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 *

153 related articles for article (PubMed ID: 24368960)

  • 1. 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]  

  • 2. Hereditary Hyperferritinemia-Cataract Syndrome in a Family With HFE-H63D Mutation.
    Eris T; Yanik AM; Demirtas D; Yilmaz AF; Toptas T
    Cureus; 2023 Mar; 15(3):e36253. PubMed ID: 37069863
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. [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]  

  • 5. 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]  

  • 6. FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family.
    Ferro E; Capra AP; Zirilli G; Meduri A; Urso M; Briuglia S; La Rosa MA
    Pediatr Dev Pathol; 2018; 21(5):456-460. PubMed ID: 29426274
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families.
    Zin OA; Neves LM; Cunha DP; Motta FL; Agonigi BNS; Horovitz DDG; Almeida DC; Malacarne J; Rodrigues APS; Carvalho AB; Rivello CA; Espariz R; Zin AA; Sallum JMF; Vasconcelos ZFM
    Int J Mol Sci; 2023 Jul; 24(15):. PubMed ID: 37569253
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome.
    Cicilano M; Zecchina G; Roetto A; Bosio S; Infelise V; Stefani S; Mazza U; Camaschella C
    Haematologica; 1999 Jun; 84(6):489-92. PubMed ID: 10366790
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ferritin L-subunit gene mutation and hereditary hyperferritinaemia cataract syndrome (HHCS): a case report and literature review.
    Yang Y; Lin T; Kuang P; Chen X
    Hematology; 2021 Dec; 26(1):896-903. PubMed ID: 34789084
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Analysis of ferritins in lymphoblastoid cell lines and in the lens of subjects with hereditary hyperferritinemia-cataract syndrome.
    Levi S; Girelli D; Perrone F; Pasti M; Beaumont C; Corrocher R; Albertini A; Arosio P
    Blood; 1998 Jun; 91(11):4180-7. PubMed ID: 9596665
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA.
    Cazzola M; Bergamaschi G; Tonon L; Arbustini E; Grasso M; Vercesi E; Barosi G; Bianchi PE; Cairo G; Arosio P
    Blood; 1997 Jul; 90(2):814-21. PubMed ID: 9226182
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.