Zobrazeno 21 - 30
of 39
pro vyhledávání: '"Frederic Acke"'
Publikováno v:
Clinical Genetics. 89:416-425
Waardenburg syndrome (WS) is a rare genetic disorder characterized by hearing loss (HL) and pigment disturbances of hair, skin and iris. Classifications exist based on phenotype and genotype. The auditory phenotype is inconsistently reported among th
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 79:216-222
Objectives Etiological diagnosis of hearing impairment is of great importance to ensure early and adequate management. Even after thorough history taking, clinical and audiometric evaluation, the cause of hearing loss remains unclear in a majority of
Publikováno v:
Otology & Neurotology. 35:1196-1200
OBJECTIVE: Acquired atresia of the external auditory canal is a rare condition in which the medial part of the external auditory canal is obliterated by a soft fibrous plug, mostly as a result of chronic inflammation of the outer ear canal. In this s
Autor:
Pooja Takhar, Claus Bachert, G. Banfield, N. De Ruyck, Clare Harper, David J. Fear, Kayhan T. Nouri-Aria, Hannah J. Gould, H. H. Kariyawasam, Frederic Acke, Huifen Wu, Stephen R. Durham, Philippe Gevaert
Publikováno v:
Allergy. 68:55-63
BACKGROUND: Chronic rhinosinusitis with nasal polyps (NP) and allergic rhinitis (AR) is characterized by local Th2 inflammation and up-regulation of IgE; however, IgE in NP is ‘polyclonal’ and allergen specific, whereas IgE in AR is ‘oligoclona
Autor:
Guy Vingerhoets, Frederic Acke, Pieter Vandemaele, Jo Nys, Ann-Sofie Alderweireldt, Eric Achten
Publikováno v:
Hum Brain Mapp
We aimed to investigate the effect of hand effector and handedness on the cerebral lateralization of pantomiming learned movements. Fourteen right‐handed and 14 left‐handed volunteers performed unimanual and bimanual tool‐use pantomimes with th
Autor:
Fransiska Malfait, Frederic Acke, Olivier Vanakker, Paul Coucke, Anne De Paepe, Ingeborg Dhooge, Kim De Leeneer, Geert Mortier, Els De Leenheer, Wouter Steyaert
Publikováno v:
Molecular genetics and metabolism
Introduction: Stickler syndrome is caused by mutations in genes encoding type II and type XI collagens. About 85% of the pathogenic variants is found in COL2A1 (Stickler type 1), whereas a minority of mutations has been reported in COL11A1 (Stickler
Autor:
Stephan Vlaminck, Tom Vauterin, Peter Hellings, Mark Jorissen, Paul Van Cauwenberge, Frederic Acke, Claus Bachert, Philippe Gevaert
Publikováno v:
American journal of rhinology & allergy, 28(3), 260-264. OceanSide Publications Inc.
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BackgroundPatients with chronic rhinosinusitis with/without nasal polyps (CRSwNP/CRSsNP) benefit from endoscopic sinus surgery (ESS), with an estimated success rate of 80%. At present, the influence on clinical outcome after ESS of eosinophils, eosin
Autor:
Ingeborg Dhooge, Paul Van Cauwenberge, Frederic Acke, An De Sutter, Griet Vandeplas, Philippe Gevaert, Helen Van Hoecke, Olivier Thas
Publikováno v:
International archives of allergy and immunology. 163(2)
Background: Allergic rhinitis (AR) is a prevalent problem in general practice. The first evidence-based guidelines for AR, the ARIA guidelines, were published and have been updated repeatedly since 2001 in order to improve the care of AR patients. Ve
Publikováno v:
Acta neurologica Belgica. 111(4)
Autor:
Philippe Gevaert, Katrien Blomme, Hilde Lapeere, Peter Tomassen, Claus Bachert, Wouter Huvenne, Frederic Acke, Michiel Bonny
Publikováno v:
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
Background: Allergic rhinitis (AR) is the most common allergic disorder and its prevalence has significantly increased worldwide, nowadays affecting up to 40% of the population in young adults. The objective of the present survey was to evaluate the