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Results: 1 to 20 of 153

Similar articles for PubMed (Select 1951425)

1.

Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndrome.

Wilson GN, Squires RH Jr, Weinberg AG.

Am J Med Genet. 1991 Sep 1;40(3):255-9.

PMID:
1951425
2.

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 Jan-Feb;51(1):35-43. Epub 2007 Oct 4.

PMID:
18024254
3.

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.

PMID:
2394858
4.

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.

PMID:
3232512
5.

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. Epub 2007 Mar 23. Review.

PMID:
17381453
6.

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. Epub 2002 Mar 22.

7.

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.

PMID:
19785089
8.

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 Sep-Oct;25(5):535-40. doi: 10.1111/j.1525-1470.2008.00767.x.

PMID:
18950394
9.

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. doi: 10.1097/MAO.0b013e3181cc09cd.

PMID:
20101161
10.

Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal form.

Sbidian E, Feldmann D, Bengoa J, Fraitag S, Abadie V, de Prost Y, Bodemer C, Hadj-Rabia S.

Clin Genet. 2010 Jun;77(6):587-92. doi: 10.1111/j.1399-0004.2009.01339.x. Epub 2010 Apr 14.

PMID:
20412116
11.

Auditory manifestations of Keratitis-Ichthyosis-Deafness (KID) syndrome.

Szymko-Bennett YM, Russell LJ, Bale SJ, Griffith AJ.

Laryngoscope. 2002 Feb;112(2):272-80.

PMID:
11889383
12.

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.

PMID:
3579358
13.

[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. German.

PMID:
12094324
14.

[Connexin 26 mutation and keratitis-ichthyosis-deafness (KID) syndrome].

Binder B, Hennies HC, Kraschl R, Smolle J.

J Dtsch Dermatol Ges. 2005 Feb;3(2):105-8. German.

PMID:
16351012
15.
16.

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.

PMID:
15691545
17.

Dandy-Walker malformation in patients with KID syndrome associated with a heterozygote mutation (p.Asp50Asn) in the GJB2 gene encoding connexin 26.

Todt I, Mazereeuw-Hautier J, Binder B, Willems PJ.

Clin Genet. 2009 Oct;76(4):404-8. doi: 10.1111/j.1399-0004.2009.01211.x.

PMID:
19793313
18.

Connexin 26 mutation in keratitis-ichthyosis-deafness (KID) syndrome in mother and daughter with combined conductive and sensorineural hearing loss.

Kelly B, Lozano A, Altenberg G, Makishima T.

Int J Dermatol. 2008 May;47(5):443-7. doi: 10.1111/j.1365-4632.2008.03603.x.

PMID:
18412859
19.

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. doi: 10.1111/j.1346-8138.2010.00839.x. No abstract available.

PMID:
20629838
20.

[Keratitis-ichthyosis-deafness (KID) syndrome].

Mazereeuw-Hautier J.

Ann Dermatol Venereol. 2008 Jan;135(1):80-2; quiz 79, 83. doi: 10.1016/j.annder.2007.11.013. Epub 2008 Jan 24. Review. French. No abstract available.

PMID:
18342082
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