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Journal Abstract Search

631 related items for PubMed ID: 11385791

  • 1. [Syndromes 18. Von Recklinghausen's disease].
    Baart JA, van Hagen JM.
    Ned Tijdschr Tandheelkd; 2000 Feb; 107(2):57-9. PubMed ID: 11385791
    [Abstract] [Full Text] [Related]

  • 2. Giant café-au-lait macule in neurofibromatosis 1: a type 2 segmental manifestation of neurofibromatosis 1?
    Yang CC, Happle R, Chao SC, Yu-Yun Lee J, Chen W.
    J Am Acad Dermatol; 2008 Mar; 58(3):493-7. PubMed ID: 18280349
    [Abstract] [Full Text] [Related]

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

  • 4. [Lisch nodules. Markers for a non-invasive diagnosis in Recklinghausen neurofibromatosis].
    Crişan M, Talu S, Florea M, Coprean D, Cosgarea R, Crişan D.
    Oftalmologia; 2008 Jun; 52(4):56-61. PubMed ID: 19354164
    [Abstract] [Full Text] [Related]

  • 5. Autoimmune haemolysis as an unusual cause of anaemia in von Recklinghausen's disease.
    Tekin F, Ozutemiz O, Carcurgan S, Ilter T.
    Neth J Med; 2004 Oct; 62(9):337-9. PubMed ID: 15635820
    [Abstract] [Full Text] [Related]

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

  • 7. Clinical and genetic significance of unilateral Lisch nodules.
    Ceuterick SD, Van Den Ende JJ, Smets RM.
    Bull Soc Belge Ophtalmol; 2005 Oct; (295):49-53. PubMed ID: 15849989
    [Abstract] [Full Text] [Related]

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

  • 9. [Neurofibromatosis type 1 and hypertension in pediatrics: case report].
    Demarchi I, Genoni G, Prodam F, Petri A, Busti A, Cortese L, Negro M, Bellone S, Acucella G, Bona G.
    Minerva Pediatr; 2011 Aug; 63(4):335-9. PubMed ID: 21909069
    [Abstract] [Full Text] [Related]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. Plexiform neurofibroma of the tongue: a case report of a child.
    Güneri EA, Akoğlu E, Sütay S, Ceryan K, Sağol O, Pabuçcuoğlu U.
    Turk J Pediatr; 2006 Sep 08; 48(2):155-8. PubMed ID: 16848118
    [Abstract] [Full Text] [Related]

  • 12. [Developmental manifestation in children with neurofibromatosis type 1].
    Cohen R, Shuper A.
    Harefuah; 2010 Jan 08; 149(1):49-52, 61. PubMed ID: 20422842
    [Abstract] [Full Text] [Related]

  • 13. A child with axillary freckling and café au lait spots.
    Wainer S.
    CMAJ; 2002 Aug 06; 167(3):282-3. PubMed ID: 12186179
    [No Abstract] [Full Text] [Related]

  • 14. [Lisch nodule in neurofibromatosis type 1].
    Abaloun Y, Ajhoun Y.
    Pan Afr Med J; 2017 Aug 06; 27():218. PubMed ID: 28979620
    [Abstract] [Full Text] [Related]

  • 15. Vitamin D3 analogues improve café au lait spots in patients with von Recklinghausen's disease: experimental and clinical studies.
    Nakayama J, Kiryu H, Urabe K, Matsuo S, Shibata S, Koga T, Furue M.
    Eur J Dermatol; 1999 Aug 06; 9(3):202-6. PubMed ID: 10210785
    [Abstract] [Full Text] [Related]

  • 16. Eye disorders in neurofibromatosis (NF1).
    Kordić R, Sabol Z, Cerovski B, Katusić D, Jukić T.
    Coll Antropol; 2005 Aug 06; 29 Suppl 1():29-31. PubMed ID: 16193672
    [Abstract] [Full Text] [Related]

  • 17. Analysis of intrafamilial phenotypic variation in neurofibromatosis 1 (NF1).
    Szudek J, Joe H, Friedman JM.
    Genet Epidemiol; 2002 Aug 06; 23(2):150-64. PubMed ID: 12214308
    [Abstract] [Full Text] [Related]

  • 18. 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 Aug 06; 20(2):195-202. PubMed ID: 19650418
    [Abstract] [Full Text] [Related]

  • 19. Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene.
    Colman SD, Williams CA, Wallace MR.
    Nat Genet; 1995 Sep 06; 11(1):90-2. PubMed ID: 7550323
    [Abstract] [Full Text] [Related]

  • 20. Diagnostic outcome in children with multiple café au lait spots.
    Korf BR.
    Pediatrics; 1992 Dec 06; 90(6):924-7. PubMed ID: 1344978
    [Abstract] [Full Text] [Related]

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