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Journal Abstract Search

782 related items for PubMed ID: 18282435

  • 1. [Managing children with neurofibromatosis type 1: what should we look for?].
    Martins CL, Monteiro JP, Farias A, Fernandes R, Fonseca MJ.
    Acta Med Port; 2007; 20(5):393-400. PubMed ID: 18282435
    [Abstract] [Full Text] [Related]

  • 2. Neurological complications involving the central nervous system in neurofibromatosis type 1.
    Hsieh HY, Wu T, Wang CJ, Chin SC, Chen YR.
    Acta Neurol Taiwan; 2007 Jun; 16(2):68-73. PubMed ID: 17685129
    [Abstract] [Full Text] [Related]

  • 3. [Neurofibromatosis type 1 (von Recklinghausen's disease or peripheral neurofibromatosis): from phenotype to gene].
    Sabol Z, Kipke-Sabol L.
    Lijec Vjesn; 2005 Jun; 127(11-12):303-11. PubMed ID: 16583938
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  • 10. Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling.
    Terzi YK, Oguzkan-Balci S, Anlar B, Aysun S, Guran S, Ayter S.
    Genet Couns; 2009 Jun; 20(2):195-202. PubMed ID: 19650418
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  • 11. Predictive value of café au lait macules at initial consultation in the diagnosis of neurofibromatosis type 1.
    Nunley KS, Gao F, Albers AC, Bayliss SJ, Gutmann DH.
    Arch Dermatol; 2009 Aug; 145(8):883-7. PubMed ID: 19687418
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  • 12. [From gene to disease; neurofibromatosis type 1].
    de Goede-Bolder A, Cnossen MH, Dooijes D, van den Ouweland AM, Niermeijer MF.
    Ned Tijdschr Geneeskd; 2001 Sep 08; 145(36):1736-8. PubMed ID: 11572174
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  • 13. [Neurofibromatosis type 1 in childhood].
    Kongshaug N, Meyer B, Kolmannskog S.
    Tidsskr Nor Laegeforen; 1999 Aug 10; 119(18):2653-7. PubMed ID: 10479978
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  • 14. Learning disabilities in children with neurofibromatosis type 1: subtypes, cognitive profile, and attention-deficit-hyperactivity disorder.
    Hyman SL, Arthur Shores E, North KN.
    Dev Med Child Neurol; 2006 Dec 10; 48(12):973-7. PubMed ID: 17109785
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  • 15. A clinical study of type 1 neurofibromatosis in north west England.
    McGaughran JM, Harris DI, Donnai D, Teare D, MacLeod R, Westerbeek R, Kingston H, Super M, Harris R, Evans DG.
    J Med Genet; 1999 Mar 10; 36(3):197-203. PubMed ID: 10204844
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  • 16. Eye disorders in neurofibromatosis (NF1).
    Kordić R, Sabol Z, Cerovski B, Katusić D, Jukić T.
    Coll Antropol; 2005 Mar 10; 29 Suppl 1():29-31. PubMed ID: 16193672
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  • 17. Unusual clustering of brain tumours in a family with NF1 and variable expression of cutaneous features.
    Faravelli F, Upadhyaya M, Osborn M, Huson SM, Hayward R, Winter R.
    J Med Genet; 1999 Dec 10; 36(12):893-6. PubMed ID: 10593996
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  • 18. Atypical hematologic and renal manifestations in neurofibromatosis type I: coincidence or pathophysiological link?
    Van-Gils J, Harambat J, Jubert C, Vidaud D, Llanas B, Perel Y, Lacombe D, Goizet C.
    Eur J Med Genet; 2014 Dec 10; 57(11-12):639-42. PubMed ID: 25234363
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  • 19. Diagnostic outcome in children with multiple café au lait spots.
    Korf BR.
    Pediatrics; 1992 Dec 10; 90(6):924-7. PubMed ID: 1344978
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  • 20. Analysis of intrafamilial phenotypic variation in neurofibromatosis 1 (NF1).
    Szudek J, Joe H, Friedman JM.
    Genet Epidemiol; 2002 Aug 10; 23(2):150-64. PubMed ID: 12214308
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