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Journal Abstract Search


118 related items for PubMed ID: 10211896

  • 1. Elevated parathyroid hormone 44-68 and osteoarticular changes in patients with genetic hemochromatosis.
    Pawlotsky Y, Le Dantec P, Moirand R, Guggenbuhl P, Jouanolle AM, Catheline M, Meadeb J, Brissot P, Deugnier Y, Chalès G.
    Arthritis Rheum; 1999 Apr; 42(4):799-806. PubMed ID: 10211896
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  • 2. Elevated parathyroid hormone 44-68 in idiopathic calcium pyrophosphate dihydrate crystal deposition disease. Role of menopause and iron metabolism?
    Pawlotsky Y, Massart C, Guggenbuhl P, Albert JD, Perdriger A, Meadeb J, Chalès G.
    J Rheumatol; 2008 Feb; 35(2):315-8. PubMed ID: 18061978
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  • 3. Hepatic and serum ferritin concentrations in patients with idiopathic hemochromatosis.
    Beaumont C, Simon M, Smith PM, Worwood M.
    Gastroenterology; 1980 Nov; 79(5 Pt 1):877-83. PubMed ID: 7419012
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  • 4. Familial hemochromatosis. Physiologic studies in the precirrhotic stage of the disease.
    Feller ER, Pont A, Wands JR, Carter EA, Foster G, Kourides IA, Isselbacher KJ.
    N Engl J Med; 1977 Jun 23; 296(25):1422-6. PubMed ID: 194151
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  • 5. [Iron balance in hemodialysis in chronic uremia].
    Kokot F, Warmuz A.
    Z Urol Nephrol; 1988 Apr 23; 81(4):263-8. PubMed ID: 3400353
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  • 7. Screening for hemochromatosis in asymptomatic subjects with or without a family history.
    Powell LW, Dixon JL, Ramm GA, Purdie DM, Lincoln DJ, Anderson GJ, Subramaniam VN, Hewett DG, Searle JW, Fletcher LM, Crawford DH, Rodgers H, Allen KJ, Cavanaugh JA, Bassett ML.
    Arch Intern Med; 2006 Feb 13; 166(3):294-301. PubMed ID: 16476869
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  • 9. The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis.
    Adams PC, Deugnier Y, Moirand R, Brissot P.
    Hepatology; 1997 Jan 13; 25(1):162-6. PubMed ID: 8985284
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  • 11. Assessment of silent liver fibrosis in hemochromatosis C282Y homozygotes with normal transaminase levels.
    Beaton M, Adams PC.
    Clin Gastroenterol Hepatol; 2008 Jun 13; 6(6):713-4. PubMed ID: 18550006
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  • 14. Influence of sevelamer hydrochloride on serum concentration of whole (1-84) and N-terminally truncated (7-84) parathyroid hormone fragments in hemodialysis uremic patients.
    Chudek J, Piecha G, Kokot F, Wiecek A.
    J Nephrol; 2003 Jun 13; 16(5):710-5. PubMed ID: 14733418
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  • 16. Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.
    Majore S, Milano F, Binni F, Stuppia L, Cerrone A, Tafuri A, De Bernardo C, Palka G, Grammatico P.
    Haematologica; 2006 Aug 13; 91(8 Suppl):ECR33. PubMed ID: 16923517
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  • 20. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
    de Diego C, Opazo S, Murga MJ, Martínez-Castro P.
    Eur J Haematol; 2007 Jan 13; 78(1):66-71. PubMed ID: 17042772
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