BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 12437553)

  • 21. Atrichia, ichthyosis, follicular hyperkeratosis, chronic candidiasis, keratitis, seizures, mental retardation and inguinal hernia: a severe manifestation of IFAP syndrome?
    Boente MC; Bibas-Bonet H; Coronel AM; Asial RA
    Eur J Dermatol; 2000 Mar; 10(2):98-102. PubMed ID: 10694306
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [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]  

  • 23. KID syndrome associated with features of ichthyosis hystrix.
    Nousari HC; Kimyai-Asadi A; Pinto JL
    Pediatr Dermatol; 2000; 17(2):115-7. PubMed ID: 10792799
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Porokeratotic eccrine duct and hair follicle nevus (PEHFN) associated with keratitis-ichthyosis-deafness (KID) syndrome.
    Criscione V; Lachiewicz A; Robinson-Bostom L; Grenier N; Dill SW
    Pediatr Dermatol; 2010; 27(5):514-7. PubMed ID: 21182641
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. [Successful topical cyclosporin A in the therapy of progressive vascularising keratitis in keratitis-ichthyosis-deafness (KID) syndrome (Senter syndrome)].
    Derse M; Wannke E; Payer H; Rohrbach JM; Zierhut M
    Klin Monbl Augenheilkd; 2002 May; 219(5):383-6. PubMed ID: 12094324
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome.
    Koppelhus U; Tranebjaerg L; Esberg G; Ramsing M; Lodahl M; Rendtorff ND; Olesen HV; Sommerlund M
    Clin Exp Dermatol; 2011 Mar; 36(2):142-8. PubMed ID: 20846357
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [A case for diagnosis: KID syndrome (keratosis, ichthyosis and deafness)].
    Stalder JF; Litoux P
    Ann Dermatol Venereol; 1988; 115(3):357-8. PubMed ID: 3408127
    [No Abstract]   [Full Text] [Related]  

  • 31. Keratitis, ichthyosis, and deafness (KID) syndrome: management with chronic oral ketoconazole therapy.
    Hazen PG; Walker AE; Stewart JJ; Carney JF; Engstrom CW; Turgeon KL
    Int J Dermatol; 1992 Jan; 31(1):58-9. PubMed ID: 1737693
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Do you know this syndrome?
    Enei ML; Cassettari A; Córdova S; Torres O; Paschoal F
    An Bras Dermatol; 2011; 86(4):819-21. PubMed ID: 21987161
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Ocular manifestations of keratitis-ichthyosis-deafness (KID) syndrome.
    Messmer EM; Kenyon KR; Rittinger O; Janecke AR; Kampik A
    Ophthalmology; 2005 Feb; 112(2):e1-6. PubMed ID: 15691545
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Malignant proliferating pilar tumors arising in KID syndrome: a report of two patients.
    Nyquist GG; Mumm C; Grau R; Crowson AN; Shurman DL; Benedetto P; Allen P; Lovelace K; Smith DW; Frieden I; Hybarger CP; Richard G
    Am J Med Genet A; 2007 Apr; 143A(7):734-41. PubMed ID: 17330861
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Phenotypic spectrum of autosomal recessive Keratitis-Ichthyosis-Deafness Syndrome (KIDAR) due to mutations in AP1B1.
    Faghihi F; Khamirani HJ; Zoghi S; Kamal N; Yeganeh BS; Dianatpour M; Bagher Tabei SM; Dastgheib SA
    Eur J Med Genet; 2022 Mar; 65(3):104449. PubMed ID: 35144013
    [TBL] [Abstract][Full Text] [Related]  

  • 37. KID Syndrome: report of a Scandinavian patient with connexin-26 gene mutation.
    Bygum A; Betz RC; Kragballe K; Steiniche T; Peeters N; Wuyts W; Nöthen MM
    Acta Derm Venereol; 2005; 85(2):152-5. PubMed ID: 15823911
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [KID syndrome: pathogenesis of ocular lesions].
    Tabet R; Smadja J; Hoang-Xuan T
    J Fr Ophtalmol; 2005 May; 28(5):521-6. PubMed ID: 15976720
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Histopathology and treatment of corneal disease in keratitis, ichthyosis, and deafness (KID) syndrome.
    Djalilian AR; Kim JY; Saeed HN; Holland EJ; Chan CC
    Eye (Lond); 2010 Apr; 24(4):738-40. PubMed ID: 19590522
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.