BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 10471465)

  • 21. Update on hereditary hemochromatosis and the HFE gene.
    Brandhagen DJ; Fairbanks VF; Batts KP; Thibodeau SN
    Mayo Clin Proc; 1999 Sep; 74(9):917-21. PubMed ID: 10488796
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Iron beware: a common HFE gene polymorphism may prevent the accurate molecular diagnosis of homozygous hemochromatosis in low-risk, but not high-risk groups.
    Press RD
    Hepatology; 2000 Feb; 31(2):540-2. PubMed ID: 10655286
    [No Abstract]   [Full Text] [Related]  

  • 23. Haemochromatosis: diagnosis and management after the cloning of the HFE gene.
    Powell LW; Bassett ML
    Aust N Z J Med; 1998 Apr; 28(2):159-63. PubMed ID: 9612522
    [No Abstract]   [Full Text] [Related]  

  • 24. HFE genotype in patients with hemochromatosis and other liver diseases.
    McLaren GD
    Ann Intern Med; 2000 Feb; 132(3):245; author reply 246. PubMed ID: 10651611
    [No Abstract]   [Full Text] [Related]  

  • 25. HFE genotype in patients with hemochromatosis and other liver diseases.
    Powell LW
    Ann Intern Med; 2000 Feb; 132(3):245-6. PubMed ID: 10651612
    [No Abstract]   [Full Text] [Related]  

  • 26. Clinical haemochromatosis in HFE mutation carriers.
    Poullis A; Moodie SJ; Maxwell JD
    Lancet; 2002 Aug; 360(9330):411-2; author reply 413-4. PubMed ID: 12241803
    [No Abstract]   [Full Text] [Related]  

  • 27. Haemochromatosis and HLA-H.
    Jouanolle AM; Gandon G; Jézéquel P; Blayau M; Campion ML; Yaouanq J; Mosser J; Fergelot P; Chauvel B; Bouric P; Carn G; Andrieux N; Gicquel I; Le Gall JY; David V
    Nat Genet; 1996 Nov; 14(3):251-2. PubMed ID: 8896550
    [No Abstract]   [Full Text] [Related]  

  • 28. Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.
    de Villiers JN; Scholtz CL; Hoogendijk CF; Cawood EJ; Kotze MJ
    Hum Genet; 1998 Jan; 102(1):127. PubMed ID: 9490291
    [No Abstract]   [Full Text] [Related]  

  • 29. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
    [TBL] [Abstract][Full Text] [Related]  

  • 30. High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.
    Tordai A; Andrikovics H; Kalmár L; Rajczy K; Pénzes M; Sarkadi B; Klein I; Váradi A
    J Med Genet; 1998 Oct; 35(10):878-9. PubMed ID: 9783719
    [No Abstract]   [Full Text] [Related]  

  • 31. [Genetic background and DNA diagnostics of hemochromatosis].
    Heliö T; Färkkilä M; Halme L; Karlsson M; Palotie A; Kontula K
    Duodecim; 1998; 114(14):1404-9. PubMed ID: 11552248
    [No Abstract]   [Full Text] [Related]  

  • 32. Mutations in HFE, the hemochromatosis candidate gene, in patients with NIDDM.
    Dubois-Laforgue D; Caillat-Zucman S; Djilali-Saiah I; Larger E; Mercadier A; Boitard C; Bach JF; Timsit J
    Diabetes Care; 1998 Aug; 21(8):1371-2. PubMed ID: 9702455
    [No Abstract]   [Full Text] [Related]  

  • 33. Haemochromatosis, HFE and genetic complexity.
    Risch N
    Nat Genet; 1997 Dec; 17(4):375-6. PubMed ID: 9398831
    [No Abstract]   [Full Text] [Related]  

  • 34. The significance of the 187G (H63D) mutation in hemochromatosis.
    Beutler E
    Am J Hum Genet; 1997 Sep; 61(3):762-4. PubMed ID: 9326341
    [No Abstract]   [Full Text] [Related]  

  • 35. Screening for hemochromatosis.
    Crawford DH; Hickman P
    Hepatology; 2000 May; 31(5):1192-3. PubMed ID: 10796897
    [No Abstract]   [Full Text] [Related]  

  • 36. Celtic origin of the C282Y mutation of hemochromatosis.
    Lucotte G
    Blood Cells Mol Dis; 1998 Dec; 24(4):433-8. PubMed ID: 9851897
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Haplotype analysis of the HFE gene: implications for the origins of hemochromatosis related mutations.
    Aguilar-Martinez P; Thelcide C; Jeanjean P; Masmejean C; Giansily M; Schved JF
    Blood Cells Mol Dis; 1999; 25(3-4):166-9. PubMed ID: 10575542
    [No Abstract]   [Full Text] [Related]  

  • 38. Mutations of the hereditary hemochromatosis candidate gene HLA-H in porphyria cutanea tarda.
    Santos M; Clevers HC; Marx JJ
    N Engl J Med; 1997 May; 336(18):1327-8. PubMed ID: 9132598
    [No Abstract]   [Full Text] [Related]  

  • 39. Genetic hemochromatosis: why is discovery of the HLA-H gene of interest to rheumatologists?
    Puéchal X
    Rev Rhum Engl Ed; 1997 Oct; 64(10):527-9. PubMed ID: 9385688
    [No Abstract]   [Full Text] [Related]  

  • 40. Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?
    Jouanolle AM; Fergelot P; Raoul ML; Gandon G; Roussey M; Deugnier Y; Feingold J; Le Gall JY; David V
    Ann Genet; 1998; 41(4):195-8. PubMed ID: 9881181
    [TBL] [Abstract][Full Text] [Related]  

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