Some results of cochlear implants in 4 persons with usher's syndrome type I,

被引:0
|
作者
Vermeulen, L.
van Dijk, J.
Hinderink, H.
van den Broek, P.
机构
来源
| 1993年
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [31] Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I
    Zhou, Qi
    Lenger, Chaeli
    Smith, Richard
    Kimberling, William J.
    Ye, Ming
    Lehmann, Ordan
    MacDonald, Ian
    MOLECULAR VISION, 2012, 18 (142-45): : 1379 - 1383
  • [32] EVIDENCE FOR A 4TH LOCUS RESPONSIBLE FOR USHER-SYNDROME TYPE-I (USID)
    LARGETPIET, D
    GERBER, S
    ROZET, JM
    BONNEAU, D
    MATHIEU, M
    DERKALOUSTIAN, V
    MUNNICH, A
    KAPLAN, J
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 1885 - 1885
  • [33] CLINICAL FINDINGS IN OBLIGATE CARRIERS OF TYPE-I USHER SYNDROME
    WAGENAAR, M
    TERRAHE, B
    VANAAREM, A
    HUYGEN, P
    ADMIRAAL, R
    BLEEKERWAGEMAKERS, E
    PINCKERS, A
    KIMBERLING, W
    CREMERS, C
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 59 (03): : 375 - 379
  • [34] Pendular Nystagmus Presenting in Usher Syndrome Type I: A Case Report
    Bogle, Jamie M.
    Zapala, David A.
    JOURNAL OF THE AMERICAN ACADEMY OF AUDIOLOGY, 2024, 35 (09/10) : 263 - 269
  • [35] Living with type I Usher syndrome: insights from patients and their parents
    de Climens, Aude Roborel
    Tugaut, Beatrice
    Piscopo, Andrea
    Arnould, Benoit
    Buggage, Ronald
    Brun-Strang, Catherine
    OPHTHALMIC GENETICS, 2020, 41 (03) : 240 - 251
  • [36] Physical and psychological health, social trust, and financial situation for persons with Usher syndrome type 1
    Wahlqvist, Moa
    Moller, Kerstin
    Moller, Claes
    Danermark, Berth
    BRITISH JOURNAL OF VISUAL IMPAIRMENT, 2016, 34 (01) : 15 - 25
  • [37] Implications of Deafblindness: The Physical and Mental Health and Social Trust of Persons with Usher Syndrome Type 3
    Wahlqvist, Moa
    Moller, Claes
    Moller, Kerstin
    Danermark, Berth
    JOURNAL OF VISUAL IMPAIRMENT & BLINDNESS, 2016, 110 (04) : 245 - 256
  • [38] GENETIC-HETEROGENEITY OF USHER SYNDROME TYPE-I IN FRENCH FAMILIES
    KAPLAN, J
    GERBER, S
    BONNEAU, D
    LARGETPIET, D
    DOLLFUS, H
    ROZET, JM
    DUFIER, JL
    MUNNICH, A
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1993, 34 (04) : 1461 - 1461
  • [39] The characterisation and effect of myosin VIIa mutations in patients with Usher syndrome type I
    Payne, AM
    Upadhyaya, VJ
    Bessant, DAR
    Downes, SM
    Fitzke, FW
    Holder, GE
    Bird, AC
    Weston, MD
    Kimberling, WJ
    Bhattacharya, SS
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1997, 38 (04) : 3719 - 3719
  • [40] Usher Syndrome type I mutations in MYO7a and Harmonin.
    Weston, MD
    Astuto, LM
    Carney, CA
    Kimberling, WJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 647 - 647