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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

187 related items for PubMed ID: 9378401

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. 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 15; 90(2):814-21. PubMed ID: 9226182
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. 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 15; 61(9):291-5. PubMed ID: 14692443
    [Abstract] [Full Text] [Related]

  • 6. Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract.
    Beaumont C, Leneuve P, Devaux I, Scoazec JY, Berthier M, Loiseau MN, Grandchamp B, Bonneau D.
    Nat Genet; 1995 Dec 15; 11(4):444-6. PubMed ID: 7493028
    [Abstract] [Full Text] [Related]

  • 7. A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract.
    Girelli D, Olivieri O, De Franceschi L, Corrocher R, Bergamaschi G, Cazzola M.
    Br J Haematol; 1995 Aug 15; 90(4):931-4. PubMed ID: 7669675
    [Abstract] [Full Text] [Related]

  • 8. 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 Aug 15; 36(1):33-40. PubMed ID: 16406710
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. [Hereditary hyperferritinaemia-cataract syndrome].
    van der Klooster JM.
    Ned Tijdschr Geneeskd; 2003 Sep 27; 147(39):1923-8. PubMed ID: 14560693
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Dual diagnoses of hereditary hyperferritinaemia-cataract syndrome and hereditary haemochromatosis.
    Hughes M, Vosylius P.
    Clin Lab Haematol; 2006 Oct 27; 28(5):357-9. PubMed ID: 16999731
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [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 10; 127(2):55-8. PubMed ID: 16900584
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.