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456 related items for PubMed ID: 15854191

  • 1. 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
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  • 3. Pulmonary function abnormalities in children with sickle cell disease.
    Sylvester KP, Patey RA, Milligan P, Dick M, Rafferty GF, Rees D, Thein SL, Greenough A.
    Thorax; 2004 Jan; 59(1):67-70. PubMed ID: 14694252
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  • 4. Limitations of Hb F as a phenotypic modifier in sickle cell disease: study of Kuwaiti Arab patients.
    Adekile AD.
    Hemoglobin; 2011 Jan; 35(5-6):607-17. PubMed ID: 21999156
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  • 6. Correlates of Pulmonary Function in Children with Sickle Cell Disease and Elevated Fetal Hemoglobin.
    Adekile AD, Azab AF, Owayed A, Khadadah M.
    Med Princ Pract; 2018 Jan; 27(1):49-54. PubMed ID: 29183008
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  • 7. Pulmonary function correlates with body composition in Nigerian children and young adults with sickle cell disease.
    VanderJagt DJ, Trujillo MR, Jalo I, Bode-Thomas F, Glew RH, Agaba P.
    J Trop Pediatr; 2008 Apr; 54(2):87-93. PubMed ID: 17901067
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  • 9. 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 Apr; 16(4):286-90. PubMed ID: 17541294
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  • 11. Longitudinal changes in lung function and somatic growth in children with sickle cell disease.
    Koumbourlis AC, Lee DJ, Lee A.
    Pediatr Pulmonol; 2007 Jun; 42(6):483-8. PubMed ID: 17469146
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  • 12. Frequency of the 677 C-->T mutation of the methylenetetrahydrofolate reductase gene among Kuwaiti sickle cell disease patients.
    Adekile AD, Kutlar F, Haider MZ, Kutlar A.
    Am J Hematol; 2001 Apr; 66(4):263-6. PubMed ID: 11279637
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  • 17. Acute splenic sequestration in female children with sickle cell disease in the North of Jordan.
    Al-Rimawi HS, Abdul-Qader M, Jallad MF, Amarin ZO.
    J Trop Pediatr; 2006 Dec; 52(6):416-20. PubMed ID: 16951418
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  • 18. Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype.
    Italia K, Jain D, Gattani S, Jijina F, Nadkarni A, Sawant P, Nair S, Mohanty D, Ghosh K, Colah R.
    Blood Cells Mol Dis; 2009 Dec; 42(1):25-31. PubMed ID: 18954999
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  • 20. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
    Adekile A, Kutlar F, McKie K, Addington A, Elam D, Holley L, Clair B, Kutlar A.
    Eur J Haematol; 2005 Aug; 75(2):150-5. PubMed ID: 16004608
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