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 *

63 related articles for article (PubMed ID: 2036256)

  • 1. [Usher syndrome. A genetic, otoneurologic and ophthalmologic study].
    Giménez Vaillo F; Grimaldos Ruiz P; Marco Algarra J; Ivorra Lahuerta P; Montalt J
    Acta Otorrinolaringol Esp; 1991; 42(1):13-9. PubMed ID: 2036256
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [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]  

  • 4. [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]  

  • 5. [Hereditary maculopathy in typical retinitis pigmentosa. Apropos of 40 cases].
    Chachia N; Romdane K; Zaghdane M; Hadj Hamida FB; Khayrallah M; Haddad M
    Ophtalmologie; 1989; 3(1):67-8. PubMed ID: 2641075
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 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. 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]  

  • 9. 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; 7(3):363-7. PubMed ID: 10234513
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Schizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness.
    Sharp CW; Muir WJ; Blackwood DH; Walker M; Gosden C; St Clair DM
    Am J Med Genet; 1994 Dec; 54(4):354-60. PubMed ID: 7726208
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D.
    von Brederlow B; Bolz H; Janecke A; La O Cabrera A; Rudolph G; Lorenz B; Schwinger E; Gal A
    Hum Mutat; 2002 Mar; 19(3):268-73. PubMed ID: 11857743
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early diagnosis of Usher syndrome in infants and children.
    Young NM; Mets MB; Hain TC
    Am J Otol; 1996 Jan; 17(1):30-4. PubMed ID: 8694131
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 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. [Electrophysiologic tests of the auditory apparatus and vestibular organ in Usher syndrome].
    Pośpiech L; Gawron W; Rostkowska-Nadolska B; Koziorowska M
    Otolaryngol Pol; 2003; 57(1):121-6. PubMed ID: 12741156
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and genetic studies in Spanish patients with Usher syndrome type II: description of new mutations and evidence for a lack of genotype--phenotype correlation.
    Bernal S; Medà C; Solans T; Ayuso C; Garcia-Sandoval B; Valverde D; Del Rio E; Baiget M
    Clin Genet; 2005 Sep; 68(3):204-14. PubMed ID: 16098008
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.