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 *

210 related articles for article (PubMed ID: 15861269)

  • 41. 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]  

  • 42. Clinical severity and thermodynamic effects of iron-responsive element mutations in hereditary hyperferritinemia-cataract syndrome.
    Allerson CR; Cazzola M; Rouault TA
    J Biol Chem; 1999 Sep; 274(37):26439-47. PubMed ID: 10473603
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract.
    Bennett TM; Maraini G; Jin C; Sun W; Hejtmancik JF; Shiels A
    Mol Vis; 2013; 19():835-44. PubMed ID: 23592921
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload.
    Kannengiesser C; Jouanolle AM; Hetet G; Mosser A; Muzeau F; Henry D; Bardou-Jacquet E; Mornet M; Brissot P; Deugnier Y; Grandchamp B; Beaumont C
    Haematologica; 2009 Mar; 94(3):335-9. PubMed ID: 19176363
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [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]  

  • 46. 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]  

  • 47. 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]  

  • 48. 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]  

  • 49. Mutation spectrum in Australian pedigrees with hereditary hyperferritinaemia-cataract syndrome reveals novel and de novo mutations.
    McLeod JL; Craig J; Gumley S; Roberts S; Kirkland MA
    Br J Haematol; 2002 Sep; 118(4):1179-82. PubMed ID: 12199804
    [TBL] [Abstract][Full Text] [Related]  

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

  • 51. 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]  

  • 52. Onset of cataract in early infancy associated with a 32G-->C transition in the iron responsive element of L-ferritin.
    Campagnoli MF; Pimazzoni R; Bosio S; Zecchina G; DeGobbi M; Bosso P; Oldani B; Ramenghi U
    Eur J Pediatr; 2002 Sep; 161(9):499-502. PubMed ID: 12200611
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. Clinical features and molecular analysis of seven British kindreds with hereditary hyperferritinaemia cataract syndrome.
    Lachlan KL; Temple IK; Mumford AD
    Eur J Hum Genet; 2004 Oct; 12(10):790-6. PubMed ID: 15280904
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome.
    Luscieti S; Tolle G; Aranda J; Campos CB; Risse F; Morán É; Muckenthaler MU; Sánchez M
    Orphanet J Rare Dis; 2013 Feb; 8():30. PubMed ID: 23421845
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Brazilian family with hyperferritinemia-cataract syndrome: case report.
    Alvarenga AM; Silva NKD; Cançado RD; Carvalho LEMR; Santos PCJL
    Einstein (Sao Paulo); 2022; 20():eRC0076. PubMed ID: 36287435
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 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]  

  • 60. Hereditary hyperferritinaemia-cataract syndrome (HHCS) - an underestimated condition: ferritin light chain variant spectrum in German families.
    Volkmann M; Richter R; Herrmann T; Hentze S; Hör M; Hasche H; Selle B; Stremmel W; Gehrke SG
    Clin Chem Lab Med; 2019 Nov; 57(12):1837-1845. PubMed ID: 31211687
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.