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 *

203 related articles for article (PubMed ID: 15842597)

  • 21. Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations.
    Hetet G; Devaux I; Soufir N; Grandchamp B; Beaumont C
    Blood; 2003 Sep; 102(5):1904-10. PubMed ID: 12730114
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Iron stores modulate hepatic hepcidin expression by an HFE-independent pathway.
    Gehrke SG; Herrmann T; Kulaksiz H; Merle U; Bents K; Kaiser I; Riedel HD; Stremmel W
    Digestion; 2005; 72(1):25-32. PubMed ID: 16103673
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetic background of primary iron overload syndromes in Japan.
    Hayashi H; Wakusawa S; Motonishi S; Miyamoto K; Okada H; Inagaki Y; Ikeda T
    Intern Med; 2006; 45(20):1107-11. PubMed ID: 17106152
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Relative contribution of iron genes, dysmetabolism and hepatitis C virus (HCV) in the pathogenesis of altered iron regulation in HCV chronic hepatitis.
    Valenti L; Pulixi EA; Arosio P; Cremonesi L; Biasiotto G; Dongiovanni P; Maggioni M; Fargion S; Fracanzani AL
    Haematologica; 2007 Aug; 92(8):1037-42. PubMed ID: 17640859
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Juvenile hemochromatosis associated with heterozygosity for novel hemojuvelin mutations and with unknown cofactors.
    Pelusi S; Rametta R; Della Corte C; Congia R; Dongiovanni P; Pulixi EA; Fargion S; Fracanzani AL; Nobili V; Valenti L
    Ann Hepatol; 2014; 13(5):568-71. PubMed ID: 25152992
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Early age-of-onset iron overload and homozygosity for the novel hemojuvelin mutation HJV R54X (exon 3; c.160A-->T) in an African American male of West Indies descent.
    Murugan RC; Lee PL; Kalavar MR; Barton JC
    Clin Genet; 2008 Jul; 74(1):88-92. PubMed ID: 18492090
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The ferroportin disease.
    Pietrangelo A
    Blood Cells Mol Dis; 2004; 32(1):131-8. PubMed ID: 14757427
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Inherited Disorders of Iron Overload.
    Pantopoulos K
    Front Nutr; 2018; 5():103. PubMed ID: 30420953
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Ferroportin disease: a systematic meta-analysis of clinical and molecular findings.
    Mayr R; Janecke AR; Schranz M; Griffiths WJ; Vogel W; Pietrangelo A; Zoller H
    J Hepatol; 2010 Nov; 53(5):941-9. PubMed ID: 20691492
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes.
    Pietrangelo A; Caleffi A; Henrion J; Ferrara F; Corradini E; Kulaksiz H; Stremmel W; Andreone P; Garuti C
    Gastroenterology; 2005 Feb; 128(2):470-9. PubMed ID: 15685557
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Inherited iron loading: genetic testing in diagnosis and management.
    Worwood M
    Blood Rev; 2005 Mar; 19(2):69-88. PubMed ID: 15603911
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A diagnostic approach to hyperferritinemia with a non-elevated transferrin saturation.
    Adams PC; Barton JC
    J Hepatol; 2011 Aug; 55(2):453-8. PubMed ID: 21354228
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Pathophysiology and genetics of classic HFE (type 1) hemochromatosis].
    Loréal O; Ropert M; Mosser A; Déhais V; Deugnier Y; David V; Brissot P; Jouanolle AM
    Presse Med; 2007 Sep; 36(9 Pt 2):1271-7. PubMed ID: 17521857
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hereditary iron overload: update on pathophysiology, diagnosis, and treatment.
    Franchini M
    Am J Hematol; 2006 Mar; 81(3):202-9. PubMed ID: 16493621
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of new mutations of the HFE, hepcidin, and transferrin receptor 2 genes by denaturing HPLC analysis of individuals with biochemical indications of iron overload.
    Biasiotto G; Belloli S; Ruggeri G; Zanella I; Gerardi G; Corrado M; Gobbi E; Albertini A; Arosio P
    Clin Chem; 2003 Dec; 49(12):1981-8. PubMed ID: 14633868
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Hereditary hyperferritinemia cataract syndrome].
    Holzgreve H
    Dtsch Med Wochenschr; 2011 Sep; 136(38):1895-8. PubMed ID: 21915803
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Rare types of genetic hemochromatosis.
    Camaschella C; Poggiali E
    Acta Haematol; 2009; 122(2-3):140-5. PubMed ID: 19907151
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron.
    Koyama C; Wakusawa S; Hayashi H; Ueno T; Suzuki R; Yano M; Saito H; Okazaki T
    Intern Med; 2005 Sep; 44(9):990-3. PubMed ID: 16258219
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Hyperferritinemia, ferropenia and metabolic syndrome in a patient with a new mutation of gene TFR2 and another in gene FTL. A family study].
    Del Castillo-Rueda A; Moreno-Carralero MI; Cuadrado-Grande N; Méndez M; Morán-Jiménez MJ
    Med Clin (Barc); 2011 Jun; 137(2):68-72. PubMed ID: 21524769
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A new family with hereditary hyperferritinemia cataract syndrome.
    Tuysuz G; Ozdemir N; Sonmez E; Kannengiesser C; Celkan T
    Genet Couns; 2013; 24(4):393-7. PubMed ID: 24551982
    [TBL] [Abstract][Full Text] [Related]  

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