Lack of ciprofloxacin ototoxicity after repeated ototopical application.

Por Claes, J, Govaerts, P J, Van de Heyning, P H, Peeters, S
Publicado em 1991

Two months follow up of auto-CPAP treatment in patients with obstructive sleep apnoea

Por Boudewyns, A, Grillier-Lanoir, V, Willemen, M, De Cock, W A, Van de Heyning, P H, De Backer, W A
Publicado em 1999

Effect of isepamicin dosing scheme on concentration in cochlear tissue.

Por Govaerts, P J, Claes, J, Van de Heyning, P H, Derde, M P, Kaufman, L, Marquet, J F, De Broe, M E
Publicado em 1991

Treatment of obstructive sleep apnea using a custom-made titratable duobloc oral appliance: a prospective clinical study

Por Dieltjens, M., Vanderveken, O. M., Hamans, E., Verbraecken, J. A., Wouters, K., Willemen, M., De Backer, W. A., Van de Heyning, P. H., Braem, M. J.
Publicado em 2012

Mal de Debarquement Syndrome: a survey on subtypes, misdiagnoses, onset and associated psychological features

Por Mucci, V., Canceri, J. M., Brown, R., Dai, M., Yakushin, S., Watson, S., Van Ombergen, A., Topsakal, V., Van de Heyning, P. H., Wuyts, F. L., Browne, C. J.
Publicado no J Neurol (2018)

A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus

Por Van Camp, G., Kunst, H., Flothmann, K., McGuirt, W., Wauters, J., Marres, H., Verstreken, M., Bespalova, I., Burmeister, M., Van de Heyning, P. H, Smith, R., Willems, P., Cremers, C., Lesperance, M.
Publicado em 1999

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Por Verhoeven, K, Van Camp, G, Govaerts, P J, Balemans, W, Schatteman, I, Verstreken, M, Van Laer, L, Smith, R J, Brown, M R, Van de Heyning, P H, Somers, T, Offeciers, F E, Willems, P J
Publicado em 1997

A genotype-phenotype correlation for GJB2 (connexin 26) deafness

Por Cryns, K, Orzan, E, Murgia, A, Huygen, P, Moreno, F, del Castillo, I, Parker, C, Azaiez, H, Prasad, S, Cucci, R, Leonardi, E, Snoeckx, R, Govaerts, P, Van de Heyning, P H, Van de Heyning, C M, Smith, R, Van Camp, G
Publicado em 2004

A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation

Por FRANSEN, E., VERSTREKEN, M., BOM, S., LEMAIRE, F., KEMPERMAN, M., DE KOK, Y. J M, WUYTS, F., VERHAGEN, W., HUYGEN, P., MCGUIRT, W., SMITH, R., VAN MALDERGEM, L., DECLAU, F., CREMERS, C., VAN DE HEYNING, P. H, CREMERS, F., VAN CAMP, G.
Publicado em 2001