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 *

126 related articles for article (PubMed ID: 10066965)

  • 1. A hyperkeratotic linear lesion in a girl with KID syndrome. A further example of early allelic loss?
    Restano L; Cambiaghi S; Brusasco A; Tardini G; Caputo R
    Eur J Dermatol; 1999 Mar; 9(2):142-3. PubMed ID: 10066965
    [No Abstract]   [Full Text] [Related]  

  • 2. The KID-syndrome in Finland. A report of four cases.
    Tuppurainen K; Fräki J; Karjalainen S; Paljärvi L; Suhonen R; Ryynänen M
    Acta Ophthalmol (Copenh); 1988 Dec; 66(6):692-8. PubMed ID: 3232512
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndrome.
    Wilson GN; Squires RH; Weinberg AG
    Am J Med Genet; 1991 Sep; 40(3):255-9. PubMed ID: 1951425
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas.
    Grob JJ; Breton A; Bonafe JL; Sauvan-Ferdani M; Bonerandi JJ
    Arch Dermatol; 1987 Jun; 123(6):777-82. PubMed ID: 3579358
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Atypical erythrokeratodermia with deafness, keratitis and double mycotic infection].
    Ginter G; Soyer HP
    Z Hautkr; 1988 Nov; 63(11):951-7. PubMed ID: 3239140
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Auditory manifestations of Keratitis-Ichthyosis-Deafness (KID) syndrome.
    Szymko-Bennett YM; Russell LJ; Bale SJ; Griffith AJ
    Laryngoscope; 2002 Feb; 112(2):272-80. PubMed ID: 11889383
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The pattern of inheritance in KID syndrome.
    Restano L; Cambiaghi S; Tadini G
    Pediatr Dermatol; 1999; 16(2):164-5. PubMed ID: 10337688
    [No Abstract]   [Full Text] [Related]  

  • 8. Surgical therapy in a patient with Keratosis-Ichthyosis-Deafness (KID) syndrome associated with follicular occlusion triad.
    Wenghoefer M; Allam JP; Novak N; Maintz L; Martini M; Bergé S
    Eur J Dermatol; 2007; 17(5):449-50. PubMed ID: 17673397
    [No Abstract]   [Full Text] [Related]  

  • 9. The keratitis, ichthyosis, and deafness (KID) syndrome.
    Skinner BA; Greist MC; Norins AL
    Arch Dermatol; 1981 May; 117(5):285-9. PubMed ID: 7224657
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Keratitis-ichthyosis-deafness (KID) syndrome].
    Mazereeuw-Hautier J
    Ann Dermatol Venereol; 2008 Jan; 135(1):80-2; quiz 79, 83. PubMed ID: 18342082
    [No Abstract]   [Full Text] [Related]  

  • 11. KID versus KED: What's in a name.
    Williams ML; McCalmont TH
    Pediatr Dermatol; 1996; 13(2):154-7. PubMed ID: 9122077
    [No Abstract]   [Full Text] [Related]  

  • 12. Familial occurrence of KID (keratitis, ichthyosis, deafness) syndrome. Case reports of a mother and daughter.
    Nazzaro V; Blanchet-Bardon C; Lorette G; Civatte J
    J Am Acad Dermatol; 1990 Aug; 23(2 Pt 2):385-8. PubMed ID: 2394858
    [TBL] [Abstract][Full Text] [Related]  

  • 13. KID syndrome: histopathological, immunohistochemical and molecular analysis of precancerous and cancerous skin lesions.
    Bergman R; Mercer A; Indelman M; Sprecher E; Haim N; Zoller L; Ben-Izhak O; Hershkovitz D
    Br J Dermatol; 2012 Feb; 166(2):455-7. PubMed ID: 21848689
    [No Abstract]   [Full Text] [Related]  

  • 14. [KID syndrome (keratitis-ichthyosis-deafness)].
    Puig L; Moreno A; Perez M; De Moragas JM
    Med Cutan Ibero Lat Am; 1987; 15(3):223-8. PubMed ID: 3312867
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Severe form of keratitis-ichthyosis-deafness (KID) syndrome associated with septic complications.
    Haruna K; Suga Y; Oizumi A; Mizuno Y; Endo H; Shimizu T; Hasegawa T; Ikeda S
    J Dermatol; 2010 Jul; 37(7):680-2. PubMed ID: 20629838
    [No Abstract]   [Full Text] [Related]  

  • 16. [Keratitis-ichthyosis-deafness (KID) syndrome: an observation in a child in sub-Saharan Africa].
    Barruet K; Saka B; Kombaté K; Mouhari-Toure A; Nguepmeni Noune J; Akakpo S; Tchangaï-Walla K; Pitché P
    Ann Dermatol Venereol; 2011 May; 138(5):453-5. PubMed ID: 21570577
    [No Abstract]   [Full Text] [Related]  

  • 17. A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome.
    van Steensel MA; van Geel M; Nahuys M; Smitt JH; Steijlen PM
    J Invest Dermatol; 2002 Apr; 118(4):724-7. PubMed ID: 11918723
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Keratitis-Ichthyosis-Deafness Syndrome: Early Death Caused by the GJB2 Mutation p.Gly12Arg.
    Godillot C; Severino-Freire M; Michaud V; Boralevi F; Labrèze C; Guigonis V; Onnis G; Morice-Picard F; Mazereeuw-Hautier J
    Acta Derm Venereol; 2019 Sep; 99(10):921-922. PubMed ID: 31099403
    [No Abstract]   [Full Text] [Related]  

  • 19. [A rare oculo-auriculo-cutaneous syndrome (Burns' syndrome)].
    Legrand J; Litoux P; Quere M; Stalder JF; Ertus M
    J Fr Ophtalmol; 1982; 5(6-7):441-5. PubMed ID: 7130633
    [No Abstract]   [Full Text] [Related]  

  • 20. [Diagnostics of keratitis-ichthyosis-deafness syndrome (KID- syndrome)].
    Markova TG; Brazhkina NB; Bliznets EV; Poliakov AV; Tavartkiladze GA
    Vestn Otorinolaringol; 2012; (3):58-61. PubMed ID: 22951689
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.