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 *

105 related articles for article (PubMed ID: 8639868)

  • 41. 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]  

  • 42. Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract.
    Beaumont C; Leneuve P; Devaux I; Scoazec JY; Berthier M; Loiseau MN; Grandchamp B; Bonneau D
    Nat Genet; 1995 Dec; 11(4):444-6. PubMed ID: 7493028
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Two Dutch families with hereditary hyperferritinaemia-cataract syndrome and heterozygosity for an HFE-related haemochromatosis gene mutation.
    Simsek S; Nanayakkara PW; Keek JM; Faber LM; Bruin KF; Pals G
    Neth J Med; 2003 Sep; 61(9):291-5. PubMed ID: 14692443
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Hereditary hyperferritinemia and cataract syndrome: a de novo mutation].
    Hernández Martín D; Cervera Bravo A; Balas Pérez A
    An Pediatr (Barc); 2008 Apr; 68(4):408-10. PubMed ID: 18394394
    [No Abstract]   [Full Text] [Related]  

  • 45. [New mutation in a Spanish family with hereditary hyperferritinemia-cataract syndrome].
    Santotoribio JD; García de la Torre Á; Cañavate Solano C; Toral Peña A
    Med Clin (Barc); 2014 Jan; 142(2):93. PubMed ID: 24022025
    [No Abstract]   [Full Text] [Related]  

  • 46. [Hereditary hyperferritinemia syndrome and cataract].
    Feys J; Nodarian M; Aygalenq P; Cattan D; Bouccara AS; Beaumont C
    J Fr Ophtalmol; 2001 Oct; 24(8):847-50. PubMed ID: 11894536
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Hereditary hyperferritinaemia/ cataract syndrome.
    Cazzola M
    Best Pract Res Clin Haematol; 2002 Jun; 15(2):385-98. PubMed ID: 12401313
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Hereditary hyperferritinemia cataract syndrome: ocular, genetic, and biochemical findings.
    Ismail AR; Lachlan KL; Mumford AD; Temple IK; Hodgkins PR
    Eur J Ophthalmol; 2006; 16(1):153-60. PubMed ID: 16496261
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Hereditary hyperferritinaemia-cataract syndrome].
    Simsek S; Nanayakkara PW
    Ned Tijdschr Geneeskd; 2003 Dec; 147(51):2557; author reply 2557-8. PubMed ID: 14735856
    [No Abstract]   [Full Text] [Related]  

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

  • 52. A family with hereditary hyperferritinaemia cataract syndrome: evidence of incomplete penetrance and clinical heterogeneity.
    Gonzalez-Huerta L; Ramirez-Sanchez V; Rivera-Vega M; Messina-Baas O; Cuevas-Covarrubias S
    Br J Haematol; 2008 Nov; 143(4):596-8. PubMed ID: 18710380
    [No Abstract]   [Full Text] [Related]  

  • 53. [Hereditary hyperferritinemia-cataract syndrome].
    Merkt J
    Dtsch Med Wochenschr; 1997 Apr; 122(16):504-6. PubMed ID: 9162623
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site.
    Burdon KP; Sharma S; Chen CS; Dimasi DP; Mackey DA; Craig JE
    Hum Mutat; 2007 Jul; 28(7):742. PubMed ID: 17579362
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. Assignment of ferritin L gene (FTL) to human chromosome band 19q13.3 by in situ hybridization.
    Gasparini P; Calvano S; Memeo E; Bisceglia L; Zelante L
    Ann Genet; 1997; 40(4):227-8. PubMed ID: 9526618
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Congenital cataract syndrome and hyperferritinemia].
    García-Erce JA; Salvador-Osuna C; Cortés T; Pérez-Lungmus G
    Med Clin (Barc); 1999 Mar; 112(10):398. PubMed ID: 10227023
    [No Abstract]   [Full Text] [Related]  

  • 59. Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin.
    Vanita V; Hejtmancik JF; Hennies HC; Guleria K; Nürnberg P; Singh D; Sperling K; Singh JR
    Mol Vis; 2006 Feb; 12():93-9. PubMed ID: 16518306
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Identification of the mutations associated with hereditary hyperferritinemia cataract syndrome and hemochromatosis in a Brazilian family.
    Meneses FG; Schnabel B; Silva ID; Alberto FL; Toma L; Nader HB; Lopes CC
    Clin Genet; 2011 Feb; 79(2):189-92. PubMed ID: 21210779
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.