Declau F - Search Results

1

Three Years of Vestibular Infant Screening in Infants With Sensorineural Hearing Loss.

Martens S, Dhooge I, Dhondt C, Vanaudenaerde S, Sucaet M, Van Hoecke H, De Leenheer E, Rombaut L, Boudewyns A, Desloovere C, Vinck AS, de Varebeke SJ, Verschueren D, Verstreken M, Foulon I, Staelens C, De Valck C, Calcoen R, Lemkens N, Öz O, De Bock M, Haverbeke L, Verhoye C, Declau F, Devroede B, Forton G, Deggouj N, Maes L. Martens S, et al. Among authors: declau f. Pediatrics. 2022 Jul 1;150(1):e2021055340. doi: 10.1542/peds.2021-055340. Pediatrics. 2022. PMID: 35698886

2

Differentiation of cartilage and bone in human fetal temporal bones with Luxol fast blue stain.

Declau F, Moeneclaey L, Forton G, Marquet J. Declau F, et al. Arch Otorhinolaryngol. 1988;245(4):218-20. doi: 10.1007/BF00463930. Arch Otorhinolaryngol. 1988. PMID: 2460074

3

The involvement of the cochlear nerve in neurinomas of the eighth cranial nerve.

Forton G, Moeneclaey L, Declau F, Marquet J. Forton G, et al. Among authors: declau f. Arch Otorhinolaryngol. 1989;246(3):156-60. doi: 10.1007/BF00456658. Arch Otorhinolaryngol. 1989. PMID: 2474289

4

Subcutaneous diffuse neurofibroma of the neck: a case report.

de Varebeke SJ, De Schepper A, Hauben E, Declau F, Van Marck E, Van de Heyning PH. de Varebeke SJ, et al. Among authors: declau f. J Laryngol Otol. 1996 Feb;110(2):182-4. doi: 10.1017/s0022215100133122. J Laryngol Otol. 1996. PMID: 8729511

5

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

Fransen E, Verstreken M, Verhagen WI, Wuyts FL, Huygen PL, D'Haese P, Robertson NG, Morton CC, McGuirt WT, Smith RJ, Declau F, Van de Heyning PH, Van Camp G. Fransen E, et al. Among authors: declau f. Hum Mol Genet. 1999 Aug;8(8):1425-9. doi: 10.1093/hmg/8.8.1425. Hum Mol Genet. 1999. PMID: 10400989

6

Audiometric analysis of a Belgian family linked to the DFNA10 locus.

Verstreken M, Declau F, Schatteman I, Van Velzen D, Verhoeven K, Van Camp G, Willems PJ, Kuhweide EW, Verhaert E, D'Haese P, Wuyts FL, Van de Heyning PH. Verstreken M, et al. Among authors: declau f. Am J Otol. 2000 Sep;21(5):675-81. Am J Otol. 2000. PMID: 10993457

7

Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH gene.

Verstreken M, Declau F, Wuyts FL, D'Haese P, Van Camp G, Fransen E, Van den Hauwe L, Buyle S, Smets RE, Feenstra L, Van der Stappen A, Van de Heyning PH. Verstreken M, et al. Among authors: declau f. Otol Neurotol. 2001 Nov;22(6):874-81. doi: 10.1097/00129492-200111000-00028. Otol Neurotol. 2001. PMID: 11698812

8

Otosclerosis: a genetically heterogeneous disease involving at least three different genes.

Van Den Bogaert K, Govaerts PJ, De Leenheer EM, Schatteman I, Verstreken M, Chen W, Declau F, Cremers CW, Van De Heyning PH, Offeciers FE, Somers T, Smith RJ, Van Camp G. Van Den Bogaert K, et al. Among authors: declau f. Bone. 2002 Apr;30(4):624-30. doi: 10.1016/s8756-3282(02)00679-8. Bone. 2002. PMID: 11934656

9

DFNA10/EYA4--the clinical picture.

De Leenheer EM, Huygen PL, Wayne S, Verstreken M, Declau F, Van Camp G, Van de Heyning PH, Smith RJ, Cremers CW. De Leenheer EM, et al. Among authors: declau f. Adv Otorhinolaryngol. 2002;61:73-8. doi: 10.1159/000066807. Adv Otorhinolaryngol. 2002. PMID: 12408066 No abstract available.

10

Universal newborn hearing screening.

Declau F, Doyen A, Robillard T, de Varebeke SJ. Declau F, et al. B-ENT. 2005;Suppl 1:16-21; quiz 22-3. B-ENT. 2005. PMID: 16363265

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