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pro vyhledávání: '"Christopher P. Aldren"'
Autor:
Christopher P. Aldren
Publikováno v:
Scott-Brown's Essential Otorhinolaryngology ISBN: 9781003175995
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::085d39580a5470ea9fa6bc616a54eaec
https://doi.org/10.1201/9781003175995-12
https://doi.org/10.1201/9781003175995-12
Autor:
Robert Nash, Andrew J. Mowat, Jeremy Lavy, Barbara A. Cadge, Shakeel R. Saeed, Joanna L. Ziff, Michael Crompton, Sally J. Dawson, Christopher P. Aldren, Harry R. F. Powell
Publikováno v:
Otologyneurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 40(1)
Objective To analyse the epidemiology of otosclerosis in a British cohort collected between 2011 and 2017. Design Retrospective cohort study. Setting Five UK ENT Departments. Patients Patients with surgically confirmed otosclerosis. Main outcome meas
Autor:
Christopher P. Aldren, Thanos Bibas, Arnold J.N. Bittermann, George G. Browning, Wilko Grolman, Peter A. Rea, Rinze A. Tange, Inge Wegner
Publikováno v:
Scott-Brown’s Otorhinolaryngology Head and Neck Surgery ISBN: 9780203731017
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d351eb254aaf4ebb02142b2e2b73d300
https://doi.org/10.1201/9780203731017-89
https://doi.org/10.1201/9780203731017-89
Publikováno v:
Scott-Brown’s Otorhinolaryngology Head and Neck Surgery ISBN: 9780203731017
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4363121da01c4e64a95cfc49dd6f858
https://doi.org/10.1201/9780203731017-85
https://doi.org/10.1201/9780203731017-85
Autor:
Sally J. Dawson, Joanna L. Ziff, Christopher P. Aldren, Andrew J. Mowat, Jeremy Lavy, Michael Crompton, Shakeel R. Saeed
Publikováno v:
Human Genetics
Mowat, AJ, Crompton, M, Ziff, JL, Aldren, CP, Lavy, JA, Saeed, SR & Dawson, SJ 2018, ' Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population. ' Human Genetics . https://doi.org/10.1007/s00439-018-1889-9
Mowat, AJ, Crompton, M, Ziff, JL, Aldren, CP, Lavy, JA, Saeed, SR & Dawson, SJ 2018, ' Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population. ' Human Genetics . https://doi.org/10.1007/s00439-018-1889-9
Otosclerosis is a common form of hearing loss which typically presents in young adults. The disease has a familial, monogenic form and a non-familial form with a more complex aetiology. A previous genome wide association study identified evidence tha
Publikováno v:
British Journal of Audiology. 30:325-331
A new method of measuring the vestibulo-ocular reflex (VOR) during active head movements is presented. Subjects sat and attempted to maintain their gaze upon a fixed point whilst turning their heads from side to side in response to an auditory cue, t
Autor:
Shakeel R. Saeed, Harry R. F. Powell, Michael Crompton, Jeremy Lavy, Christopher P. Aldren, Sally J. Dawson, Karen P. Steel, Joanna L. Ziff
Publikováno v:
Human Molecular Genetics
Otosclerosis is a relatively common heterogenous condition, characterized by abnormal bone remodelling in the otic capsule leading to fixation of the stapedial footplate and an associated conductive hearing loss. Although familial linkage and candida