Zobrazeno 1 - 10
of 32
pro vyhledávání: '"R. E. Quiney"'
Publikováno v:
BMJ Case Rep
A 36-year-old man presented with a 2-week history of a progressive forehead swelling and a frontal headache. He had no visual or neurological symptoms and there was no history of trauma. However, he reported a 4-week history of nasal obstruction with
Publikováno v:
The Journal of Laryngology & Otology. 128:73-77
Objective:To assess subjective preference using three nasal hygiene systems: Stérimar Original®, Emcur® and Sinus Rinse™.Design:We used a prospective, single-blind, randomised, crossover study to compare three nasal hygiene systems: Stérimar Or
Publikováno v:
The Journal of Laryngology & Otology. 124:583-586
Objectives:To review the current literature on the use of sodium fluoride in the treatment of otosclerosis.Design:A literature review was conducted, searching the Medline and PubMed database from 1966 to 2009, using the terms ‘otosclerosis’ and
Publikováno v:
Acta Paediatrica. 92:28-30
Aim: To describe the nature and prevalence of hearing loss in Fabry disease, and its response to enzyme replacement therapy (ERT) with agalsidase alfa. Methods: Fifteen male patients with Fabry disease were enrolled in a randomized, double-blind stud
Publikováno v:
The Journal of Laryngology & Otology. 110:567-569
A Case Is reported of a 59-year-old Caucasian male with oculopharyngeal myopathy and sensorineural hearing loss. He presented with progressive ptosis, sensorineural hearing loss over several years and symptoms of mild dysphagia. Further enquiry into
Publikováno v:
Journal of inherited metabolic disease. 26(8)
The aim of this study was to describe the nature and prevalence of hearing loss in Fabry disease (McKusick 301500), a rare X-linked lysosomal storage disorder, and its response to enzyme replacement therapy with agalsidase alfa. Fifteen hemizygous ma
Publikováno v:
The Journal of laryngology and otology. 113(12)
Langerhans' cell histiocytosis is a rare disorder of unknown aetiology in which pathological Langerhans' cells accumulate and destroy local tissue. We report a 38-year-old female who presented with a sudden onset of left sensormeural hearing loss. Ma
Publikováno v:
The Journal of infection. 34(2)
As the prevalence of tuberculosis in the U.K. increases, uncommon clinical presentations of the disease may be encountered by the otolaryngologist. We describe just such a case, where a caucasian patient presented with laryngeal lesion, considered to
Publikováno v:
The Journal of laryngology and otology. 105(4)
The presence of human papillomavirus (HPV) genomes 6, 11, 16 and 33 in 16 patients with laryngopharyngeal carcinomas was examined by means of a polymerase chain reaction. HPV genomes were detected in 75 per cent of cases. In hypopharyngeal carcinoma,
Autor:
R E, Quiney, L, Michaels
Publikováno v:
The Journal of otolaryngology. 19(4)
The detailed postmortem laryngeal findings of a man with an established vocal cord palsy from an inoperable bronchial carcinoma is presented. Fine dissection of the monoblock specimen from skull base to superior mediastinum allowed sampling of vagus,