PubMed

Usher syndrome in the city of Birmingham--prevalence and clinical classification.

Hope CI, Bundey S, Proops D, Fielder AR.

Br J Ophthalmol. 1997 Jan;81(1):46-53.PMID: 9135408 [PubMed - indexed for MEDLINE]Related articlesFree article

Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway.

Grøndahl J.

Clin Genet. 1987 Apr;31(4):255-64.PMID: 3594933 [PubMed - indexed for MEDLINE]Related articles

Clinical and genetic linkage analysis of a large Venezuelan kindred with Usher syndrome.

Keogh IJ, Godinho RN, Wu TP, Diaz de Palacios AM, Palacios N, Bello de Alford M, De Almada MI, MarPalacios N, Vazquez A, Mattei R, Seidman C, Seidman J, Eavey RD.

Int J Pediatr Otorhinolaryngol. 2004 Aug;68(8):1063-8.PMID: 15236894 [PubMed - indexed for MEDLINE]Related articles

Prevalence and geographical distribution of Usher syndrome in Germany.

Spandau UH, Rohrschneider K.

Graefes Arch Clin Exp Ophthalmol. 2002 Jun;240(6):495-8. Epub 2002 May 23.PMID: 12107518 [PubMed - indexed for MEDLINE]Related articles

Prevalence of retinitis pigmentosa in Maine.

Bunker CH, Berson EL, Bromley WC, Hayes RP, Roderick TH.

Am J Ophthalmol. 1984 Mar;97(3):357-65.PMID: 6702974 [PubMed - indexed for MEDLINE]Related articles

[From gene to disease; genetic causes of hearing loss and visual impairment sometimes accompanied by vestibular problems (Usher syndrome)]

Pennings RJ, Kremer H, Deutman AF, Kimberling WJ, Cremers CW.

Ned Tijdschr Geneeskd. 2002 Dec 7;146(49):2354-8. Review. Dutch. PMID: 12510399 [PubMed - indexed for MEDLINE]Related articles

Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I.

Bharadwaj AK, Kasztejna JP, Huq S, Berson EL, Dryja TP.

Exp Eye Res. 2000 Aug;71(2):173-81.PMID: 10930322 [PubMed - indexed for MEDLINE]Related articles

Clinical and molecular genetics of Usher syndrome.

Kimberling WJ, Möller C.

J Am Acad Audiol. 1995 Jan;6(1):63-72.PMID: 7696679 [PubMed - indexed for MEDLINE]Related articles

Usher syndrome: definition and estimate of prevalence from two high-risk populations.

Boughman JA, Vernon M, Shaver KA.

J Chronic Dis. 1983;36(8):595-603.PMID: 6885960 [PubMed - indexed for MEDLINE]Related articles

Genetic heterogeneity of Usher syndrome type 1 in French families.

Larget-Piet D, Gerber S, Bonneau D, Rozet JM, Marc S, Ghazi I, Dufier JL, David A, Bitoun P, Weissenbach J, et al.

Genomics. 1994 May 1;21(1):138-43.PMID: 8088781 [PubMed - indexed for MEDLINE]Related articles

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

Astuto LM, Bork JM, Weston MD, Askew JW, Fields RR, Orten DJ, Ohliger SJ, Riazuddin S, Morell RJ, Khan S, Riazuddin S, Kremer H, van Hauwe P, Moller CG, Cremers CW, Ayuso C, Heckenlively JR, Rohrschneider K, Spandau U, Greenberg J, Ramesar R, Reardon W, Bitoun P, Millan J, Legge R, Friedman TB, Kimberling WJ.

Am J Hum Genet. 2002 Aug;71(2):262-75. Epub 2002 Jun 19.PMID: 12075507 [PubMed - indexed for MEDLINE]Related articlesFree article

A study of retinitis pigmentosa in the City of Birmingham. I Prevalence.

Bundey S, Crews SJ.

J Med Genet. 1984 Dec;21(6):417-20.PMID: 6512829 [PubMed - indexed for MEDLINE]Related articlesFree article

The ophthalmological course of Usher syndrome type III.

Pakarinen L, Tuppurainen K, Laippala P, Mäntyjärvi M, Puhakka H.

Int Ophthalmol. 1995-1996;19(5):307-11.PMID: 8864816 [PubMed - indexed for MEDLINE]Related articles

Usher syndrome: an otoneurologic study.

Möller CG, Kimberling WJ, Davenport SL, Priluck I, White V, Biscone-Halterman K, Odkvist LM, Brookhouser PE, Lund G, Grissom TJ.

Laryngoscope. 1989 Jan;99(1):73-9.PMID: 2909824 [PubMed - indexed for MEDLINE]Related articles

Ophthalmologic findings in Usher syndrome type 2A.

Van Aarem A, Wagenaar M, Pinckers AJ, Huygen PL, Bleeker-Wagemakers EM, Kimberling BJ, Cremers CW.

Ophthalmic Genet. 1995 Dec;16(4):151-8.PMID: 8749051 [PubMed - indexed for MEDLINE]Related articles

A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.

Liu XZ, Hope C, Liang CY, Zou JM, Xu LR, Cole T, Mueller RF, Bundey S, Nance W, Steel KP, Brown SD.

Am J Hum Genet. 1999 Apr;64(4):1221-5. No abstract available. PMID: 10090909 [PubMed - indexed for MEDLINE]Related articlesFree article

The prevalence of Usher syndrome and other retinal dystrophy-hearing impairment associations.

Rosenberg T, Haim M, Hauch AM, Parving A.

Clin Genet. 1997 May;51(5):314-21.PMID: 9212179 [PubMed - indexed for MEDLINE]Related articles

Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.

Ahmed ZM, Smith TN, Riazuddin S, Makishima T, Ghosh M, Bokhari S, Menon PS, Deshmukh D, Griffith AJ, Riazuddin S, Friedman TB, Wilcox ER.

Hum Genet. 2002 Jun;110(6):527-31. Epub 2002 May 3.PMID: 12107438 [PubMed - indexed for MEDLINE]Related articles

Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability.

Aller E, Jaijo T, Oltra S, Alió J, Galán F, Nájera C, Beneyto M, Millán JM.

Clin Genet. 2004 Dec;66(6):525-9.PMID: 15521980 [PubMed - indexed for MEDLINE]Related articles

Epidemiology of retinitis pigmentosa in Denmark.

Haim M.

Acta Ophthalmol Scand Suppl. 2002;(233):1-34.PMID: 11921605 [PubMed - indexed for MEDLINE]Related articles