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 *

125 related articles for article (PubMed ID: 24022025)

  • 1. [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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Homozygous mutation of the 5'UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype.
    Giansily-Blaizot M; Cunat S; Moulis G; Schved JF; Aguilar-Martinez P
    Haematologica; 2013 Apr; 98(4):e42-3. PubMed ID: 23300176
    [No Abstract]   [Full Text] [Related]  

  • 5. [Isolated hyperferritinemia in a healthy male infant: hereditary hyperferritinemia-cataract syndrome].
    Cervera Bravo A; Sebastían Planas M; Alarabe Alarabe A; Díez Sáenz A; Avilés Egea MJ; Balas Pérez A
    An Esp Pediatr; 2000 Mar; 52(3):267-70. PubMed ID: 11003906
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Hereditary hyperferritinemia cataract syndrome: a de novo mutation in the iron responsive element of the L-ferritin gene.
    Arosio C; Fossati L; Viganò M; Trombini P; Cazzaniga G; Piperno A
    Haematologica; 1999 Jun; 84(6):560-1. PubMed ID: 10366804
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Description of a new mutation in the L-ferrin iron-responsive element associated with hereditary hyperferritinemia-cataract syndrome in a Spanish family.
    Balas A; Aviles MJ; Garcia-Sanchez F; Vicario JL
    Blood; 1999 Jun; 93(11):4020-1. PubMed ID: 10383191
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy.
    Pallotti F; Elli L; Maroni P; Chelazzi P; Agosti M; Casalone R
    Clin Chem Lab Med; 2015 Sep; 53(10):e275-7. PubMed ID: 25720123
    [No Abstract]   [Full Text] [Related]  

  • 14. Hereditary hyperferritinemia cataract syndrome in four patients with mutations in the IRE of the FTL gene.
    Muñoz-Muñoz J; Cuadrado-Grande N; Moreno-Carralero MI; Hoyos-Sanabria B; Manubes-Guarch A; González AF; Tejada-Palacios P; Del-Castillo-Rueda A; Morán-Jiménez MJ
    Clin Genet; 2013 May; 83(5):491-3. PubMed ID: 22881709
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. [Hyperferritinemia, ferropenia and metabolic syndrome in a patient with a new mutation of gene TFR2 and another in gene FTL. A family study].
    Del Castillo-Rueda A; Moreno-Carralero MI; Cuadrado-Grande N; Méndez M; Morán-Jiménez MJ
    Med Clin (Barc); 2011 Jun; 137(2):68-72. PubMed ID: 21524769
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel deletion in the iron-response element of the L-ferritin gene, causing hyperferritinaemia cataract syndrome.
    Garber I; Pudek M
    Ann Clin Biochem; 2014 Nov; 51(Pt 6):710-3. PubMed ID: 24936091
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

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

    [Next]    [New Search]
    of 7.