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136 related items for PubMed ID: 12010659

  • 21. HFE gene mutation and iron overload in Egyptian pediatric acute lymphoblastic leukemia survivors: a single-center study.
    El-Rashedi FH, El-Hawy MA, El-Hefnawy SM, Mohammed MM.
    Hematology; 2017 Aug; 22(7):398-404. PubMed ID: 28211293
    [Abstract] [Full Text] [Related]

  • 22. TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy.
    Radio FC, Majore S, Binni F, Valiante M, Ricerca BM, De Bernardo C, Morrone A, Grammatico P.
    Blood Cells Mol Dis; 2014 Aug; 52(2-3):83-7. PubMed ID: 24055163
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  • 25. Population-based screening for hemochromatosis using phenotypic and DNA testing among employees of health maintenance organizations in Springfield, Missouri.
    McDonnell SM, Hover A, Gloe D, Ou CY, Cogswell ME, Grummer-Strawn L.
    Am J Med; 1999 Jul; 107(1):30-7. PubMed ID: 10403350
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  • 27. Identification of hemochromatosis gene polymorphisms in chronically transfused patients with sickle cell disease.
    Jeng MR, Adams-Graves P, Howard TA, Whorton MR, Li CS, Ware RE.
    Am J Hematol; 2003 Dec; 74(4):243-8. PubMed ID: 14635204
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  • 28. Prevalence of idiopathic hemochromatosis in Italy: study of 1301 blood donors.
    Velati C, Piperno A, Fargion S, Colombo S, Fiorelli G.
    Haematologica; 1990 Dec; 75(4):309-12. PubMed ID: 2276675
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  • 29. Biochemical expression of heterozygous hereditary hemochromatosis.
    de Valk B, Witlox RS, van der Schouw YT, Marx JJ.
    Eur J Intern Med; 2000 Dec 20; 11(6):317-321. PubMed ID: 11113655
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  • 30. Two novel nonsense mutations of HFE gene in five unrelated italian patients with hemochromatosis.
    Piperno A, Arosio C, Fossati L, Viganò M, Trombini P, Vergani A, Mancia G.
    Gastroenterology; 2000 Aug 20; 119(2):441-5. PubMed ID: 10930379
    [Abstract] [Full Text] [Related]

  • 31. Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia.
    Zekavat OR, Zareian Jahromi M, Haghpanah S, Kargar Jahromi Z, Cohan N.
    J Pediatr Hematol Oncol; 2021 Jan 20; 43(1):e26-e28. PubMed ID: 32925401
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  • 32. Influence of iron regulating genes mutations on iron status in Egyptian patients with sickle cell disease.
    Abdel Rahman HA, Abou-Elew HH, El-Shorbagy RM, Fawzy R, Youssry I.
    Ann Clin Lab Sci; 2014 Jan 20; 44(3):304-9. PubMed ID: 25117103
    [Abstract] [Full Text] [Related]

  • 33. Classification and diagnosis of iron overload.
    Piperno A.
    Haematologica; 1998 May 20; 83(5):447-55. PubMed ID: 9658731
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  • 34. Iron overload in Africa. Interaction between a gene and dietary iron content.
    Gordeuk V, Mukiibi J, Hasstedt SJ, Samowitz W, Edwards CQ, West G, Ndambire S, Emmanual J, Nkanza N, Chapanduka Z.
    N Engl J Med; 1992 Jan 09; 326(2):95-100. PubMed ID: 1727237
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  • 35. Mass spectrometry measurement of plasma hepcidin for the prediction of iron overload.
    Floreani A, Navaglia F, Rizzotto ER, Basso D, Chiaramonte M, Padoan A, Petridis I, Cazzagon N, Testa R, Marra M, Plebani M.
    Clin Chem Lab Med; 2011 Feb 09; 49(2):197-206. PubMed ID: 21143008
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  • 36. Molecular diagnosis of genetic iron-overload disorders.
    Brissot P, Bardou-Jacquet E, Troadec MB, Mosser A, Island ML, Detivaud L, Loréal O, Jouanolle AM.
    Expert Rev Mol Diagn; 2010 Sep 09; 10(6):755-63. PubMed ID: 20843199
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  • 37. [Iron overload and cancer].
    Blanc JF, Bioulac-Sage P, Balabaud C.
    Bull Acad Natl Med; 2000 Sep 09; 184(2):355-63. PubMed ID: 10989544
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  • 38. HFE gene mutation and oxidative damage biomarkers in patients with myelodysplastic syndromes and its relation to transfusional iron overload: an observational cross-sectional study.
    De Souza GF, Ribeiro HL, De Sousa JC, Heredia FF, De Freitas RM, Martins MR, Gonçalves RP, Pinheiro RF, Magalhães SM.
    BMJ Open; 2015 Apr 03; 5(4):e006048. PubMed ID: 25841232
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  • 39. C282Y/H63D Compound Heterozygosity Is a Low Penetrance Genotype for Iron Overload-related Disease.
    Hasan SMM, Farrell J, Borgaonkar M.
    J Can Assoc Gastroenterol; 2022 Oct 03; 5(5):240-247. PubMed ID: 36196271
    [Abstract] [Full Text] [Related]

  • 40. HFE-associated hereditary hemochromatosis: overview of genetics and clinical implications for nurse practitioners in primary care settings.
    Emanuele D, Tuason I, Edwards QT.
    J Am Assoc Nurse Pract; 2014 Mar 03; 26(3):113-22. PubMed ID: 24574363
    [Abstract] [Full Text] [Related]

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