BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

273 related articles for article (PubMed ID: 16900584)

  • 21. Dual diagnoses of hereditary hyperferritinaemia-cataract syndrome and hereditary haemochromatosis.
    Hughes M; Vosylius P
    Clin Lab Haematol; 2006 Oct; 28(5):357-9. PubMed ID: 16999731
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hemochromatosis and iron-overload screening in a racially diverse population.
    Adams PC; Reboussin DM; Barton JC; McLaren CE; Eckfeldt JH; McLaren GD; Dawkins FW; Acton RT; Harris EL; Gordeuk VR; Leiendecker-Foster C; Speechley M; Snively BM; Holup JL; Thomson E; Sholinsky P;
    N Engl J Med; 2005 Apr; 352(17):1769-78. PubMed ID: 15858186
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit gene.
    Girelli D; Corrocher R; Bisceglia L; Olivieri O; Zelante L; Panozzo G; Gasparini P
    Blood; 1997 Sep; 90(5):2084-8. PubMed ID: 9292547
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A case report of spontaneous mutation (C33>U) in the iron-responsive element of L-ferritin causing hyperferritinemia-cataract syndrome.
    Cao W; McMahon M; Wang B; O'Connor R; Clarkson M
    Blood Cells Mol Dis; 2010 Jan; 44(1):22-7. PubMed ID: 19800271
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of a novel mutation in the L-ferritin IRE leading to hereditary hyperferritinemia-cataract syndrome.
    Phillips JD; Warby CA; Kushner JP
    Am J Med Genet A; 2005 Apr; 134A(1):77-9. PubMed ID: 15690351
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IRE.
    Papanikolaou G; Chandrinou H; Bouzas E; Contopoulos-Ioannidis D; Kalotychou V; Prentzas K; Lilakos K; Asproudis I; Palaiologou D; Premetis E; Papassotiriou I; Sakellaropoulos N
    Blood Cells Mol Dis; 2006; 36(1):33-40. PubMed ID: 16406710
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Reference centiles for serum ferritin and percentage of transferrin saturation, with application to mutations of the HFE gene.
    Koziol JA; Ho NJ; Felitti VJ; Beutler E
    Clin Chem; 2001 Oct; 47(10):1804-10. PubMed ID: 11568090
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A point mutation in the iron-responsive element of the L-ferritin in a family with hereditary hyperferritinemia cataract syndrome.
    Wong K; Barbin Y; Chakrabarti S; Adams P
    Can J Gastroenterol; 2005 Apr; 19(4):253-5. PubMed ID: 15861269
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Population screening for hemochromatosis: a study in 5370 Spanish blood donors.
    Sánchez M; Villa M; Ingelmo M; Sanz C; Bruguera M; Ascaso C; Oliva R
    J Hepatol; 2003 Jun; 38(6):745-50. PubMed ID: 12763366
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
    Nie L; Ai XF; Zheng YZ; Li QH; Yang L; Xiao ZJ
    Zhonghua Xue Ye Xue Za Zhi; 2009 Apr; 30(4):223-8. PubMed ID: 19731820
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Aqueous humor ferritin in hereditary hyperferritinemia cataract syndrome.
    Lenzhofer M; Schroedl F; Trost A; Kaser-Eichberger A; Wiedemann H; Strohmaier C; Hohensinn M; Strasser M; Muckenthaler MU; Grabner G; Aigner E; Reitsamer HA
    Optom Vis Sci; 2015 Apr; 92(4 Suppl 1):S40-7. PubMed ID: 25756341
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene.
    Silva B; Pita L; Gomes S; Gonçalves J; Faustino P
    Ann Hematol; 2014 Dec; 93(12):2063-6. PubMed ID: 25015054
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hereditary hyperferritinaemia-cataract syndrome: a challenging diagnosis for the hepatogastroenterologist.
    Ferrante M; Geubel AP; Fevery J; Marogy G; Horsmans Y; Nevens F
    Eur J Gastroenterol Hepatol; 2005 Nov; 17(11):1247-53. PubMed ID: 16215440
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hyperferritinemia, iron overload, and multiple metabolic alterations identify patients at risk for nonalcoholic steatohepatitis.
    Fargion S; Mattioli M; Fracanzani AL; Sampietro M; Tavazzi D; Fociani P; Taioli E; Valenti L; Fiorelli G
    Am J Gastroenterol; 2001 Aug; 96(8):2448-55. PubMed ID: 11513189
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Iron status and HFE genotype in erythrocyte pyruvate kinase deficiency: study of Italian cases.
    Zanella A; Bianchi P; Iurlo A; Boschetti C; Taioli E; Vercellati C; Zappa M; Fermo E; Tavazzi D; Sampietro M
    Blood Cells Mol Dis; 2001; 27(3):653-61. PubMed ID: 11482880
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hyperferritinemia and iron overload in type 1 Gaucher disease.
    Stein P; Yu H; Jain D; Mistry PK
    Am J Hematol; 2010 Jul; 85(7):472-6. PubMed ID: 20575041
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The hereditary hyperferritinemia-cataract syndrome in 2 italian families.
    Perruccio K; Arcioni F; Cerri C; La Starza R; Romanelli D; Capolsini I; Caniglia M
    Case Rep Pediatr; 2013; 2013():806034. PubMed ID: 24368960
    [TBL] [Abstract][Full Text] [Related]  

  • 39. HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants.
    Barton JC; Lafreniere SA; Leiendecker-Foster C; Li H; Acton RT; Press RD; Eckfeldt JH
    Am J Hematol; 2009 Nov; 84(11):710-4. PubMed ID: 19787796
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hereditary hyperferritinemia cataract syndrome: clinical, genetic, and laboratory findings in 5 families.
    Nonnenmacher L; Langer T; Blessing H; Gabriel H; Buchwald HJ; Meneksedag C; Kohne E; Gencik M; Debatin KM; Cario H
    Klin Padiatr; 2011 Nov; 223(6):346-51. PubMed ID: 22020773
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.