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Journal Abstract Search

579 related items for PubMed ID: 10807358

  • 1. Analysis of a cohort of children with sensory hearing loss using the SCALE systematic nomenclature.
    Sculerati N.
    Laryngoscope; 2000 May; 110(5 Pt 1):787-98. PubMed ID: 10807358
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  • 8. A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.
    Riahi Z, Chahed H, Jaafoura H, Zainine R, Messaoud O, Naili M, Nagara M, Hammami H, Laroussi N, Bouyacoub Y, Kefi R, Bonnet C, Besbes G, Abdelhak S.
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1485-8. PubMed ID: 23856379
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  • 9. Etiologic diagnosis of nonsyndromic genetic hearing loss in adult vs pediatric populations.
    King PJ, Ouyang X, Du L, Yan D, Angeli SI, Liu XZ.
    Otolaryngol Head Neck Surg; 2012 Nov; 147(5):932-6. PubMed ID: 22785241
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  • 10. Etiology of Childhood Bilateral Sensorineural Hearing Loss in Shandong Province, China.
    Jiang F, Kuper H, Bright T, Qin WZ.
    Am J Audiol; 2020 Jun 08; 29(2):236-243. PubMed ID: 32437266
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  • 13. A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members.
    Cesca F, Bettella E, Polli R, Cama E, Scimemi P, Santarelli R, Murgia A.
    Int J Pediatr Otorhinolaryngol; 2018 Jan 08; 104():88-93. PubMed ID: 29287889
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  • 14. Bilateral sensorineural hearing disorders in children: etiology of deafness and evaluation of hearing tests.
    Walch C, Anderhuber W, Köle W, Berghold A.
    Int J Pediatr Otorhinolaryngol; 2000 Jun 09; 53(1):31-8. PubMed ID: 10862922
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  • 15. Improved diagnostic effectiveness with a sequential diagnostic paradigm in idiopathic pediatric sensorineural hearing loss.
    Preciado DA, Lawson L, Madden C, Myer D, Ngo C, Bradshaw JK, Choo DI, Greinwald JH.
    Otol Neurotol; 2005 Jul 09; 26(4):610-5. PubMed ID: 16015155
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  • 19. Audiologic Phenotype and Progression in Pediatric STRC-Related Autosomal Recessive Hearing Loss.
    Simi A, Perry J, Schindler E, Oza A, Luo M, Hartman T, Krantz ID, Germiller JA, Kawai K, Kenna M.
    Laryngoscope; 2021 Dec 09; 131(12):E2897-E2903. PubMed ID: 34111299
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  • 20. [DNA diagnosis in congenital and early childhood hypoacusis and deafness].
    Markova TG, Megrelishvilli SM, Zaĭtseva NG, Shagina IA, Poliakov AV.
    Vestn Otorinolaringol; 2002 Dec 09; (6):12-5. PubMed ID: 12501766
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