy AS
    Trop Geogr Med; 1989 Jan; 41(1):52-6. PubMed ID: 2763347
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cardiorenal risk prevalence in sickle cell hemoglobinopathy.
    Abo-Zenah H; Moharram M; El Nahas AM
    Nephron Clin Pract; 2009; 112(2):c98-c106. PubMed ID: 19390209
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Pulmonary function studies in Kuwaiti children with sickle cell disease and elevated Hb F.
    Hijazi Z; Onadeko BO; Khadadah M; Haider MZ; Adekile AD; Al-Habashi H
    Int J Clin Pract; 2005 Feb; 59(2):163-7. PubMed ID: 15854191
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The Xmn I site (-158, C----T) 5' to the G gamma gene: correlation with the Senegalese haplotype and G gamma globin expression.
    Ballas SK; Talacki CA; Adachi K; Schwartz E; Surrey S; Rappaport E
    Hemoglobin; 1991; 15(5):393-405. PubMed ID: 1724976
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Chromatographic analysis of Hb S for the diagnosis of various sickle cell disorders in Pakistan.
    Hashmi NK; Moiz B; Nusrat M; Hashmi MR
    Ann Hematol; 2008 Aug; 87(8):639-45. PubMed ID: 18465131
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Glucose-6-phosphate dehydrogenase variants and sickle cell genes in Al-Qunfuda, Saudi Arabia.
    el-Hazmi MA; Warsy AS
    Trop Geogr Med; 1991; 43(1-2):174-9. PubMed ID: 1750111
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Low bone mass due to sickle cell anemia: is it becoming a real issue?
    Sadat-Ali M; Al-Elq AH; Sultan O; Al-Turki H; Bukhari R; Al-Mulhim E
    West Afr J Med; 2008 Oct; 27(4):218-23. PubMed ID: 19469399
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Saudi Arabian type of homozygous sickle cell (SS) disease in the Netherlands: a case report.
    Aluoch JR
    Trop Geogr Med; 1986 Sep; 38(3):305-8. PubMed ID: 3750401
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sickle cell gene in the population of Saudi Arabia.
    el-Hazmi MA; Warsy AS; al-Swailem AR; al-Swailem AM; Bahakim HM
    Hemoglobin; 1996 Aug; 20(3):187-98. PubMed ID: 8854129
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.