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 *

345 related articles for article (PubMed ID: 12214308)

  • 41. [Unilateral lentiginosis--a segmental neurofibromatosis without neurofibromas].
    Gerhards G; Hamm H
    Hautarzt; 1992 Aug; 43(8):491-5. PubMed ID: 1506215
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Café-au-lait spots in neurofibromatosis type 1 and in healthy control individuals: hyperpigmentation of a different kind?
    De Schepper S; Boucneau J; Vander Haeghen Y; Messiaen L; Naeyaert JM; Lambert J
    Arch Dermatol Res; 2006 Apr; 297(10):439-49. PubMed ID: 16479403
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Clinical features of 58 Japanese patients with mosaic neurofibromatosis 1.
    Tanito K; Ota A; Kamide R; Nakagawa H; Niimura M
    J Dermatol; 2014 Aug; 41(8):724-8. PubMed ID: 25041723
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Bilateral segmental neurofibromatosis: a case report and review.
    Gonzalez G; Russi ME; Lodeiros A
    Pediatr Neurol; 2007 Jan; 36(1):51-3. PubMed ID: 17162198
    [TBL] [Abstract][Full Text] [Related]  

  • 45. An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots and Freckling. Part II. Other Skin Manifestations Characteristic of NF1. NF1 and Cancer.
    Hernández-Martín A; Duat-Rodríguez A
    Actas Dermosifiliogr; 2016; 107(6):465-73. PubMed ID: 26956402
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas.
    Pinna V; Lanari V; Daniele P; Consoli F; Agolini E; Margiotti K; Bottillo I; Torrente I; Bruselles A; Fusilli C; Ficcadenti A; Bargiacchi S; Trevisson E; Forzan M; Giustini S; Leoni C; Zampino G; Digilio MC; Dallapiccola B; Clementi M; Tartaglia M; De Luca A
    Eur J Hum Genet; 2015 Aug; 23(8):1068-71. PubMed ID: 25370043
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Multiple spinal ganglioneuromas in a patient harboring a pathogenic NF1 mutation.
    Bacci C; Sestini R; Ammannati F; Bianchini E; Palladino T; Carella M; Melchionda S; Zelante L; Papi L
    Clin Genet; 2010 Mar; 77(3):293-7. PubMed ID: 19863548
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Bilateral segmental neurofibromatosis with gastric carcinoma.
    Kajimoto A; Oiso N; Fukai K; Ishii M
    Clin Exp Dermatol; 2007 Jan; 32(1):43-4. PubMed ID: 16939586
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Neurofibromatosis. A clinical and genetic study of 96 cases in Gothenburg, Sweden.
    Samuelsson B; Axelsson R
    Acta Derm Venereol Suppl (Stockh); 1981; 95():67-71. PubMed ID: 6807042
    [TBL] [Abstract][Full Text] [Related]  

  • 53. An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots, Freckling, and Neurofibromas. An Update. Part I. Dermatological Clinical Criteria Diagnostic of the Disease.
    Hernández-Martín A; Duat-Rodríguez A
    Actas Dermosifiliogr; 2016; 107(6):454-64. PubMed ID: 26979265
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A severe form of Noonan syndrome and autosomal dominant café-au-lait spots - evidence for different genetic origins.
    Nyström AM; Ekvall S; Strömberg B; Holmström G; Thuresson AC; Annerén G; Bondeson ML
    Acta Paediatr; 2009 Apr; 98(4):693-8. PubMed ID: 19120036
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [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; 2003 Nov 1-15; 37(9):820-5. PubMed ID: 14606048
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Is the distribution of dermal neurofibromas in neurofibromatosis type 1 (NF1) related to the pattern of the skin surface temperature?
    Kaufmann D; Tinschert S; Algermissen B
    Eur J Dermatol; 2001; 11(6):521-6. PubMed ID: 11701400
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [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]  

  • 59. Clinicopathological study of neurofibromatosis type 1: an experience in Nigeria.
    Odebode TO; Afolayan EA; Adigun IA; Daramola OO
    Int J Dermatol; 2005 Feb; 44(2):116-20. PubMed ID: 15689208
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1.
    Gabriele AL; Ruggieri M; Patitucci A; Magariello A; Conforti FL; Mazzei R; Muglia M; Ungaro C; Di Palma G; Citrigno L; Sproviero W; Gambardella A; Quattrone A
    Childs Nerv Syst; 2011 Apr; 27(4):635-8. PubMed ID: 20927530
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.