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 *

153 related articles for article (PubMed ID: 8317638)

  • 1. [Usher syndrome. Two case reports].
    Adiego MI; Vallés H; Huerva V; Ascaso FJ; Iturbe F; Palomar A
    An Otorrinolaringol Ibero Am; 1993; 20(3):297-304. PubMed ID: 8317638
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [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]  

  • 4. 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]  

  • 5. [A case of Usher's syndrome associated with psychotic symptoms: diagnosis and follow-up in a psychiatric unit].
    Viala A; Nicot T; Levy F; Vacheron MN
    Encephale; 2009 Jun; 35(3):286-91. PubMed ID: 19540416
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Usher's syndrome and multiple sclerosis. Review of an individual with Usher's syndrome with a multiple sclerosis-like illness.
    Lynch SG; Digre K; Rose JW
    J Neuroophthalmol; 1994 Mar; 14(1):34-7. PubMed ID: 8032478
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Usher's syndrome type 3 in Finland.
    Pakarinen L; Karjalainen S; Simola KO; Laippala P; Kaitalo H
    Laryngoscope; 1995 Jun; 105(6):613-7. PubMed ID: 7769945
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The patient's view: Usher's syndrome.
    Can J Ophthalmol; 1980 Jan; 15(1):51-3. PubMed ID: 7378891
    [No Abstract]   [Full Text] [Related]  

  • 10. Is there genetic heterogeneity in Usher's syndrome?
    Matthews TW; Poliquin J; Mount J; MacFie D
    J Otolaryngol; 1987 Mar; 16(2):61-6. PubMed ID: 3599157
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. [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]  

  • 13. [Clinical examinations in Usher's syndrome].
    Lubiński W; Palacz O; Zajaczek S
    Klin Oczna; 1996 Jan; 98(1):55-8. PubMed ID: 9019578
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Usher's syndrome. Description of 3 cases].
    Kapuscinski WJ; Uher M; Ogielska E
    Bull Mem Soc Fr Ophtalmol; 1969; 82():147-51. PubMed ID: 5311799
    [No Abstract]   [Full Text] [Related]  

  • 15. [Usher's syndrome (association of familial pigmented retinopathy and deafness) 2 cases in a family].
    Michel M; Cotton JB; Picaud JJ; Lamit J; Destiné F; Freycon F
    Pediatrie; 1968 Dec; 23(8):948-51. PubMed ID: 5311102
    [No Abstract]   [Full Text] [Related]  

  • 16. [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]  

  • 17. Usher's syndrome with unusual otologic manifestations.
    Beatty CW; McDonald TJ; Colvard DM
    Mayo Clin Proc; 1979 Aug; 54(8):543-6. PubMed ID: 459566
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Perform vestibular test among all small deaf children! Early detection of Usher syndrome improves the possibilities of communication in the event of later deaf-blindness].
    Konrádsson K; Magnusson M; Andréasson S
    Lakartidningen; 1998 Jan; 95(5):379-81. PubMed ID: 9492482
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Usher's syndrome--case report.
    Kwiecień S; Sulak R; Szaflik J
    Klin Oczna; 2008; 110(10-12):384-6. PubMed ID: 19195172
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.