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 *

140 related articles for article (PubMed ID: 10383191)

  • 21. Hyperferritinaemia-cataract syndrome.
    Lindberg K; Hellebostad M
    Acta Ophthalmol Scand; 1999 Aug; 77(4):478-80. PubMed ID: 10463429
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [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]  

  • 23. Hereditary hyperferritinemia-cataract syndrome: two novel mutations in the L-ferritin iron-responsive element.
    Mumford AD; Vulliamy T; Lindsay J; Watson A
    Blood; 1998 Jan; 91(1):367-8. PubMed ID: 9414313
    [No Abstract]   [Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. Identification of a novel mutation in the L ferritin iron-responsive element causing hereditary hyperferritinemia-cataract syndrome.
    Messa E; Pellegrino RM; Palmieri A; Carturan S; Cilloni D; Saglio G; Roetto A
    Acta Haematol; 2009; 122(4):223-5. PubMed ID: 19887780
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. [Molecular genetics of hereditary cataract-hyperferritinemia syndrome].
    Milon B; Beaumont C
    Ann Biol Clin (Paris); 1998 Jul; 56 Spec No():36-40. PubMed ID: 9827213
    [No Abstract]   [Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. 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]  

  • 37. Ferritin light chain gene mutations in two Brazilian families with hereditary hyperferritinemia-cataract syndrome.
    Petroni RC; Rosa SEAD; Carvalho FP; Santana RAF; Hyppolito JE; Nascimento CMDB; Hamerschlak N; Campregher PV
    Einstein (Sao Paulo); 2017; 15(4):492-495. PubMed ID: 28746593
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.