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

Usher syndromes due to MY07A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanismJACOBSON, Samuel G; CIDECIYAN, Artur V; SCHWARTZ, Sharon B et al.Human molecular genetics (Print). 2008, Vol 17, Num 15, pp 2405-2415, issn 0964-6906, 11 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

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

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

Retinal Disease in Usher Syndrome III Caused by Mutations in the Clarin-1 GeneHERRERA, Waldo; ALEMAN, Tomas S; STONE, Edwin M et al.Investigative ophthalmology & visual science. 2008, Vol 49, Num 6, pp 2651-2660, issn 0146-0404, 10 p.Article

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

Usher's syndrome, temporal bone pathologyCREMERS, C. W. R. JR; DELLEMAN, W. J. W.International journal of pediatric otorhinolaryngology. 1988, Vol 16, Num 1, pp 23-30, issn 0165-5876Article

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

Disease Boundaries in the Retina of Patients with Usher Syndrome Caused by MY07A Gene MutationsJACOBSON, Samuel G; ALEMAN, Tomas S; SUMAROKA, Alexander et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 4, pp 1886-1894, issn 0146-0404, 9 p.Article

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type IIWESTON, Michael D; LUIJENDIJK, Mirjam W. J; HUMPHREY, Kurt D et al.American journal of human genetics. 2004, Vol 74, Num 2, pp 357-366, issn 0002-9297, 10 p.Article

Hearing loss in Usher syndrome type II is nonprogressiveREISSER, Christoph F. V; KIMBERLING, William J; OTTERSTEDDE, Christian R et al.The Annals of otology, rhinology & laryngology. 2002, Vol 111, Num 12, pp 1108-1111, issn 0003-4894, 4 p., 1Article

The Usher syndrome type 2A : clinical findings in obligate carriersVAN AAREM, A; CREMERS, C. W. R. J; PINCKERS, A. J. L. G et al.International journal of pediatric otorhinolaryngology. 1995, Vol 31, Num 2-3, pp 159-174, issn 0165-5876Article

Sarcosinaemia in a patient with Usher syndromeCHRISTENSEN, E; BRANDT, N. J; ROSENBERG, T et al.Journal of inherited metabolic disease. 1989, Vol 12, Num 4, pp 487-488, issn 0141-8955Article

Screening of school-aged hearing impaired childrenROGERS, G. L; FILLMAN, R. D; BREMER, D. L et al.Journal of pediatric ophthalmology and strabismus. 1988, Vol 25, Num 5, pp 230-232, issn 0191-3913Article