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Results: 1-13 |
Results: 13
Hereditary otovestibular dysfunction and Meniere's disease in a large Belgian family is caused by a missense mutation in the COCH gene
Authors: Verstreken, M Declau, F Wuyts, FL D'Haese, P Van Camp, G Fransen, E Van den Hauwe, L Buyle, S Smets, REM Feenstra, L Van der Stappen, A Van de Heyning, PH
Citation: M. Verstreken et al., Hereditary otovestibular dysfunction and Meniere's disease in a large Belgian family is caused by a missense mutation in the COCH gene, OTOL NEURO, 22(6), 2001, pp. 874-881
Entorhinal neuronal activity during delayed matching tasks may depend uponmuscarinic-induced non-specific cation current I(CANM)
Authors: Fransen, E Alonso, AA Hasselmo, ME
Citation: E. Fransen et al., Entorhinal neuronal activity during delayed matching tasks may depend uponmuscarinic-induced non-specific cation current I(CANM), NEUROCOMPUT, 38, 2001, pp. 601-606
A common founder for the 35deIG GJB2 gene mutation in connexin 26 hearing impairment
Authors: Van Laer, L Coucke, P Mueller, RF Caethoven, G Flothmann, K Prasad, SD Chamberlin, GP Houseman, M Taylor, GR Van de Heyning, CM Fransen, E Rowland, J Cucci, RA Smith, RJH Van Camp, G
Citation: L. Van Laer et al., A common founder for the 35deIG GJB2 gene mutation in connexin 26 hearing impairment, J MED GENET, 38(8), 2001, pp. 515-518
A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation
Authors: Fransen, E Verstreken, M Bom, SJH Lemaire, F Kemperman, MH De Kok, YJM Wuyts, FL Verhagen, WIM Huygen, PLM McGuirt, WT Smith, RJH Van Maldergem, L Declau, F Cremers, CWRJ Van de Heyning, PH Cremers, FPM Van Camp, G
Citation: E. Fransen et al., A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation, J MED GENET, 38(1), 2001, pp. 61-64
Long-term potentiation in mice lacking the neural cell adhesion molecule L1
Authors: Bliss, T Errington, M Fransen, E Godfraind, JM Kauer, JA Kooy, RF Maness, PF Furley, AJW
Citation: T. Bliss et al., Long-term potentiation in mice lacking the neural cell adhesion molecule L1, CURR BIOL, 10(24), 2000, pp. 1607-1610
Properties and role of I-h in the pacing of subthreshold oscillations in entorhinal cortex layer II neurons
Authors: Dickson, CT Magistretti, J Shalinsky, MH Fransen, E Hasselmo, ME Alonso, A
Citation: Ct. Dickson et al., Properties and role of I-h in the pacing of subthreshold oscillations in entorhinal cortex layer II neurons, J NEUROPHYS, 83(5), 2000, pp. 2562-2579
Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9)
Authors: Verhagen, WIM Bom, SJH Huygen, PLM Fransen, E Van Camp, G Cremers, CWRJ
Citation: Wim. Verhagen et al., Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9), ARCH NEUROL, 57(7), 2000, pp. 1045-1047
Patterns of p53 gene mutations in head and neck cancer: Full-length gene sequencing and results of primary radiotherapy
Authors: Saunders, ME MacKenzie, R Shipman, R Fransen, E Gilbert, R Jordan, RCK
Citation: Me. Saunders et al., Patterns of p53 gene mutations in head and neck cancer: Full-length gene sequencing and results of primary radiotherapy, CLIN CANC R, 5(9), 1999, pp. 2455-2463
High prevalence of symptoms of Meniere's disease in three families with a mutation in the COCH gene
Authors: Fransen, E Verstreken, M Verhagen, WIM Wuyts, FL Huygen, PLM D'Haese, P Robertson, NG Morton, CC McGuirt, WT Smith, RJH Declau, F Van de Heyning, PH Van Camp, G
Citation: E. Fransen et al., High prevalence of symptoms of Meniere's disease in three families with a mutation in the COCH gene, HUM MOL GEN, 8(8), 1999, pp. 1425-1429
A biophysical simulation of intrinsic and network properties of entorhinalcortex
Authors: Fransen, E Wallenstein, GV Alonso, AA Dickson, CT Hasselmo, ME
Citation: E. Fransen et al., A biophysical simulation of intrinsic and network properties of entorhinalcortex, NEUROCOMPUT, 26-7, 1999, pp. 375-380
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
Authors: Fransen, E Van Camp, G
Citation: E. Fransen et G. Van Camp, The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?, BR J AUDIOL, 33(5), 1999, pp. 297-302
Impact of blood transfusions on inflammatory mediator release in patients undergoing cardiac surgery
Authors: Fransen, E Maessen, J Dentener, M Senden, N Buurman, W
Citation: E. Fransen et al., Impact of blood transfusions on inflammatory mediator release in patients undergoing cardiac surgery, CHEST, 116(5), 1999, pp. 1233-1239
A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11
Authors: Reyniers, E Van Bogaert, P Peeters, N Vits, L Pauly, F Fransen, E Van Regemorter, N Kooy, RF
Citation: E. Reyniers et al., A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11, AM J HU GEN, 65(5), 1999, pp. 1406-1412
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