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4. [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; 146(49):2354-8. PubMed ID: 12510399 [TBL] [Abstract][Full Text] [Related]
5. Usher syndrome in four siblings from a consanguineous family of Pakistani origin. Trop I; Schloss MD; Polomeno R; Der Kaloustian V J Otolaryngol; 1995 Apr; 24(2):102-4. PubMed ID: 7602669 [TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 15521980 [TBL] [Abstract][Full Text] [Related]
7. Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium. Smith RJ; Berlin CI; Hejtmancik JF; Keats BJ; Kimberling WJ; Lewis RA; Möller CG; Pelias MZ; Tranebjaerg L Am J Med Genet; 1994 Mar; 50(1):32-8. PubMed ID: 8160750 [TBL] [Abstract][Full Text] [Related]
9. A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2. Hmani M; Ghorbel A; Boulila-Elgaied A; Ben Zina Z; Kammoun W; Drira M; Chaabouni M; Petit C; Ayadi H Eur J Hum Genet; 1999 Apr; 7(3):363-7. PubMed ID: 10234513 [TBL] [Abstract][Full Text] [Related]
11. Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2). Beneyto MM; Cuevas JM; Millán JM; Espinós C; Mateu E; González-Cabo P; Baiget M; Doménech M; Bernal S; Ayuso C; García-Sandoval B; Trujillo MJ; Borrego S; Antiñolo G; Carballo M; Nájera C Ophthalmic Genet; 2000 Jun; 21(2):123-8. PubMed ID: 10916187 [TBL] [Abstract][Full Text] [Related]
12. Spectrum of mutations in USH2A in British patients with Usher syndrome type II. Leroy BP; Aragon-Martin JA; Weston MD; Bessant DA; Willis C; Webster AR; Bird AC; Kimberling WJ; Payne AM; Bhattacharya SS Exp Eye Res; 2001 May; 72(5):503-9. PubMed ID: 11311042 [TBL] [Abstract][Full Text] [Related]
13. Screening of the USH1G gene among Spanish patients with Usher syndrome. Lack of mutations and evidence of a minor role in the pathogenesis of the syndrome. Aller E; Jaijo T; Beneyto M; Nájera C; Morera C; Pérez-Garrigues H; Ayuso C; Millán J Ophthalmic Genet; 2007 Sep; 28(3):151-5. PubMed ID: 17896313 [TBL] [Abstract][Full Text] [Related]
14. Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D. von Brederlow B; Bolz H; Janecke A; La O Cabrera A; Rudolph G; Lorenz B; Schwinger E; Gal A Hum Mutat; 2002 Mar; 19(3):268-73. PubMed ID: 11857743 [TBL] [Abstract][Full Text] [Related]
15. Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older. Grover S; Fishman GA; Anderson RJ; Tozatti MS; Heckenlively JR; Weleber RG; Edwards AO; Brown J Ophthalmology; 1999 Sep; 106(9):1780-5. PubMed ID: 10485550 [TBL] [Abstract][Full Text] [Related]
16. Early diagnosis of Usher syndrome in children. Mets MB; Young NM; Pass A; Lasky JB Trans Am Ophthalmol Soc; 2000; 98():237-42; discussion 243-5. PubMed ID: 11190026 [TBL] [Abstract][Full Text] [Related]
17. Prevalence and geographical distribution of Usher syndrome in Germany. Spandau UH; Rohrschneider K Graefes Arch Clin Exp Ophthalmol; 2002 Jun; 240(6):495-8. PubMed ID: 12107518 [TBL] [Abstract][Full Text] [Related]
18. A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25. Mustapha M; Chouery E; Torchard-Pagnez D; Nouaille S; Khrais A; Sayegh FN; Mégarbané A; Loiselet J; Lathrop M; Petit C; Weil D Hum Genet; 2002 Apr; 110(4):348-50. PubMed ID: 11941484 [TBL] [Abstract][Full Text] [Related]
19. Usher's syndrome and multiple sclerosis. Review of an individual with Usher's syndrome with a multiple sclerosis-like illness. Lynch SG; Digre K; Rose JW J Neuroophthalmol; 1994 Mar; 14(1):34-7. PubMed ID: 8032478 [TBL] [Abstract][Full Text] [Related]
20. [A case of Usher's syndrome associated with psychotic symptoms: diagnosis and follow-up in a psychiatric unit]. Viala A; Nicot T; Levy F; Vacheron MN Encephale; 2009 Jun; 35(3):286-91. PubMed ID: 19540416 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]