These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 7696679)

  • 1. Clinical and molecular genetics of Usher syndrome.
    Kimberling WJ; Möller C
    J Am Acad Audiol; 1995 Jan; 6(1):63-72. PubMed ID: 7696679
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Cochleo-vestibular manifestations in retinitis pigmentosa (Usher's syndrome)].
    Torres G; Kume M; Corvera J; Prado A
    Acta Otorinolaryngol Iber Am; 1972; 23(4):517-24. PubMed ID: 4539456
    [No Abstract]   [Full Text] [Related]  

  • 3. Usher syndrome in four hard-of-hearing siblings.
    Davenport SL; O'Nuallain S; Omenn GS; Wilkus RJ
    Pediatrics; 1978 Oct; 62(4):578-83. PubMed ID: 714590
    [TBL] [Abstract][Full Text] [Related]  

  • 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. 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]  

  • 6. Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome.
    Hmani-Aifa M; Ben Arab S; Kharrat K; Orten DJ; Boulila-Elgaied A; Drira M; Hachicha S; Kimberling WJ; Ayadi H
    J Med Genet; 2002 Apr; 39(4):281-3. PubMed ID: 11950859
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Genetic heterogeneity of Usher syndrome type II in a Dutch population.
    Pieke-Dahl S; van Aarem A; Dobin A; Cremers CW; Kimberling WJ
    J Med Genet; 1996 Sep; 33(9):753-7. PubMed ID: 8880575
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
    Astuto LM; Bork JM; Weston MD; Askew JW; Fields RR; Orten DJ; Ohliger SJ; Riazuddin S; Morell RJ; Khan S; Riazuddin S; Kremer H; van Hauwe P; Moller CG; Cremers CW; Ayuso C; Heckenlively JR; Rohrschneider K; Spandau U; Greenberg J; Ramesar R; Reardon W; Bitoun P; Millan J; Legge R; Friedman TB; Kimberling WJ
    Am J Hum Genet; 2002 Aug; 71(2):262-75. PubMed ID: 12075507
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Usher syndrome type III can mimic other types of Usher syndrome.
    Pennings RJ; Fields RR; Huygen PL; Deutman AF; Kimberling WJ; Cremers CW
    Ann Otol Rhinol Laryngol; 2003 Jun; 112(6):525-30. PubMed ID: 12834121
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Usher syndrome type I associated with bronchiectasis and immotile nasal cilia in two brothers.
    Bonneau D; Raymond F; Kremer C; Klossek JM; Kaplan J; Patte F
    J Med Genet; 1993 Mar; 30(3):253-4. PubMed ID: 8474110
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.
    Reiners J; Nagel-Wolfrum K; Jürgens K; Märker T; Wolfrum U
    Exp Eye Res; 2006 Jul; 83(1):97-119. PubMed ID: 16545802
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Localization of Usher syndrome type II to chromosome 1q.
    Kimberling WJ; Weston MD; Möller C; Davenport SL; Shugart YY; Priluck IA; Martini A; Milani M; Smith RJ
    Genomics; 1990 Jun; 7(2):245-9. PubMed ID: 2347588
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Molecular updates on Usher syndrome].
    Roux AF
    J Fr Ophtalmol; 2005 Jan; 28(1):93-7. PubMed ID: 15767904
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Syndromic hereditary deafness. Usher's syndrome. Oto-neurologic and genetic factors].
    Espinós C; Pérez-Garrigues H; Beneyto M; Vilela C; Rodrigo O; Nájera C
    An Otorrinolaringol Ibero Am; 1999; 26(1):83-95. PubMed ID: 10091368
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.
    Ebermann I; Scholl HP; Charbel Issa P; Becirovic E; Lamprecht J; Jurklies B; Millán JM; Aller E; Mitter D; Bolz H
    Hum Genet; 2007 Apr; 121(2):203-11. PubMed ID: 17171570
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I.
    Otterstedde CR; Spandau U; Blankenagel A; Kimberling WJ; Reisser C
    Laryngoscope; 2001 Jan; 111(1):84-6. PubMed ID: 11192904
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Gene mapping of the Usher syndromes.
    Kimberling W; Smith RJ
    Otolaryngol Clin North Am; 1992 Oct; 25(5):923-34. PubMed ID: 1408196
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.