An unusual otological manifestation of Usher's syndrome in four siblingsKARJALAINEN, S; TERÄSVIRTA, M; KÄRJA, J et al.Clinical genetics. 1983, Vol 24, Num 4, pp 273-279, issn 0009-9163Article

Usher Syndrom, eine erbliche Hör-Sehschädigung = Le syndrome d'Usher, une lésion héréditaire de l'ouïe et de la vue = Usher's syndrome, an hereditary lesion of listering and visionBUNCK, D.Sprache, Stimme. Gehör. 1987, Vol 11, Num 3, pp 109-111, issn 0342-0477Article

GENETIC COUNSELING IN CONGENITAL EYE DISORDERSBOHAR A; CZEIZEL A.1983; OPHTHALMOLOGICA (BASEL); ISSN 0030-3755; CHE; DA. 1983; VOL. 187; NO 3; PP. 174-180; ABS. FRE/GER; BIBL. 10 REF.Article

VISUAL LOSS AND FOVEAL LESIONS IN USHER'S SYNDROMEFISHMAN G; VASQUEZ V; FISHMAN M et al.1979; BRIT. J. OPHTHALMOL.; GBR; DA. 1979; VOL. 63; NO 7; PP. 484-488; BIBL. 8 REF.Article

THE PATIENT'S VIEW: USHER'S SYNDROME1980; CANAD. J. OPHTHALMOL.; CAN; DA. 1980; VOL. 15; NO 1; PP. 51-53; ABS. FREArticle

USHER'S SYNDROME TYPE IIIGORLIN RJ; TILSNER TJ; FEINSTEIN S et al.1979; ARCH. OTOLARYNGOL.; USA; DA. 1979; VOL. 105; NO 6; PP. 353-354; BIBL. 7 REF.Article

CURRENT SCREENING PROCEDURES FOR THE USHER SYNDROME AT RESIDENTIAL SCHOOLS FOR THE DEAFDAY CW.1982; AM. ANN. DEAF (WASH. 1886); ISSN 0002-726X; USA; DA. 1982; VOL. 127; NO 1; PP. 45-48; BIBL. 8 REF.Article

Quality of life and cochlear implantation in usher syndrome type IDAMEN, Godelieve W. J. A; PENNINGS, Ronald J. E; SNIK, Ad F. M et al.The Laryngoscope. 2006, Vol 116, Num 5, pp 723-728, issn 0023-852X, 6 p.Article

Audiologic performance and benefit of cochlear implantation in usher syndrome type IPENNINGS, Ronald J. E; DAMEN, Godelieve W. J. A; SNIK, Ad F. M et al.The Laryngoscope. 2006, Vol 116, Num 5, pp 717-722, issn 0023-852X, 6 p.Article

Usher syndrome : molecular links of pathogenesis, proteins and pathwaysKREMER, Hannie; VAN WIJK, Erwin; MÄRKER, Tina et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R262-R270, NS2Article

Interactions in the network of Usher syndrome type 1 proteinsADATO, Avital; MICHEL, Vincent; KIKKAWA, Yoshiaki et al.Human molecular genetics (Print). 2005, Vol 14, Num 3, pp 347-356, issn 0964-6906, 10 p.Article

Usher syndrome type 1 associated with primary ciliary aplasiaTOSI, Gian Marco; DE SANTI, Maria Margherita; PRADAL, Ugo et al.Archives of ophthalmology (1960). 2003, Vol 121, Num 3, pp 407-408, issn 0003-9950, 2 p.Article

Retinitis pigmentosa and progressive hearning lossKARP, A; SANTORE, F.The Journal of speech and hearing disorders. 1983, Vol 48, Num 3, pp 308-314, issn 0022-4677Article

Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2REINERS, Jan; VAN WIJK, Erwin; WOLFRUM, Uwe et al.Human molecular genetics (Print). 2005, Vol 14, Num 24, pp 3933-3943, issn 0964-6906, 11 p.Article

Radiation sensitivity of fibroblast strains from patients with Usher's syndrome, Duchenne muscular dystrophy, and Huntington's diseaseNOVE, J; TARONE, R. E; LITTLE, J. B et al.Mutation research. 1987, Vol 184, Num 1, pp 29-38, issn 0027-5107Article

Giant retinal tears, retinal detachment and retinitis pigmentosaJOHNSTON, M. E; GONDER, J. R.Canadian journal of ophthalmology. 1985, Vol 20, Num 1, pp 16-18, issn 0008-4182Article

Usher syndrome type III can mimic other types of Usher syndromePENNINGS, Ronald J. E; FIELDS, Randall R; HUYGEN, Patrick L. M et al.The Annals of otology, rhinology & laryngology. 2003, Vol 112, Num 6, pp 525-530, issn 0003-4894, 6 p.Article

Les syndrome de Usher : aspects ophtalmologiques = Usher's syndrome :ophtalmological aspectsRISSE, J.-F; BONNEAU, D; RAYMOND, F et al.Bulletin des sociétés d'ophtalmologie de France. 1995, Vol 95, Num 5, pp 372-376, issn 0081-1270Article

Usher syndrome: an otoneurologic studyMÖLLER, C. G; KIMBERLING, W. J; DAVENPORT, S. L. H et al.The Laryngoscope. 1989, Vol 99, Num 1, pp 73-79, issn 0023-852XArticle

Usher syndrome: clinical findings and gene localization studiesKIMBERLING, W. J; MÖLLER, C. G; DAVENPORT, S. L. H et al.The Laryngoscope. 1989, Vol 99, Num 1, pp 66-72, issn 0023-852XArticle

Development of a genotyping microarray for Usher syndromeCREMERS, Frans P. M; KIMBERLING, William J; FLEISCHHAUER, Johannes C et al.Journal of medical genetics. 2007, Vol 44, Num 2, pp 153-160, issn 0022-2593, 8 p.Article

First evidence for a molecular link between Usher 1 and Usher 2 syndromesSTEIN, R. A.Clinical genetics. 2006, Vol 69, Num 6, pp 483-485, issn 0009-9163, 3 p.Article

Mutational spectrum in Usher syndrome type IIOUYANG, X. M; YAM, D; HEJTMANCIK, J. F et al.Clinical genetics. 2004, Vol 65, Num 4, pp 288-293, issn 0009-9163, 6 p.Article

Case report : retinitis pigmentosa following cytotoxic chemotherapy in Usher's syndromeBLANCHET, P; WELLEMEYER, M. L; BURTON, G. V et al.The American journal of the medical sciences. 1992, Vol 303, Num 5, pp 319-320, issn 0002-9629Article

Innervation densities of inner and outer hair cells of the human organ of Corti: evidence for auditory neural degeneration in a case of Usher's syndromeNADOL, J. B. JR.ORL. 1988, Vol 50, Num 6, pp 363-370, issn 0301-1569Article