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La ricerca find articoli where soggetti phrase all words 'hearing loss' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 2612 riferimenti
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    1. Ziegler, EA; Bohl, J; Maurer, J
      Bilateral hearing loss as first symptom of a carcinoma of the pancreas.

      LARYNGO-RHINO-OTOLOGIE
    2. Acham, A; Walch, C
      Mondini dysplasia without functional impairment in a case of CHARGE association.

      LARYNGO-RHINO-OTOLOGIE
    3. Naumann, A; Hempel, JM; Schorn, K
      Humoral immune response to inner ear proteins in patients with sensorineural hearing loss.

      LARYNGO-RHINO-OTOLOGIE
    4. Schonweiler, B; Held, M; Schonweiler, R
      A case report of cochlear hearing loss following an infection with mycoplasma pneumoniae.

      LARYNGO-RHINO-OTOLOGIE
    5. Bachor, E; Karmody, CS
      Retraction of the endolymphatic membranes in temporal bones of the Wittmack and Tufts collection.

      LARYNGO-RHINO-OTOLOGIE
    6. Klask, J
      Injuries of ear nose and throat caused by airbag deployment.

      LARYNGO-RHINO-OTOLOGIE
    7. Kiese-Himmel, C; Kruse, E
      Unilateral hearing loss in children - An empirical analysis in comparison with bilateral hearing impairment.

      LARYNGO-RHINO-OTOLOGIE
    8. Nia, J; Bance, M
      Effects of varying unilateral conductive hearing losses on speech-in-noisediscrimination: An experimental study with implications for surgical correction

      OTOLOGY & NEUROTOLOGY
    9. Schick, B; Brors, D; Koch, O; Schafers, M; Kahle, G
      Magnetic resonance imaging in patients with sudden hearing loss, tinnitus and vertigo

      OTOLOGY & NEUROTOLOGY
    10. Govaerts, PJ; Yperman, M; De Ceulaer, G; Daemers, K; Van Driessche, K; Somers, T; Offeciers, FE
      A two-stage bipodal screening model for universal neonatal hearing screening

      OTOLOGY & NEUROTOLOGY
    11. Dhooge, I; Lantsoght, B; Lemmerling, M; Vanzieleghem, B; Mortier, G
      Hearing loss as a presenting symptom of cleidocranial dysplasia

      OTOLOGY & NEUROTOLOGY
    12. Kudo, T; Ikeda, K; Oshima, T; Kure, S; Tammasaeng, M; Prasansuk, S; Matsubara, Y
      GJB2 (connexin 26) mutations and childhood deafness in Thailand

      OTOLOGY & NEUROTOLOGY
    13. Verstreken, M; Declau, F; Wuyts, FL; D'Haese, P; Van Camp, G; Fransen, E; Van den Hauwe, L; Buyle, S; Smets, REM; Feenstra, L; Van der Stappen, A; Van de Heyning, PH
      Hereditary otovestibular dysfunction and Meniere's disease in a large Belgian family is caused by a missense mutation in the COCH gene

      OTOLOGY & NEUROTOLOGY
    14. Brackmann, DE; Kesser, BW; Day, JD
      Microvascular decompression of the vestibulocochlear nerve for disabling positional vertigo: The house ear clinic experience

      OTOLOGY & NEUROTOLOGY
    15. Fraysse, B; Lavieille, JP; Schmerber, S; Enee, V; Truy, E; Vincent, C; Vaneecloo, FM; Sterkers, O
      A multicenter study of the vibrant soundbridge middle ear implant: Early clinical results and experience

      OTOLOGY & NEUROTOLOGY
    16. Declau, F; Van Spaendonck, M; Timmermans, JP; Michaels, L; Liang, J; Qiu, JP; Van de Heyning, P
      Prevalence of otosclerosis in an unselected series of temporal bones

      OTOLOGY & NEUROTOLOGY
    17. Boulassel, MR; Tomasi, JP; Deggouj, N; Gersdorff, M
      COCH5B2 is a target antigen of anti-inner ear antibodies in autoimmune inner ear diseases

      OTOLOGY & NEUROTOLOGY
    18. Rahman, MU; Poe, DS; Choi, HK
      Etanercept therapy for immune-mediated cochleovestibular disorders: Preliminary results in a pilot study

      OTOLOGY & NEUROTOLOGY
    19. Kemperman, MH; Stinckens, C; Kumar, S; Huygen, PLM; Joosten, FBM; Cremers, CWRJ
      Progressive fluctuant hearing loss, enlarged vestibular aqueduct, and cochlear hypoplasia in branchio-oto-renal syndrome

      OTOLOGY & NEUROTOLOGY
    20. Badie, B; Pyle, GM; Nguyen, PH; Hadar, EJ
      Elevation of internal auditory canal pressure by vestibular schwannomas

      OTOLOGY & NEUROTOLOGY
    21. Kopke, RD; Hoffer, ME; Wester, D; O'Leary, MJ; Jackson, RL
      Targeted topical steroid therapy in sudden sensorineural hearing loss

      OTOLOGY & NEUROTOLOGY
    22. Sargent, EW; Herrmann, B; Kollenbeak, CS; Bankaitis, AE
      The minimum speech test battery in profound unilateral hearing loss

      OTOLOGY & NEUROTOLOGY
    23. Bamiou, DE; Worth, S; Phelps, P; Sirimanna, T; Rajput, K
      Eighth nerve aplasia and hypoplasia in cochlear implant candidates: The clinical perspective

      OTOLOGY & NEUROTOLOGY
    24. Merchany, SN; McKenna, MJ; Nadol, JB; Kristiansen, AG; Tropitzsch, A; Lindal, S; Tranebjaerg, L
      Temporal bone histopathologic and genetic studies in Mohr-Tranebj rg syndrome (DFN-1)

      OTOLOGY & NEUROTOLOGY
    25. Soderman, ACH; Bergenius, J; Bagger-Sjoback, D; Tjell, C; Langius, A
      Patients' subjective evaluations of quality of life related to disease-specific symptoms, sense of coherence, and treatment in Meniere's disease

      OTOLOGY & NEUROTOLOGY
    26. Lustig, LR; Arts, HA; Brackmann, DE; Francis, HF; Molony, T; Megerian, CA; Moore, GF; Moore, KM; Morrow, T; Potsic, W; Rubenstein, JT; Srireddy, S; Syms, CA; Takahashi, G; Vernick, D; Wackym, PA; Niparko, JK
      Hearing rehabilitation using the BAHA bone-anchored hearing aid: Results in 40 patients

      OTOLOGY & NEUROTOLOGY
    27. Buckmiller, LM; Brodie, HA; Doyle, KJ; Nemzek, W
      Choristoma of the middle ear: A component of a new syndrome?

      OTOLOGY & NEUROTOLOGY
    28. Young, YH; Lin, CY; Lou, PJ; Hsu, MM
      Intracranial relapse of nasopharyngeal carcinoma manifested as sudden deafness

      OTOLOGY & NEUROTOLOGY
    29. Saito, T; Tanaka, T; Tokuriki, M; Shibamori, Y; Yamamoto, T; Noda, I; Ohtsubo, T; Saito, H
      Recent outcome of tympanoplasty in the elderly

      OTOLOGY & NEUROTOLOGY
    30. Nadol, JB
      Histopathology of residual and recurrent conductive hearing loss after stapedectomy

      OTOLOGY & NEUROTOLOGY
    31. Chole, RA; McKenna, M
      Pathophysiology of otosclerosis

      OTOLOGY & NEUROTOLOGY
    32. Chandrasekhar, SS
      Intratympanic dexamethasone for sudden sensorineural hearing loss: Clinical and laboratory evaluation

      OTOLOGY & NEUROTOLOGY
    33. Rabinowitz, PM; Duran, R
      Is acculturation related to use of hearing protection?

      AIHAJ
    34. Seixas, NS; Ren, K; Neitzel, R; Camp, J; Yost, M
      Noise exposure among construction electricians

      AIHAJ
    35. Petit, C
      Usher syndrome: From genetics to pathogenesis

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    36. Jimenez, AM; Stagner, BB; Martin, GK; Lonsbury-Martin, BL
      Susceptibility of DPOAEs to sound overexposure in inbred mice with AHL

      JARO
    37. Hequembourg, S; Liberman, MC
      Spiral ligament pathology: A major aspect of age-related cochlear degeneration in C57BL/6 mice

      JARO
    38. Griffiths, TD; Blakemore, S; Elliott, C; Moore, BCJ; Chinnery, PF
      Psychophysical evaluation of cochlear hair cell damage due to the A3243G mitochondrial DNA mutation

      JARO
    39. Chen, XW; Frisina, RD; Bowers, WJ; Frisina, DR; Federoff, HJ
      HSV amplicon-mediated neurotrophin-3 expression protects murine spiral ganglion neurons from cisplatin-induced damage

      MOLECULAR THERAPY
    40. Scherer, A; Engelbrecht, V; Nawatny, J; Messing-Junger, M; Reifenberger, G; Modder, U
      MRI of the cerebellopontine angle in patients with cleido-cranial dysostosis

      ROFO-FORTSCHRITTE AUF DEM GEBIET DER RONTGENSTRAHLEN UND DER BILDGEBENDEN VERFAHREN
    41. Akita, J; Abe, S; Shinkawa, H; Kimberling, WJ; Usami, S
      Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese

      JOURNAL OF HUMAN GENETICS
    42. Nagata, H; Kumahara, K; Tomemori, T; Arimoto, Y; Isoyama, K; Yoshida, K; Konno, A
      Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics

      JOURNAL OF HUMAN GENETICS
    43. Irvine, DRF; Rajan, R; Brown, M
      Injury- and use-related plasticity in adult auditory cortex

      AUDIOLOGY AND NEURO-OTOLOGY
    44. Moore, DR; Hogan, SC; Kacelnik, O; Parsons, CH; Rose, MM; King, AJ
      Auditory learning as a cause and treatment of central dysfunction

      AUDIOLOGY AND NEURO-OTOLOGY
    45. Fraenkel, R; Freeman, S; Sohmer, H
      The effect of various durations of noise exposure on auditory brainstem response, distortion product otoacoustic emissions and transient evoked otoacoustic emissions in rats

      AUDIOLOGY AND NEURO-OTOLOGY
    46. Wiley, JL; Bowen, SE; Balster, RL
      Effects of volatile inhalants on sensorimotor reactivity in rats

      ADDICTION BIOLOGY
    47. McBride, DI; Williams, S
      Audiometric notch as a sign of noise induced hearing loss

      OCCUPATIONAL AND ENVIRONMENTAL MEDICINE
    48. Ryan, AF; Keithley, EM; Harris, JP
      Autoimmune inner ear disorders

      CURRENT OPINION IN NEUROLOGY
    49. Flammer, J; Kaiser, H; Haufschild, T
      Susac syndrome: a vasospastic disorder?

      EUROPEAN JOURNAL OF OPHTHALMOLOGY
    50. Diaz, JH
      Epidemiology and outcome of postural headache management in spontaneous intracranial hypotension

      REGIONAL ANESTHESIA AND PAIN MEDICINE
    51. Stickler, GB; Hughes, W; Houchin, P
      Clinical features of hereditary progressive arthroophthalmopathy (Sticklersyndrome): A survey

      GENETICS IN MEDICINE
    52. Dong, JL; Katz, DR; Eng, CM; Kornreich, R; Desnick, RJ
      Nonradioactive detection. of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews

      MOLECULAR GENETICS AND METABOLISM
    53. Geller, AM; Oshiro, WM; Haykal-Coates, N; Kodavanti, PRS; Bushnell, PJ
      Gender-dependent behavioral and sensory effects of a commercial mixture ofpolychlorinated biphenyls (Aroclor 1254) in rats

      TOXICOLOGICAL SCIENCES
    54. Ritchie, GD; Still, KR; Alexander, WK; Nordholm, AF; Wilson, CL; Rossi, J; Mattie, DR
      A review of the neurotoxicity risk of selected hydrocarbon fuels

      JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART B-CRITICAL REVIEWS
    55. Vogler, C; Barker, J; Sands, MS; Levy, B; Galvin, N; Sly, WS
      Murine mucopolysaccharidosis VII: Impact of therapies on the phenotype, clinical course, and pathology in a model of a lysosomal storage disease

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    56. Hedrick, M; Younger, MS
      Perceptual weighting of relative amplitude and formant transition cues in aided CV syllables

      JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH
    57. Gordon-Salant, S; Fitzgibbons, PJ
      Sources of age-related recognition difficulty for time-compressed speech

      JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH
    58. Mackersie, CL; Prida, TL; Stiles, D
      The role of sequential stream segregation and frequency selectivity in theperception of simultaneous sentences by listeners with sensorineural hearing loss

      JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH
    59. Simsek, M; Al-Wardy, N; Al-Khabory, M
      A seminested PCR test for simultaneous detection of two common mutations (35delG and 167delT) in the connexin-26 gene

      MOLECULAR DIAGNOSIS
    60. Roizen, NJ
      Down syndrome: Progress in research

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    61. Pilotti, M; Beyer, T; Yasunami, M
      Encoding tasks and the processing of perceptual information in young and older adults

      JOURNALS OF GERONTOLOGY SERIES B-PSYCHOLOGICAL SCIENCES AND SOCIAL SCIENCES
    62. Lam, DK; Lawrence, HP; Tenenbaum, HC
      Aural symptoms in temporomandibular disorder patients attending a craniofacial pain unit

      JOURNAL OF OROFACIAL PAIN
    63. Lin, D; Goldstein, JA; Mhatre, AN; Lustig, LR; Pfister, M; Lalwani, AK
      Assessment of denaturing high-performance liquid chromatography (DHPLC) inscreening for mutations in connexin 26 (GJB2)

      HUMAN MUTATION
    64. Campbell, C; Cucci, RA; Prasad, S; Green, GE; Edeal, JB; Galer, CE; Karniski, LP; Sheffield, VC; Smith, RJH
      Pendred syndrome, DFNB4, and PDS/SCL26A4 identification of eight novel mutations and possible genotype-phenotype correlations

      HUMAN MUTATION
    65. Simdon, J; Watters, D; Bartlett, S; Connick, E
      Ototoxicity associated with use of nucleoside analog reverse transcriptaseinhibitors: A report of 3 possible cases and review of the literature

      CLINICAL INFECTIOUS DISEASES
    66. Price, DL; De Wilde, JP; Papadaki, AM; Curran, JS; Kitney, RI
      Investigation of acoustic noise on 15 MRI scanners from 0.2 T to 3 T

      JOURNAL OF MAGNETIC RESONANCE IMAGING
    67. Camargo, R; Limbert, E; Gillam, M; Henriques, MM; Fernandes, C; Catarino, AL; Soares, J; Alves, VAF; Kopp, P; Medeiros-Neto, G
      Aggressive metastatic follicular thyroid carcinoma with anaplastic transformation arising from a long-standing goiter in a patient with Pendred's syndrome

      THYROID
    68. Rahman, MU; Poe, DS; Choi, HK
      Autoimmune vestibulo-cochlear disorders

      CURRENT OPINION IN RHEUMATOLOGY
    69. Hsieh, RH; Li, JY; Pang, CY; Wei, YH
      A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy

      JOURNAL OF BIOMEDICAL SCIENCE
    70. Lambiris, AG; Newman, PL
      Marginal papular acrokeratodermas: No racial limitations for a clinical spectrum that responds to acitretin

      DERMATOLOGY
    71. Hutchin, TP; Navarro-Coy, NC; Van Camp, G; Tiranti, V; Zeviani, M; Schuelkes, M; Jaksch, M; Newton, V; Mueller, RF
      Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction

      EUROPEAN JOURNAL OF HUMAN GENETICS
    72. Loffler, J; Nekahm, D; Hirst-Stadlmann, A; Gunther, B; Menzel, HJ; Utermann, G; Janecke, AR
      Sensorineural hearing loss and the incidence of Cx26 mutations in Austria

      EUROPEAN JOURNAL OF HUMAN GENETICS
    73. Tessa, A; Giannotti, A; Tieri, L; Vilarinho, L; Marotta, G; Santorelli, FM
      Maternally inherited deafness associated with a T1095C mutation in the mDNA

      EUROPEAN JOURNAL OF HUMAN GENETICS
    74. Vanlieferinghen, P; Borderon, C; Francannet, C; Gembara, P; Dechelotte, P
      Johanson-Blizzard syndrome. A new case with autopsy findings

      GENETIC COUNSELING
    75. Daly, TM; Ohlemiller, KK; Roberts, MS; Vogler, CA; Sands, MS
      Prevention of systemic clinical disease in MPS VII mice following AAV-mediated neonatal gene transfer

      GENE THERAPY
    76. Peckham, C; Tookey, P; Logan, S; Giaquinto, C
      Screening options for prevention of congenital cytomegalovirus infection

      JOURNAL OF MEDICAL SCREENING
    77. Wayne, S; Robertson, NG; DeClau, F; Chen, N; Verhoeven, K; Prasad, S; Tranebjarg, L; Morton, CC; Ryan, AF; Van Camp, G; Smith, RJH
      Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus

      HUMAN MOLECULAR GENETICS
    78. Keeling, KM; Brooks, DA; Hopwood, JJ; Li, PN; Thompson, JN; Bedwell, DM
      Gentamicin-mediated suppression of Hurler syndrome stop mutations restoresa low level of alpha-L-iduronidase activity and reduces lysosomal glycosaminoglycan accumulation

      HUMAN MOLECULAR GENETICS
    79. Ng, L; Rusch, A; Amma, LL; Nordstrom, K; Erway, LC; Vennstrom, B; Forrest, D
      Suppression of the deafness and thyroid dysfunction in Thrb-null mice by an independent mutation in the Thra thyroid hormone receptor alpha gene

      HUMAN MOLECULAR GENETICS
    80. Robertson, NG; Resendes, BL; Lin, JS; Lee, C; Aster, JC; Adams, JC; Morton, CC
      Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9

      HUMAN MOLECULAR GENETICS
    81. Everett, LA; Belyantseva, IA; Noben-Trauth, K; Cantos, R; Chen, A; Thakkar, SI; Hoogstraten-Miller, SL; Kachar, B; Wu, DK; Green, ED
      Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome

      HUMAN MOLECULAR GENETICS
    82. Kelsell, DP; Dunlop, J; Hodgins, MB
      Human diseases: clues to cracking the connexin code?

      TRENDS IN CELL BIOLOGY
    83. Delb, W; Lipfert, S; Henn, W
      Mandibulofacial dysostosis, microcephaly and thorax deformities in two brothers: a new recessive syndrome?

      CLINICAL DYSMORPHOLOGY
    84. Ahmed, HO; Dennis, JH; Badran, O; Ismail, M; Ballal, SG; Ashoor, A; Jerwood, D
      High-frequency (10-18 kHz) hearing thresholds: reliability, and effects ofage and occupational noise exposure

      OCCUPATIONAL MEDICINE-OXFORD
    85. Mocci, F; Canalis, P; Tomasi, PA; Casu, F; Pettinato, S
      The effect of noise on serum and urinary magnesium and catecholamines in humans

      OCCUPATIONAL MEDICINE-OXFORD
    86. Karlsmose, B; Lauritzen, T; Engberg, M; Parving, A
      A randomised controlled trial of screening for adult hearing loss during preventive health checks

      BRITISH JOURNAL OF GENERAL PRACTICE
    87. Bedford, H; de Louvois, J; Halket, S; Peckham, C; Hurley, R; Harvey, D
      Meningitis in infancy in England and Wales: follow up at age 5 years

      BRITISH MEDICAL JOURNAL
    88. Hyodo, J; Hakuba, N; Koga, K; Watanabe, F; Shudou, M; Taniguchi, M; Gyo, K
      Hypothermia reduces glutamate efflux in perilymph following transient cochlear ischemia

      NEUROREPORT
    89. Ashmore, JF; Mammano, F
      Can you still see the cochlea for the molecules?

      CURRENT OPINION IN NEUROBIOLOGY
    90. Kaiser, A; Fedrowitz, M; Ebert, U; Zimmermann, E; Hedrich, HJ; Wedekind, D; Loscher, W
      Auditory and vestibular defects in the circling (ci2) rat mutant

      EUROPEAN JOURNAL OF NEUROSCIENCE
    91. Khalfa, S; Bruneau, N; Roge, B; Georgieff, N; Veuillet, E; Adrien, JL; Barthelemy, C; Collet, L
      Peripheral auditory asymmetry in infantile autism

      EUROPEAN JOURNAL OF NEUROSCIENCE
    92. Klemm, T; Neumann, S; Trulzsch, B; Pistrosch, F; Hanefeld, M; Paschke, R
      Search for mitochondrial DNA, mutation ate position 3243 in German patients with a positive family history of maternal diabetes mellitus

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    93. Fugazzola, L; Cerutti, N; Mannavola, D; Vannucchi, G; Beck-Peccoz, P
      The role of pendrin in iodide regulation

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    94. Gong, TWL; Besirli, CG; Lomax, MI
      MACF1 gene structure: a hybrid of plectin and dystrophin

      MAMMALIAN GENOME
    95. Cinamon, U; Bendet, E; Kronenberg, J
      Steroids, carbogen or placebo for sudden hearing loss: a prospective double-blind study

      EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
    96. Miani, C; Passon, P; Bracale, AMB; Barotti, A; Panzolli, N
      Treatment of hyperacusis in Williams syndrome with bilateral conductive hearing loss

      EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
    97. Burschka, MA; Hassan, HAH; Reineke, T; van Bebber, L; Caird, DM; Mosges, R
      Effect of treatment with Ginkgo biloba extract EGb 761 (oral) on unilateral idiopathic sudden hearing loss in a prospective randomized double-blind study of 106 outpatients

      EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
    98. Watanabe, K; Jinnouchi, K; Pawankar, R; Yagi, T
      Expression of myeloperoxidase and cochlear dysfunction in the lipopolysaccharide-treated guinea pig

      EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
    99. Herzog, M; Shehata-Dieler, WE; Dieler, R
      Transient evoked and distortion product otoacoustic emissions following successful stapes surgery

      EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
    100. Tashima, K; Uyama, E; Hashimoto, Y; Yonehara, T; Uchino, M
      Susac's syndrome: Beneficial effects of corticosteroid therapy in a Japanese case

      INTERNAL MEDICINE


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Documento generato il 01/11/20 alle ore 00:11:55