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 *

185 related articles for article (PubMed ID: 15234655)

  • 41. A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome.
    Aguilar-Martinez P; Biron C; Masmejean C; Jeanjean P; Schved JF
    Blood; 1996 Sep; 88(5):1895. PubMed ID: 8781450
    [No Abstract]   [Full Text] [Related]  

  • 42. Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family.
    Cosentino I; Zeri F; Swann PG; Majore S; Radio FC; Palumbo P; Grammatico P; Petitti V
    Ophthalmic Genet; 2016 Sep; 37(3):318-22. PubMed ID: 26849797
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations.
    Craig JE; Clark JB; McLeod JL; Kirkland MA; Grant G; Elder JE; Toohey MG; Kowal L; Savoia HF; Chen C; Roberts S; Wirth MG; Mackey DA
    Arch Ophthalmol; 2003 Dec; 121(12):1753-61. PubMed ID: 14662596
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Hyperferritinaemia in the absence of iron overload.
    Arnold JD; Mumford AD; Lindsay JO; Hegde U; Hagan M; Hawkins JR
    Gut; 1997 Sep; 41(3):408-10. PubMed ID: 9378401
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. 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]  

  • 47. Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases.
    Celma Nos F; Hernández G; Ferrer-Cortès X; Hernandez-Rodriguez I; Navarro-Almenzar B; Fuster JL; Bermúdez Cortés M; Pérez-Montero S; Tornador C; Sanchez M
    Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34064225
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Hereditary hyperferritinaemia cataract syndrome: does it exist in Switzerland?
    Rosochova J; Kapetanios A; Pournaras C; Vadas L; Samii K; Beris P
    Schweiz Med Wochenschr; 2000 Mar; 130(9):324-8. PubMed ID: 10746272
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A novel double nucleotide variant in the ferritin-L iron-responsive element in a Finnish patient with hereditary hyperferritinaemia-cataract syndrome.
    Mattila RM; Sainio A; Järveläinen M; Pursiheimo J; Järveläinen H
    Acta Ophthalmol; 2018 Feb; 96(1):95-99. PubMed ID: 28636169
    [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. 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]  

  • 53. A novel deletion of the L-ferritin iron-responsive element responsible for severe hereditary hyperferritinaemia-cataract syndrome.
    Cazzola M; Foglieni B; Bergamaschi G; Levi S; Lazzarino M; Arosio P
    Br J Haematol; 2002 Mar; 116(3):667-70. PubMed ID: 11849230
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Prevalence of hereditary hyperferritinemia-cataract syndrome in blood donors and patients with cataract.
    Bozzini C; Galbiati S; Tinazzi E; Aldigeri R; De Matteis G; Girelli D
    Haematologica; 2003 Feb; 88(2):219-20. PubMed ID: 12604412
    [No Abstract]   [Full Text] [Related]  

  • 55. The case of a 1-year-old girl with hereditary hyperferritinemia cataract syndrome.
    Rochow N; Bachmaier N; Tost F; Beck JF; Bernig T
    Pediatr Hematol Oncol; 2009; 26(3):136-41. PubMed ID: 19382035
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Gene symbol: FTL. Disease: Hyperferritinemia-cataract syndrome.
    Piperno A; Pelucchi S
    Hum Genet; 2004 Mar; 114(4):406. PubMed ID: 15046083
    [No Abstract]   [Full Text] [Related]  

  • 57. [Genetics of iron overloads and hereditary hyperferritinemia cataract syndrome].
    García-Erce JA; Salvador Osuna C
    An Med Interna; 2003 Apr; 20(4):213-4. PubMed ID: 12768838
    [No Abstract]   [Full Text] [Related]  

  • 58. Raised serum ferritin concentration in hereditary hyperferritinemia cataract syndrome is not a marker for iron overload.
    Yin D; Kulhalli V; Walker AP
    Hepatology; 2014 Mar; 59(3):1204-6. PubMed ID: 24003015
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Pair of siblings of Italian ethnicity with hyperferritinemia and cataract].
    Volkmann M; Schiff JH; Hör M; Hentze MW; Fiehn W; Merkt J
    Internist (Berl); 2000 Apr; 41(4):381-4. PubMed ID: 10798187
    [No Abstract]   [Full Text] [Related]  

  • 60. The hereditary hyperferritinemia-cataract syndrome: a family study.
    Álvarez-Coca-González J; Moreno-Carralero MI; Martínez-Pérez J; Méndez M; García-Ros M; Morán-Jiménez MJ
    Eur J Pediatr; 2010 Dec; 169(12):1553-5. PubMed ID: 20617342
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.