Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ronald Pennings"'
Autor:
Julie Moyaert, Annick Gilles, Griet Mertens, Marc J. W. Lammers, Hanne Gommeren, Sebastien Janssens de Varebeke, Erik Fransen, Nicolas Verhaert, Sam Denys, Raymond van de Berg, Ronald Pennings, Olivier Vanderveken, Vincent Van Rompaey
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Hearing impairment constitutes a significant health problem in developed countries. If hearing loss is slowly progressive, the first signs may not be noticed in time, or remain untreated until the moment the auditory dysfunction becomes more
Externí odkaz:
https://doaj.org/article/f23a352ba59845c0857dc714938806c7
Autor:
Laurence Jonard, Davide Brotto, Miguel A. Moreno-Pelayo, Ignacio del Castillo, Hannie Kremer, Ronald Pennings, Helena Caria, Graça Fialho, An Boudewyns, Guy Van Camp, Monika Ołdak, Dominika Oziębło, Naïma Deggouj, Romolo Daniele De Siati, Paolo Gasparini, Giorgia Girotto, Margriet Verstreken, Silvia Dossena, Sebastian Roesch, Saba Battelino, Katarina Trebušak Podkrajšek, Athanasia Warnecke, Thomas Lenarz, Anke Lesinski-Schiedat, Michel Mondain, Anne-Françoise Roux, Françoise Denoyelle, Natalie Loundon, Margaux Serey Gaut, Patrizia Trevisi, Elisa Rubinato, Alessandro Martini, Sandrine Marlin
Publikováno v:
Audiology Research, Vol 13, Iss 3, Pp 341-346 (2023)
The cause of childhood hearing impairment (excluding infectious pathology of the middle ear) can be extrinsic (embryofoetopathy, meningitis, trauma, drug ototoxicity, noise trauma, etc [...]
Externí odkaz:
https://doaj.org/article/1f272fa0e4ba4f1d9885851b72d3604b
Autor:
Vincent Van Rompaey, Hanne Gommeren, Joyce Bosmans, Dorien Verdoodt, Sebastien JanssensdeVarebeke, Erik de Vrieze, Ronald Pennings, Raymond Van de Berg, Marc Lammers, Olivier Vanderveken, Erik Fransen, Guy Van Camp, Erwin Van Wijk
Publikováno v:
B-ENT, Vol 18, Iss 4, Pp 273-283 (2022)
Externí odkaz:
https://doaj.org/article/2cb1c3d5a66a48399ec0d0f621b0140d
Autor:
Erik de Vrieze, Jorge Cañas Martín, Jolien Peijnenborg, Aniek Martens, Jaap Oostrik, Simone van den Heuvel, Kornelia Neveling, Ronald Pennings, Hannie Kremer, Erwin van Wijk
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 24, Iss , Pp 274-283 (2021)
The c.151C>T founder mutation in COCH is a frequent cause of late-onset, dominantly inherited hearing impairment and vestibular dysfunction (DFNA9) in the Dutch/Belgian population. The initial clinical symptoms only manifest between the 3rd and 5th d
Externí odkaz:
https://doaj.org/article/0da8c0567f494dd592518d218bfb3359
Publikováno v:
Genes; Volume 13; Issue 11; Pages: 1923
Genes, 13, 11
Genes, 13
Genes, 13, 11
Genes, 13
The relationship between speech recognition and hereditary hearing loss is not straightforward. Underlying genetic defects might determine an impaired cochlear processing of sound. We obtained data from nine groups of patients with a specific type of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aa761052336a568d5c7e107560aa2a2
Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by mutations inUSH2Aexon 13
Autor:
Ralph Slijkerman, Hester van Diepen, Silvia Albert, Margo Dona, Hanka Venselaar, Jingjing Zang, Stephan Neuhauss, Theo Peters, Sanne Broekman, Ronald Pennings, Hannie Kremer, Peter Adamson, Erik de Vrieze, Erwin van Wijk
Mutations inUSH2A, encoding usherin, are the most common cause of syndromic and non-syndromic retinitis pigmentosa (RP). The two founder mutations in exon 13 (c.2299delG and c.2276G>T) collectively account for~34% ofUSH2A-associated RP cases. Skippin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe2ad109fe6ef4c29d0127d47ec29d8b
https://doi.org/10.1101/2020.10.06.320499
https://doi.org/10.1101/2020.10.06.320499
Autor:
Erik de Vrieze, Jolien Peijnenborg, Jorge Cañas Martin, Aniek Martens, Jaap Oostrik, Simone van der Heuvel, Kornelia Neveling, Ronald Pennings, Hannie Kremer, Erwin van Wijk
The c.151C>T founder mutation in COCH is a frequent cause of late onset, dominantly inherited hearing impairment and vestibular dysfunction (DFNA9) in the Dutch/Belgian population. The initial clinical symptoms only manifest between the 3rd and 5th d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::312e92c3f8fa4bb34418b7ac134acb54
https://doi.org/10.1101/2020.09.29.316364
https://doi.org/10.1101/2020.09.29.316364
Autor:
Clark, Bartlett, Ronald, Pennings, Allan, Ho, David, Kirkpatrick, Rene, van Wijhe, Manohar, Bance
Publikováno v:
Journal of otolaryngology - headneck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale. 39(3)
Patulous eustachian tube (PET) has a major impact on a patient's quality of life. The purpose of this study was to understand mechanisms behind the symptoms, develop treatments based on these, and develop and use a questionnaire to measure changes in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c13054fffa2c7cd8782f149a8f657cf9
https://pubmed.ncbi.nlm.nih.gov/20470670
https://pubmed.ncbi.nlm.nih.gov/20470670