Fransen E - Search Results

1

Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9).

Verhagen WI, Bom SJ, Huygen PL, Fransen E, Van Camp G, Cremers CW. Verhagen WI, et al. Among authors: fransen e. Arch Neurol. 2000 Jul;57(7):1045-7. doi: 10.1001/archneur.57.7.1045. Arch Neurol. 2000. PMID: 10891988

2

L1-associated diseases: clinical geneticists divide, molecular geneticists unite.

Fransen E, Van Camp G, Vits L, Willems PJ. Fransen E, et al. Hum Mol Genet. 1997;6(10):1625-32. doi: 10.1093/hmg/6.10.1625. Hum Mol Genet. 1997. PMID: 9300653 Review.

3

Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expression.

Verhagen WI, Bartels RH, Fransen E, van Camp G, Renier WO, Grotenhuis JA. Verhagen WI, et al. Among authors: fransen e. J Neurol Sci. 1998 Jun 11;158(1):101-5. doi: 10.1016/s0022-510x(98)00097-5. J Neurol Sci. 1998. PMID: 9667786 Review.

4

Dependence of the ligation efficiency of large DNA fragments isolated from agarose gels on the purification method.

Fransen E, Van Camp G, Winnepenninckx B. Fransen E, et al. Prep Biochem Biotechnol. 1998 Aug;28(3):235-41. doi: 10.1080/10826069808010138. Prep Biochem Biotechnol. 1998. PMID: 9710896

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. Hum Mol Genet. 1999 Aug;8(8):1425-9. doi: 10.1093/hmg/8.8.1425. Hum Mol Genet. 1999. PMID: 10400989

6

The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?

Fransen E, Van Camp G. Fransen E, et al. Br J Audiol. 1999 Oct;33(5):297-302. doi: 10.3109/03005369909090113. Br J Audiol. 1999. PMID: 10890144

7

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

Fransen E, Verstreken M, Bom SJ, Lemaire F, Kemperman MH, De Kok YJ, Wuyts FL, Verhagen WI, Huygen PL, McGuirt WT, Smith RJ, Van Maldergem LV, Declau F, Cremers CW, Van De Heyning PH, Cremers FP, Van Camp G. Fransen E, et al. J Med Genet. 2001 Jan;38(1):61-5. doi: 10.1136/jmg.38.1.61. J Med Genet. 2001. PMID: 11332404 Free PMC article. No abstract available.

8

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.

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 RJ, Van Camp G. Van Laer L, et al. Among authors: fransen e. J Med Genet. 2001 Aug;38(8):515-8. doi: 10.1136/jmg.38.8.515. J Med Genet. 2001. PMID: 11483639 Free PMC article.

9

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: fransen e. Otol Neurotol. 2001 Nov;22(6):874-81. doi: 10.1097/00129492-200111000-00028. Otol Neurotol. 2001. PMID: 11698812

10

Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a family.

Verhagen WI, Bom SJ, Fransen E, Van Camp G, Huygen PL, Theunissen EJ, Cremers CW. Verhagen WI, et al. Among authors: fransen e. Clin Otolaryngol Allied Sci. 2001 Dec;26(6):477-83. doi: 10.1046/j.1365-2273.2001.00505.x. Clin Otolaryngol Allied Sci. 2001. PMID: 11843927

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