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Journal Abstract Search

317 related items for PubMed ID: 15655144

  • 1. Prevalence of neurofibromatosis 1 in German children at elementary school enrollment.
    Lammert M, Friedman JM, Kluwe L, Mautner VF.
    Arch Dermatol; 2005 Jan; 141(1):71-4. PubMed ID: 15655144
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. [Neurofibromatosis in children. Our experience].
    López-Pisón J, Cuadrado-Martín M, Boldova-Aguar MC, Muñoz-Mellado A, Cabrerizo de Diago R, Peña-Segura JL.
    Rev Neurol; 2009 Aug; 37(9):820-5. PubMed ID: 14606048
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  • 4. [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 Aug; 20(5):393-400. PubMed ID: 18282435
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  • 5. Café-au-lait Macules and Neurofibromatosis Type 1: A Review of the Literature.
    Bernier A, Larbrisseau A, Perreault S.
    Pediatr Neurol; 2016 Jul; 60():24-29.e1. PubMed ID: 27212418
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  • 7. [Segmental neurofibromatosis in children. Presentation of 43 patients].
    Pascual-Castroviejo I, Pascual-Pascual SI, Velázquez-Fragua R, Viaño J, López-Gutiérrez JC.
    Rev Neurol; 2016 Jul; 47(8):399-403. PubMed ID: 18937200
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  • 8. 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
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  • 9. [Pheochromocytoma associated with neurofibromatosis 1: a report of two cases].
    Sano F, Fujikawa N, Hirai K, Ueki T, Kitami K.
    Hinyokika Kiyo; 2005 Dec; 51(12):793-5. PubMed ID: 16440725
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  • 10. [Neurofibromatosis].
    Wolkenstein P, Decq P.
    Neurochirurgie; 1998 Nov; 44(4):267-72. PubMed ID: 9864698
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  • 11. [Neurofibromatosis type 1: a survey of 195 patients].
    Overweg-Plandsoen WC, Weersink RG, Sillevis Smitt JH, Fleury P, van Asperen CJ.
    Ned Tijdschr Geneeskd; 1997 Mar 29; 141(13):624-9. PubMed ID: 9127578
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  • 12. Predicting neurofibromatosis type 1 risk among children with isolated café-au-lait macules.
    Ben-Shachar S, Dubov T, Toledano-Alhadef H, Mashiah J, Sprecher E, Constantini S, Leshno M, Messiaen LM.
    J Am Acad Dermatol; 2017 Jun 29; 76(6):1077-1083.e3. PubMed ID: 28318682
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  • 14. 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 29; 48(3):243-8. PubMed ID: 17914490
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  • 17. Epidemiology of neurofibromatosis type 1.
    Friedman JM.
    Am J Med Genet; 1999 Mar 26; 89(1):1-6. PubMed ID: 10469430
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  • 18. 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 26; 46(7):425-30. PubMed ID: 19366998
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  • 19. The nature and frequency of cognitive deficits in children with neurofibromatosis type 1.
    Hyman SL, Shores A, North KN.
    Neurology; 2005 Oct 11; 65(7):1037-44. PubMed ID: 16217056
    [Abstract] [Full Text] [Related]

  • 20. Early grade repetition and inattention associated with neurofibromatosis type 1.
    Coudé FX, Mignot C, Lyonnet S, Munnich A.
    J Atten Disord; 2007 Sep 11; 11(2):101-5. PubMed ID: 17494836
    [Abstract] [Full Text] [Related]

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