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Journal Abstract Search
181 related items for PubMed ID: 8915413
1. 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 [Abstract] [Full Text] [Related]
2. 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 20; 59(3):375-9. PubMed ID: 8599365 [Abstract] [Full Text] [Related]
3. Prevalence and geographical distribution of Usher syndrome in Germany. Spandau UH, Rohrschneider K. Graefes Arch Clin Exp Ophthalmol; 2002 Jun 20; 240(6):495-8. PubMed ID: 12107518 [Abstract] [Full Text] [Related]
4. Early diagnosis of Usher syndrome in children. Mets MB, Young NM, Pass A, Lasky JB. Trans Am Ophthalmol Soc; 2000 Jun 20; 98():237-42; discussion 243-5. PubMed ID: 11190026 [Abstract] [Full Text] [Related]
5. 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 01; 50(1):32-8. PubMed ID: 8160750 [Abstract] [Full Text] [Related]
6. 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 01; 7(3):363-7. PubMed ID: 10234513 [Abstract] [Full Text] [Related]
8. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies. Zwirner P, Wilichowski E. Laryngoscope; 2001 Mar 01; 111(3):515-21. PubMed ID: 11224785 [Abstract] [Full Text] [Related]
9. Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients. Plantinga RF, Kleemola L, Huygen PL, Joensuu T, Sankila EM, Pennings RJ, Cremers CW. Audiol Neurootol; 2005 Mar 01; 10(2):79-89. PubMed ID: 15650299 [Abstract] [Full Text] [Related]
10. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene. Bravo O, Ballana E, Estivill X. Biochem Biophys Res Commun; 2006 Jun 02; 344(2):511-6. PubMed ID: 16631122 [Abstract] [Full Text] [Related]
11. Comparative study of visual, auditory, and olfactory function in Usher syndrome. Seeliger M, Pfister M, Gendo K, Paasch S, Apfelstedt-Sylla E, Plinkert P, Zenner HP, Zrenner E. Graefes Arch Clin Exp Ophthalmol; 1999 Apr 02; 237(4):301-7. PubMed ID: 10208263 [Abstract] [Full Text] [Related]
12. Hearing loss in Usher syndrome type II is nonprogressive. Reisser CF, Kimberling WJ, Otterstedde CR. Ann Otol Rhinol Laryngol; 2002 Dec 02; 111(12 Pt 1):1108-11. PubMed ID: 12498372 [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 07; 146(49):2354-8. PubMed ID: 12510399 [Abstract] [Full Text] [Related]
14. Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family. Plantinga RF, Cremers CW, Huygen PL, Kunst HP, Bosman AJ. J Assoc Res Otolaryngol; 2007 Mar 07; 8(1):1-7. PubMed ID: 17136632 [Abstract] [Full Text] [Related]
15. Cochlear function in facioscapulohumeral muscular dystrophy. Balatsouras DG, Korres S, Manta P, Panousopoulou A, Vassilopoulos D. Otol Neurotol; 2007 Jan 07; 28(1):7-10. PubMed ID: 17106430 [Abstract] [Full Text] [Related]
16. Evaluation of cochlear involvement by distortion product otoacoustic emission in Behçet's disease. Dagli M, Eryilmaz A, Tanrikulu S, Aydin A, Gonul M, Gul U, Gocer C. Auris Nasus Larynx; 2008 Sep 07; 35(3):333-7. PubMed ID: 17996415 [Abstract] [Full Text] [Related]
17. [Acoustic distortion product recording in patients with sensorineural hearing loss]. Pérez del Valle B, Morant Ventura A, Contreras Castelló A, Orts Albors M, Marco Algarra J. Acta Otorrinolaringol Esp; 1996 Sep 07; 47(2):111-8. PubMed ID: 8695198 [Abstract] [Full Text] [Related]
18. 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 07; 24(2):102-4. PubMed ID: 7602669 [Abstract] [Full Text] [Related]
19. Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation. Tamagawa Y, Ishikawa K, Ishikawa K, Ishida T, Kitamura K, Makino S, Tsuru T, Ichimura K. Laryngoscope; 2002 Feb 07; 112(2):292-7. PubMed ID: 11889386 [Abstract] [Full Text] [Related]
20. Familial auditory neuropathy. Wang Q, Gu R, Han D, Yang W. Laryngoscope; 2003 Sep 07; 113(9):1623-9. PubMed ID: 12972945 [Abstract] [Full Text] [Related] Page: [Next] [New Search]