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 *

303 related articles for article (PubMed ID: 14662596)

  • 1. 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]  

  • 2. Ferritin crystal cataracts in hereditary hyperferritinemia cataract syndrome.
    Brooks DG; Manova-Todorova K; Farmer J; Lobmayr L; Wilson RB; Eagle RC; St Pierre TG; Stambolian D
    Invest Ophthalmol Vis Sci; 2002 Apr; 43(4):1121-6. PubMed ID: 11923255
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Lens changes in hereditary hyperferritinemia-cataract syndrome.
    Chang-Godinich A; Ades S; Schenkein D; Brooks D; Stambolian D; Raizman MB
    Am J Ophthalmol; 2001 Nov; 132(5):786-8. PubMed ID: 11704046
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Hereditary hyperferritinemia-cataract syndrome in two large multigenerational American families.
    Shekunov J; de Groen PC; Lindor NM; Klee GG; Aleff RA; Wieben ED; Mohney BG
    J AAPOS; 2011 Aug; 15(4):356-61. PubMed ID: 21907119
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Hereditary hyperferritinemia cataracts syndrome in a Spanish family caused by the A40G mutation (Paris) in the L-ferritin (FTL) gene associated with the mutation H63D in the HFE gene].
    Del Castillo Rueda A; Fernández Ruano ML
    Med Clin (Barc); 2007 Sep; 129(11):414-7. PubMed ID: 17927936
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary hyperferritinemia-cataract syndrome.
    Christiansen G; Mohney BG
    J AAPOS; 2007 Jun; 11(3):294-6. PubMed ID: 17572344
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia.
    Tsantoula F; Kioumi A; Germenis AE; Speletas M
    J Pediatr Hematol Oncol; 2014 Jul; 36(5):e304-6. PubMed ID: 24983587
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. [Hyperferritinemia-cataract syndrome associated to the HFE gene mutation. Two new Spanish families and a new mutation (A37T: "Zaragoza")].
    García Erce JA; Cortés T; Cremonesi L; Cazzola M; Pérez-Lungmus G; Giralt M
    Med Clin (Barc); 2006 Jun; 127(2):55-8. PubMed ID: 16900584
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hereditary hyperferritinaemia-cataract syndrome].
    van der Klooster JM
    Ned Tijdschr Geneeskd; 2003 Sep; 147(39):1923-8. PubMed ID: 14560693
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. [Hereditary hyperferritinemia cataract syndrome--the first family in Germany].
    Millonig G; Holzer MP; Tolle G; Auffarth GU; Muckenthaler MU; Seitz HK; Mueller S
    Z Gastroenterol; 2009 Dec; 47(12):1211. PubMed ID: 19994473
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary hyperferritinemia-cataract syndrome (HHCS) presenting with iron deficiency anemia associated with a new mutation in the iron responsive element of the L ferritin gene in a Swiss family.
    Rüfer A; Howell JP; Lange AP; Yamamoto R; Heuscher J; Gregor M; Wuillemin WA
    Eur J Haematol; 2011 Sep; 87(3):274-8. PubMed ID: 21410535
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.