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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 2511319)

  • 1. A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.
    Huson SM; Compston DA; Harper PS
    J Med Genet; 1989 Nov; 26(11):712-21. PubMed ID: 2511319
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Von Recklinghausen neurofibromatosis. A clinical and population study in south-east Wales.
    Huson SM; Harper PS; Compston DA
    Brain; 1988 Dec; 111 ( Pt 6)():1355-81. PubMed ID: 3145091
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Neurofibromatosis--an inborn genetic disorder with susceptibility to neoplasia].
    Karwacki MW; Woźniak W
    Med Wieku Rozwoj; 2006; 10(3 Pt 2):923-48. PubMed ID: 17401183
    [TBL] [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; 52(4):56-61. PubMed ID: 19354164
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.
    Charrow J; Listernick R; Ward K
    Am J Med Genet; 1993 Mar; 45(5):606-8. PubMed ID: 8456833
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity.
    Huson SM; Compston DA; Clark P; Harper PS
    J Med Genet; 1989 Nov; 26(11):704-11. PubMed ID: 2511318
    [TBL] [Abstract][Full Text] [Related]  

  • 7. High frequencies of plexiform neurofibromas, mental retardation, learning difficulties, and scoliosis in Brazilian patients with neurofibromatosis type 1.
    Trovó-Marqui AB; Goloni-Bertollo EM; Valério NI; Pavarino-Bertelli EC; Muniz MP; Teixeira MF; Antonio JR; Tajara EH
    Braz J Med Biol Res; 2005 Sep; 38(9):1441-7. PubMed ID: 16138229
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 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. Neurofibromatosis.
    Wander JV; Das Gupta TK
    Curr Probl Surg; 1977 Feb; 14(2):1-81. PubMed ID: 405178
    [No Abstract]   [Full Text] [Related]  

  • 11. Bone abnormalities occurring in the follow-up of the patients with neurofibromatosis type 1.
    Georgescu EF; Stănescu L; Georgescu AC; Dumitrescu D; Foarfă C; Călin G
    Rom J Morphol Embryol; 2007; 48(3):249-56. PubMed ID: 17914491
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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; 152(49):1965-70. PubMed ID: 22106164
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pathophysiology of neurofibromatosis. IV. Dermatologic insights into heterogeneity and pathogenesis.
    Riccardi VM
    J Am Acad Dermatol; 1980 Aug; 3(2):157-66. PubMed ID: 6774000
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients.
    Ars E; Kruyer H; Morell M; Pros E; Serra E; Ravella A; Estivill X; Lázaro C
    J Med Genet; 2003 Jun; 40(6):e82. PubMed ID: 12807981
    [No Abstract]   [Full Text] [Related]  

  • 16. Relationship between café-au-lait spots as the only symptom and peripheral neurofibromatosis (NF1): a follow-up study.
    Fois A; Calistri L; Balestri P; Vivarelli R; Bartalini G; Mancini L; Berardi A; Vanni M
    Eur J Pediatr; 1993 Jun; 152(6):500-4. PubMed ID: 8335018
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Von Recklinghausen neurofibromatosis. Incidence of iris hamartomata.
    Lewis RA; Riccardi VM
    Ophthalmology; 1981 Apr; 88(4):348-54. PubMed ID: 6789269
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Thoracic findings in neurofibromatosis].
    Camsari G; Gür A; Ozkan G; Bakan ND; Zengin F; Külcü A
    Tuberk Toraks; 2006; 54(3):267-72. PubMed ID: 17001545
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neurofibromatosis in childhood: a review of 25 cases.
    Pollnitz R
    Med J Aust; 1976 Jul; 2(2):49-52. PubMed ID: 824536
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.