BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 25758847)

  • 1. Oral squamous cell carcinoma in a patient with keratitis-ichthyosis-deafness syndrome: a rare case.
    Homeida L; Wiley RT; Fatahzadeh M
    Oral Surg Oral Med Oral Pathol Oral Radiol; 2015 Apr; 119(4):e226-32. PubMed ID: 25758847
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Connexin 26 (GJB2) mutations in keratitis-ichthyosis-deafness syndrome presenting with squamous cell carcinoma.
    Sakabe J; Yoshiki R; Sugita K; Haruyama S; Sawada Y; Kabashima R; Bito T; Nakamura M; Tokura Y
    J Dermatol; 2012 Sep; 39(9):814-5. PubMed ID: 22098592
    [No Abstract]   [Full Text] [Related]  

  • 3. Squamous cell carcinoma arising from Keratitis-ichthyosis-deafness syndrome.
    Mayama H; Fujimura T; Asano M; Kambayashi Y; Numata Y; Aiba S
    Acta Derm Venereol; 2013 Sep; 93(5):583-4. PubMed ID: 23388822
    [No Abstract]   [Full Text] [Related]  

  • 4. Keratitis, ichthyosis, and deafness syndrome: a review of infectious and neoplastic complications.
    Coggshall K; Farsani T; Ruben B; McCalmont TH; Berger TG; Fox LP; Shinkai K
    J Am Acad Dermatol; 2013 Jul; 69(1):127-34. PubMed ID: 23384797
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome.
    Griffith AJ; Yang Y; Pryor SP; Park HJ; Jabs EW; Nadol JB; Russell LJ; Wasserman DI; Richard G; Adams JC; Merchant SN
    Laryngoscope; 2006 Aug; 116(8):1404-8. PubMed ID: 16885744
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A rare connexin 26 mutation in a patient with a forme fruste of keratitis-ichthyosis-deafness (KID) syndrome.
    Neoh CY; Chen H; Ng SK; Lane EB; Common JE
    Int J Dermatol; 2009 Oct; 48(10):1078-81. PubMed ID: 19785089
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Squamous cell carcinoma in congenital ichthyosis with deafness and keratitis. A case report and review of the literature.
    Madariaga J; Fromowitz F; Phillips M; Hoover HC
    Cancer; 1986 May; 57(10):2026-9. PubMed ID: 3955509
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E.
    Jonard L; Feldmann D; Parsy C; Freitag S; Sinico M; Koval C; Grati M; Couderc R; Denoyelle F; Bodemer C; Marlin S; Hadj-Rabia S
    Eur J Med Genet; 2008; 51(1):35-43. PubMed ID: 18024254
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cochlear implantation in children with keratitis-ichthyosis-deafness (KID) syndrome: outcomes in three cases.
    Barker EJ; Briggs RJ
    Cochlear Implants Int; 2009 Sep; 10(3):166-73. PubMed ID: 19023871
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel dominant and a de novo mutation in the GJB2 gene (connexin-26) cause keratitis-ichthyosis-deafness syndrome: implication for cochlear implantation.
    Arndt S; Aschendorff A; Schild C; Beck R; Maier W; Laszig R; Birkenhäger R
    Otol Neurotol; 2010 Feb; 31(2):210-5. PubMed ID: 20101161
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Extending the phenotypic spectrum of keratitis-ichthyosis-deafness syndrome: report of a patient with GJB2 (G12R) Connexin 26 mutation and unusual clinical findings.
    Lazic T; Li Q; Frank M; Uitto J; Zhou LH
    Pediatr Dermatol; 2012; 29(3):349-57. PubMed ID: 22011219
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Keratitis, ichthyosis, and deafness (KID) syndrome with cerebellar hypoplasia.
    Hsu HC; Lin GS; Li WM
    Int J Dermatol; 1988 Dec; 27(10):695-7. PubMed ID: 3235255
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Systemic cytomegalovirus in a patient with the keratitis, ichthyosis, and deafness (KID) syndrome.
    Helm K; Lane AT; Orosz J; Metlay L
    Pediatr Dermatol; 1990 Mar; 7(1):54-6. PubMed ID: 2160657
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome.
    Richard G; Rouan F; Willoughby CE; Brown N; Chung P; Ryynänen M; Jabs EW; Bale SJ; DiGiovanna JJ; Uitto J; Russell L
    Am J Hum Genet; 2002 May; 70(5):1341-8. PubMed ID: 11912510
    [TBL] [Abstract][Full Text] [Related]  

  • 16. KID syndrome (keratitis, ichthyosis, and deafness) and chronic mucocutaneous candidiasis: case report and review of the literature.
    Harms M; Gilardi S; Levy PM; Saurat JH
    Pediatr Dermatol; 1984 Jul; 2(1):1-7. PubMed ID: 6390393
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Keratitis, ichthyosis and deafness (KID syndrome).
    Singh K
    Australas J Dermatol; 1987 Apr; 28(1):38-41. PubMed ID: 3426484
    [No Abstract]   [Full Text] [Related]  

  • 18. Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome.
    Kaku Y; Tanizaki H; Tanioka M; Sakabe J; Miyagawa-Hayashino A; Tokura Y; Miyachi Y; Kabashima K
    Br J Dermatol; 2012 Jan; 166(1):222-4. PubMed ID: 21777204
    [No Abstract]   [Full Text] [Related]  

  • 19. A report of GJB2 (N14K) Connexin 26 mutation in two patients--a new subtype of KID syndrome?
    Lazic T; Horii KA; Richard G; Wasserman DI; Antaya RJ
    Pediatr Dermatol; 2008; 25(5):535-40. PubMed ID: 18950394
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.