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.
70. A case of keratitis ichthyosis deafness (KID) syndrome associated with Dandy-Walker. Zhang XB; Li CX J Eur Acad Dermatol Venereol; 2007 May; 21(5):706-7. PubMed ID: 17448003 [No Abstract] [Full Text] [Related]
71. Connexin hemichannel inhibition ameliorates epidermal pathology in a mouse model of keratitis ichthyosis deafness syndrome. Sellitto C; Li L; White TW Sci Rep; 2021 Dec; 11(1):24118. PubMed ID: 34916582 [TBL] [Abstract][Full Text] [Related]
72. Connexin mutations causing skin disease and deafness increase hemichannel activity and cell death when expressed in Xenopus oocytes. Lee JR; Derosa AM; White TW J Invest Dermatol; 2009 Apr; 129(4):870-8. PubMed ID: 18987669 [TBL] [Abstract][Full Text] [Related]
73. 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]
74. A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad. Montgomery JR; White TW; Martin BL; Turner ML; Holland SM J Am Acad Dermatol; 2004 Sep; 51(3):377-82. PubMed ID: 15337980 [TBL] [Abstract][Full Text] [Related]
75. De novo mutation in the gene encoding connexin-26 (GJB2) in a sporadic case of keratitis-ichthyosis-deafness (KID) syndrome. Alvarez A; del Castillo I; Pera A; Villamar M; Moreno-Pelayo MA; Moreno F; Moreno R; Tapia MC Am J Med Genet A; 2003 Feb; 117A(1):89-91. PubMed ID: 12548749 [No Abstract] [Full Text] [Related]
76. Conserved glycine at position 45 of major cochlear connexins constitutes a vital component of the Ca²⁺ sensor for gating of gap junction hemichannels. Zhang Y; Hao H Biochem Biophys Res Commun; 2013 Jul; 436(3):424-9. PubMed ID: 23756814 [TBL] [Abstract][Full Text] [Related]
77. Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability in clinical expression from mutations of R75W and R75Q in the GJB2 gene. Birkenhäger R; Lüblinghoff N; Prera E; Schild C; Aschendorff A; Arndt S Am J Med Genet A; 2010 Jul; 152A(7):1798-802. PubMed ID: 20583176 [TBL] [Abstract][Full Text] [Related]
78. 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]
79. Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes' clinical diagnostics. Kutkowska-Kaźmierczak A; Niepokój K; Wertheim-Tysarowska K; Giza A; Mordasewicz-Goliszewska M; Bal J; Obersztyn E J Appl Genet; 2015 Aug; 56(3):329-37. PubMed ID: 25575739 [TBL] [Abstract][Full Text] [Related]
80. 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] [Previous] [Next] [New Search]