Zobrazeno 1 - 10
of 45
pro vyhledávání: '"R.J.H. Ensink"'
Publikováno v:
Otorinolaringologia. 68
Autor:
R.J.H. Ensink, Farrel J. Buchinsky, Abebe Melaku, Alden F. Smith, Margaretha L. Casselbrant, David C. Ianacone, Glenn Isaacson
Publikováno v:
International journal of pediatric otorhinolaryngology. 103
To determine the prevalence of chronic ear disease in HIV+, highly active anti-retroviral therapy (HAART)-treated children and compare this to the prevalence in healthy children of similar age living in a similar setting.From previous clinical work i
Publikováno v:
International Journal of Pediatric Otorhinolaryngology, 78, 1179-81
International Journal of Pediatric Otorhinolaryngology, 78, 7, pp. 1179-81
International Journal of Pediatric Otorhinolaryngology, 78, 7, pp. 1179-81
Item does not contain fulltext We report on a new-born with a congenital mucocele on the anterior dorsal side of the tongue. The presentation as well as the differential diagnosis of congenital oral swellings is discussed. Because of breastfeeding pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a62a5d1ad7f957efef37d459040c565c
https://doi.org/10.1016/j.ijporl.2014.04.012
https://doi.org/10.1016/j.ijporl.2014.04.012
Autor:
E.M.R. De Leenheer, Martijn H. Kemperman, C.W.R.J. Cremers, G. Van Camp, F. P. M. Cremers, Arjan J. Bosman, Henri A. M. Marres, Francois X Lemaire, R.J.H. Ensink, Steven J. H. Bom, Patrick L. M. Huygen, Wim I. M. Verhagen, Henricus P. M. Kunst
Publikováno v:
Archives of otolaryngology, head and neck surgery
Archives of Otolaryngology--Head & Neck Surgery, 127, 1045-8
Archives of Otolaryngology--Head & Neck Surgery, 127, 9, pp. 1045-8
Archives of Otolaryngology--Head & Neck Surgery, 127, 1045-8
Archives of Otolaryngology--Head & Neck Surgery, 127, 9, pp. 1045-8
Item does not contain fulltext OBJECTIVE: To analyze the relationship between pure-tone hearing threshold and speech recognition performance in DFNA2/KCNQ4 and DFNA9/COCH, 2 types of high-frequency nonsyndromic hearing impairment. DESIGN: Case series
Autor:
Paul Coucke, Patrick L. M. Huygen, P. van Hauwe, R.J.H. Ensink, C.W.R.J. Cremers, G. Van Camp
Publikováno v:
European Archives of Oto-Rhino-Laryngology, 257, 62-67
European archives of oto-rhino-laryngology
European Archives of Oto-Rhino-Laryngology, 257, pp. 62-67
European archives of oto-rhino-laryngology
European Archives of Oto-Rhino-Laryngology, 257, pp. 62-67
We studied a Dutch family with DFNA2-linked progressive sensorineural hearing impairment (SNHI). Recent audiograms were obtained from 18 of the affected persons (age 7-81 years) and were used in a gene-linkage analysis. Linear regression analysis of
Autor:
G. Van Camp, Paul Coucke, P. van Hauwe, R.J.H. Ensink, Patrick L. M. Huygen, C.W.R.J. Cremers
Publikováno v:
American Journal of Medical Genetics, 93, 184-187
American Journal of Medical Genetics, 93, 3, pp. 184-187
American journal of medical genetics
American Journal of Medical Genetics, 93, 3, pp. 184-187
American journal of medical genetics
The DFNA2 locus for autosomal dominant nonsyndromic hearing impairment on chromosome 1p34 contains at least 2 genes responsible for hearing loss, GJB3 and KCNQ4. GJB3 is a member of the connexin gene family and KCNQ4 is a voltage-gated potassium chan
Autor:
R.J.H. Ensink, B.J.M. de Swart, S. Knuijt, B.G.M. van Engelen, J.A. van der Vliet, A.A. Tieleman
Publikováno v:
Neuromuscular Disorders, 19, 196-8
Neuromuscular Disorders, 19, 3, pp. 196-8
Neuromuscular Disorders, 19, 196-198
Neuromuscular Disorders, 19, 3, pp. 196-8
Neuromuscular Disorders, 19, 196-198
Contains fulltext : 80874.pdf (Publisher’s version ) (Closed access) The phenotype of myotonic dystrophy type 2 (DM2) shows similarities as well as differences to that of myotonic dystrophy type 1 (DM1). Dysphagia, a predominant feature in DM1, has
Publikováno v:
Clinical Otolaryngology, 23, 3-8
Clinical otolaryngology & allied sciences
Clinical Otolaryngology, 23, pp. 3-8
Clinical otolaryngology & allied sciences
Clinical Otolaryngology, 23, pp. 3-8
Item does not contain fulltext
Publikováno v:
International Journal of Pediatric Otorhinolaryngology
International Journal of Pediatric Otorhinolaryngology, 38, pp. 237-245
International Journal of Pediatric Otorhinolaryngology, 237-245
STARTPAGE=237;ENDPAGE=245;ISSN=0165-5876;TITLE=International Journal of Pediatric Otorhinolaryngology
International Journal of Pediatric Otorhinolaryngology, 38, pp. 237-245
International Journal of Pediatric Otorhinolaryngology, 237-245
STARTPAGE=237;ENDPAGE=245;ISSN=0165-5876;TITLE=International Journal of Pediatric Otorhinolaryngology
Sensorineural hearing loss affects approximately 1 in 2 persons at about 80 years of age and 1 in 750 in childhood. The best known forms of hearing loss with an autosomal dominant pattern of inheritance are the syndromic-mediated ones. At present, th
Publikováno v:
The Journal of Laryngology & Otology. 110:952-957
A three-generation family with Saethre-Chotzen syndrome and an isolated case are presented. The proband presented with conductive hearing loss. His mother and grandmother showed minor features of the syndrome including conductive hearing loss.Symptom