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 *

131 related articles for article (PubMed ID: 32367610)

  • 21. Keratitis, ichthyosis, and deafness (KID syndrome): review of the literature and proposal of a new terminology.
    Caceres-Rios H; Tamayo-Sanchez L; Duran-Mckinster C; de la Luz Orozco M; Ruiz-Maldonado R
    Pediatr Dermatol; 1996; 13(2):105-13. PubMed ID: 9122065
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. KID syndrome.
    Abdollahi A; Hallaji Z; Esmaili N; Valikhani M; Barzegari M; Akhyani M; Toosi S; Miresmaili A
    Dermatol Online J; 2007 Oct; 13(4):11. PubMed ID: 18319008
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. What syndrome is this? KID syndrome (keratitis, ichthyosis, deafness).
    Lenane P; Cammisuli S; Chitayat D; Krafchik B
    Pediatr Dermatol; 2006; 23(1):81-3. PubMed ID: 16445421
    [No Abstract]   [Full Text] [Related]  

  • 26. Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients.
    Mazereeuw-Hautier J; Bitoun E; Chevrant-Breton J; Man SY; Bodemer C; Prins C; Antille C; Saurat JH; Atherton D; Harper JI; Kelsell DP; Hovnanian A
    Br J Dermatol; 2007 May; 156(5):1015-9. PubMed ID: 17381453
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [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]  

  • 28. 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]  

  • 29. Inherited ichthyosis and fungal infection: an update on pathogenesis and treatment strategies.
    Miao H; Dong R; Zhang S; Yang L; Liu Y; Wang T
    J Dtsch Dermatol Ges; 2021 Mar; 19(3):341-350. PubMed ID: 33448147
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Antenatal Findings of Keratitis-Ichthyosis-Deafness Syndrome.
    Okmen F; Hortu I; Jafarova U; Imamoglu M; Ekici H; Ergenoglu AM
    J Obstet Gynaecol Can; 2020 Apr; 42(4):504-506. PubMed ID: 31421982
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. Clinical and electrophysiological studies in a patient with keratitis, ichthyosis and deafness (KID) syndrome.
    Chia LG; Li WM
    J Neurogenet; 1987 Jan; 4(1):57-64. PubMed ID: 3559795
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Trichothiodystrophy-like hair abnormalities in a child with keratitis ichthyosis deafness syndrome.
    De Raeve L; Bonduelle M; Deconinck H; Roseeuw D; Stene JJ
    Pediatr Dermatol; 2008; 25(4):466-9. PubMed ID: 18789090
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. Diffuse hyperkeratosis in a deaf and blind 48-year-old woman--quiz case. Diagnosis: keratitis-ichthyosis-deafness (KID) syndrome with secondary dermatophytosis.
    Machan M; Kestenbaum T; Fraga GR
    Arch Dermatol; 2012 Oct; 148(10):1199-200. PubMed ID: 23069961
    [No Abstract]   [Full Text] [Related]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 7.