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 *

211 related articles for article (PubMed ID: 11924109)

  • 61. Sickle cell anemia in Garasia tribals of Rajasthan.
    Mandot S; Khurana VL; Sonesh JK
    Indian Pediatr; 2009 Mar; 46(3):239-40. PubMed ID: 19179738
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Silent brain infarcts are rare in Kuwaiti children with sickle cell disease and high Hb F.
    Adekile AD; Yacoub F; Gupta R; Sinan T; Haider MZ; Habeeb Y; Al-Bloushi M; Moosa A
    Am J Hematol; 2002 Jul; 70(3):228-31. PubMed ID: 12111768
    [TBL] [Abstract][Full Text] [Related]  

  • 63. A case of homozygous sickle cell disease in Sri Lanka.
    Lucas GN; Jayawardena DR
    Ceylon Med J; 1991 Dec; 36(4):172-4. PubMed ID: 1725506
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [Infections in Senegalese children and adolescents with sickle cell anemia: epidemiological aspects].
    Diagne I; Soares GM; Gueye A; Diagne-Gueye NR; Fall L; N'Diaye O; Camara B; Diouf S; Fall M
    Dakar Med; 2000; 45(1):55-8. PubMed ID: 14666792
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Analysis of high fetal hemoglobin production in sickle cell anemia patients from the Eastern Province of Saudi Arabia.
    Miller BA; Salameh M; Ahmed M; Olivieri N; Huisman TH; Orkin SH; Nathan DG
    Prog Clin Biol Res; 1987; 251():415-26. PubMed ID: 2448810
    [No Abstract]   [Full Text] [Related]  

  • 66. Spectrum of hereditary coagulation factor deficiencies in eastern province, Saudi Arabia.
    Islam SI; Quadri MI
    East Mediterr Health J; 1999 Nov; 5(6):1188-95. PubMed ID: 11924110
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Glucose-6-phosphate dehydrogenase deficiency and sickle cell genes in Bisha.
    el-Hazmi MA; al-Swailem A; Warsy AS
    J Trop Pediatr; 1995 Aug; 41(4):225-9. PubMed ID: 7563275
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease.
    Ofori-Acquah SF; Lalloz MR; Serjeant G; Layton DM
    Cell Mol Biol (Noisy-le-grand); 2004 Feb; 50(1):35-42. PubMed ID: 15040425
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Hydroxyurea in sickle cell disease patients from Eastern Saudi Arabia.
    Al-Jam'a AH; Al-Dabbous IA
    Saudi Med J; 2002 Mar; 23(3):277-81. PubMed ID: 11938415
    [TBL] [Abstract][Full Text] [Related]  

  • 70. The consequences and implications of the multicentric origin of the Hb S gene.
    Nagel RL; Labie D
    Prog Clin Biol Res; 1985; 191():93-103. PubMed ID: 2413486
    [No Abstract]   [Full Text] [Related]  

  • 71. Hematological observations on Arabian SS patients with a homozygosity or heterozygosity for a beta S chromosome with haplotype #31.
    Kutlar A; Hattori Y; Bakioglu I; Kutlar F; Kamel K; Huisman TH
    Hemoglobin; 1985; 9(6):545-57. PubMed ID: 2419279
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Survey of sickle cell disease in Italy.
    Russo-Mancuso G; Romeo MA; Guardabasso V; Schilirò G
    Haematologica; 1998 Oct; 83(10):875-81. PubMed ID: 9830795
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Polymorphisms of chemokine receptors and eNOS in Brazilian patients with sickle cell disease.
    Vargas AE; da Silva MA; Silla L; Chies JA
    Tissue Antigens; 2005 Dec; 66(6):683-90. PubMed ID: 16305685
    [TBL] [Abstract][Full Text] [Related]  

  • 74. The presence of alpha-thalassaemia trait blunts the response to hydroxycarbamide in patients with sickle cell disease.
    Vasavda N; Badiger S; Rees D; Height S; Howard J; Thein SL
    Br J Haematol; 2008 Nov; 143(4):589-92. PubMed ID: 18764867
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Beta-globin gene polymorphism in Saudis--triple Hpa I fragments.
    el-Hazmi MA; Jabbar FA; Al-Swailem AR; Warsy AS
    Hum Genet; 1986 Nov; 74(3):313-5. PubMed ID: 2877940
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Sensorineural hearing loss in Nigerian children with sickle cell disease.
    Mgbor N; Emodi I
    Int J Pediatr Otorhinolaryngol; 2004 Nov; 68(11):1413-6. PubMed ID: 15488973
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Determination of sickle hemoglobin polymer in SS and AS erythrocytes.
    Noguchi CT; Torchia DA; Schechter AN
    Blood Cells; 1982; 8(2):225-35. PubMed ID: 7159747
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Hb SE disease: a clinico-hematological profile.
    Mishra P; Pati HP; Chatterjee T; Dixit A; Choudhary DR; Srinivas MU; Mahapatra M; Choudhry VP
    Ann Hematol; 2005 Oct; 84(10):667-70. PubMed ID: 15947927
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Five adults with mild sickle cell anemia share a beta S chromosome with the same haplotype.
    Bakioglu I; Hattori Y; Kutlar A; Mathew C; Huisman TH
    Am J Hematol; 1985 Nov; 20(3):297-300. PubMed ID: 4061450
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Risk factors and prediction of outcomes in children and adolescents who have sickle cell anemia.
    Quinn CT; Miller ST
    Hematol Oncol Clin North Am; 2004 Dec; 18(6):1339-54, ix. PubMed ID: 15511619
    [TBL] [Abstract][Full Text] [Related]  

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