BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 17010267)

  • 1. Neurofibromatosis--review of the literature and case report.
    Pastar Z; Lipozencić J; Budimcić D; Tomljanović-Veselski M
    Acta Dermatovenerol Croat; 2006; 14(3):167-71. PubMed ID: 17010267
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial unilateral lentiginosis is mosaic neurofibromatosis type 1 or not?
    Yaşar Ş; Ersanli A; Göktay F; Aytekin S; Cebeci D; Güneş P
    J Dermatol; 2017 Jan; 44(1):29-35. PubMed ID: 27439996
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Head and neck manifestations of neurofibromatosis.
    Muecke M; Amedee RG
    J La State Med Soc; 1994 May; 146(5):183-6. PubMed ID: 8027629
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. Deep-seated segmental neurofibromatosis without café au lait spots.
    Ogose A; Hotta T; Imaizumi S; Saito H; Homma T; Takahashi HE
    Skeletal Radiol; 2000 Sep; 29(9):543-7. PubMed ID: 11000302
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial multiple cafe au lait spots.
    Arnsmeier SL; Riccardi VM; Paller AS
    Arch Dermatol; 1994 Nov; 130(11):1425-6. PubMed ID: 7979446
    [TBL] [Abstract][Full Text] [Related]  

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

  • 11. [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; 52(4):56-61. PubMed ID: 19354164
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype.
    Ruggieri M; Polizzi A; Salpietro V; Incorpora G; Nicita F; Pavone P; Falsaperla R; Nucifora C; Granata F; Distefano A; Padua L; Caltabiano R; Lanzafame S; Gabriele AL; Ortensi A; D'Orazi V; Panunzi A; Milone P; Mankad K; Platania N; Albanese V; Pavone V
    Neuropediatrics; 2013 Oct; 44(5):239-44. PubMed ID: 23780384
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Neurofibromatosis type 1 in childhood].
    Kongshaug N; Meyer B; Kolmannskog S
    Tidsskr Nor Laegeforen; 1999 Aug; 119(18):2653-7. PubMed ID: 10479978
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Neurofibromatosis].
    Wolkenstein P; Decq P
    Neurochirurgie; 1998 Nov; 44(4):267-72. PubMed ID: 9864698
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 36(3):197-203. PubMed ID: 10204844
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype.
    Pasmant E; Sabbagh A; Hanna N; Masliah-Planchon J; Jolly E; Goussard P; Ballerini P; Cartault F; Barbarot S; Landman-Parker J; Soufir N; Parfait B; Vidaud M; Wolkenstein P; Vidaud D; France RN
    J Med Genet; 2009 Jul; 46(7):425-30. PubMed ID: 19366998
    [TBL] [Abstract][Full Text] [Related]  

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

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

  • 19. Ophthalmological manifestations in segmental neurofibromatosis type 1.
    Ruggieri M; Pavone P; Polizzi A; Di Pietro M; Scuderi A; Gabriele A; Spalice A; Iannetti P
    Br J Ophthalmol; 2004 Nov; 88(11):1429-33. PubMed ID: 15489488
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features.
    Ruggieri M; Polizzi A; Spalice A; Salpietro V; Caltabiano R; D'Orazi V; Pavone P; Pirrone C; Magro G; Platania N; Cavallaro S; Muglia M; Nicita F
    Clin Genet; 2015 May; 87(5):401-10. PubMed ID: 25211147
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.