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

295 related items for PubMed ID: 24519776

  • 1. [Neurofibromatosis type 1 - description of clinical features and molecular mechanism of the disease].
    Bikowska-Opalach B, Jackowska T.
    Med Wieku Rozwoj; 2013; 17(4):334-40. PubMed ID: 24519776
    [Abstract] [Full Text] [Related]

  • 2. [Neurofibromatosis type 1 (von Recklinghausen's disease or peripheral neurofibromatosis): from phenotype to gene].
    Sabol Z, Kipke-Sabol L.
    Lijec Vjesn; 2005; 127(11-12):303-11. PubMed ID: 16583938
    [Abstract] [Full Text] [Related]

  • 3. [Developmental manifestation in children with neurofibromatosis type 1].
    Cohen R, Shuper A.
    Harefuah; 2010 Jan; 149(1):49-52, 61. PubMed ID: 20422842
    [Abstract] [Full Text] [Related]

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

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. [Neurofibromatosis--an inborn genetic disorder with susceptibility to neoplasia].
    Karwacki MW, Woźniak W.
    Med Wieku Rozwoj; 2006 Jan; 10(3 Pt 2):923-48. PubMed ID: 17401183
    [Abstract] [Full Text] [Related]

  • 9. [Unusual clinical manifestations of type 1 neurofibromatosis].
    Komlósi K, Polgár N, Hadzsiev K, Ottóffy G, Illés T, Dóczi T, Melegh B.
    Orv Hetil; 2011 Dec 04; 152(49):1965-70. PubMed ID: 22106164
    [Abstract] [Full Text] [Related]

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

  • 11. Lisch nodules: a diagnostic sign for Von Recklinghausen's neurofibromatosis.
    Norman RA.
    J Am Optom Assoc; 1983 Jun 04; 54(6):533-5. PubMed ID: 6409954
    [Abstract] [Full Text] [Related]

  • 12. Genetic and clinical considerations in six cases with neurofibromatosis type 1.
    Buteică E, Stoicescu I, Burada F, Stănoiu B.
    Rom J Morphol Embryol; 2007 Jun 04; 48(3):243-8. PubMed ID: 17914490
    [Abstract] [Full Text] [Related]

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

  • 14. Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene.
    Colman SD, Williams CA, Wallace MR.
    Nat Genet; 1995 Sep 04; 11(1):90-2. PubMed ID: 7550323
    [Abstract] [Full Text] [Related]

  • 15. Neurofibromin in neurofibromatosis type 1 - mutations in NF1gene as a cause of disease.
    Abramowicz A, Gos M.
    Dev Period Med; 2014 Sep 04; 18(3):297-306. PubMed ID: 25182393
    [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. NF1 frameshift mutation (c.6520_6523delGAGA) association with nervous system tumors and bone abnormalities in a Chinese patient with neurofibromatosis type 1.
    Su SY, Zhou X, Pang XM, Chen CY, Li SH, Liu JL.
    Genet Mol Res; 2016 Apr 07; 15(2):. PubMed ID: 27173220
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.