209 related articles for article (PubMed ID: 12107518)
1. 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]
2. 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]
3. 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]
4. Novel mutations in MYO7A and USH2A in Usher syndrome.
Maubaret C; Griffoin JM; Arnaud B; Hamel C
Ophthalmic Genet; 2005 Mar; 26(1):25-9. PubMed ID: 15823922
[TBL] [Abstract][Full Text] [Related]
5. Carriers of the Usher syndrome type IB: is audiometric identification possible?
Wagenaar M; Snik AF; Kimberling WJ; Cremers CW
Am J Otol; 1996 Nov; 17(6):853-8. PubMed ID: 8915413
[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]
8. 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]
9. 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. PubMed ID: 15236894
[TBL] [Abstract][Full Text] [Related]
10. Identification of candidate regions for a novel Usher syndrome type II locus.
Ben Rebeh I; Benzina Z; Dhouib H; Hadjamor I; Amyere M; Ayadi L; Turki K; Hammami B; Kmiha N; Kammoun H; Hakim B; Charfedine I; Vikkula M; Ghorbel A; Ayadi H; Masmoudi S
Mol Vis; 2008 Sep; 14():1719-26. PubMed ID: 18806881
[TBL] [Abstract][Full Text] [Related]
11. Usher syndrome: clinical findings and gene localization studies.
Kimberling WJ; Möller CG; Davenport SL; Lund G; Grissom TJ; Priluck I; White V; Weston MD; Biscone-Halterman K; Brookhouser PE
Laryngoscope; 1989 Jan; 99(1):66-72. PubMed ID: 2562904
[TBL] [Abstract][Full Text] [Related]
12. Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study.
Stingl K; Kurtenbach A; Hahn G; Kernstock C; Hipp S; Zobor D; Kohl S; Bonnet C; Mohand-Saïd S; Audo I; Fakin A; Hawlina M; Testa F; Simonelli F; Petit C; Sahel JA; Zrenner E
Doc Ophthalmol; 2019 Oct; 139(2):151-160. PubMed ID: 31267413
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Hearing loss in Usher syndrome type II is nonprogressive.
Reisser CF; Kimberling WJ; Otterstedde CR
Ann Otol Rhinol Laryngol; 2002 Dec; 111(12 Pt 1):1108-11. PubMed ID: 12498372
[TBL] [Abstract][Full Text] [Related]
15. Quality of life and cochlear implantation in Usher syndrome type I.
Damen GW; Pennings RJ; Snik AF; Mylanus EA
Laryngoscope; 2006 May; 116(5):723-8. PubMed ID: 16652078
[TBL] [Abstract][Full Text] [Related]
16. [Molecular updates on Usher syndrome].
Roux AF
J Fr Ophtalmol; 2005 Jan; 28(1):93-7. PubMed ID: 15767904
[TBL] [Abstract][Full Text] [Related]
17. Clinical findings in obligate carriers of type I Usher syndrome.
Wagenaar M; ter Rahe B; van Aarem A; Huygen P; Admiraal R; Bleeker-Wagemakers E; Pinckers A; Kimberling W; Cremers C
Am J Med Genet; 1995 Nov; 59(3):375-9. PubMed ID: 8599365
[TBL] [Abstract][Full Text] [Related]
18. Usher syndrome: results of a screening program in Colombia.
Tamayo ML; Bernal JE; Tamayo GE; Frias JL; Alvira G; Vergara O; Rodriguez V; Uribe JI; Silva JC
Clin Genet; 1991 Oct; 40(4):304-11. PubMed ID: 1756603
[TBL] [Abstract][Full Text] [Related]
19. [The incidence of Usher's syndrome and its clinical types].
Bereketoğlu M; Avşar EU; Turan O; Afrashi F; Apaydin F
Kulak Burun Bogaz Ihtis Derg; 2002; 9(1):15-20. PubMed ID: 12122620
[TBL] [Abstract][Full Text] [Related]
20. 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. PubMed ID: 2909824
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
