Modelling Hebbian cell assemblies comprised of cortical neuronsLANSNER, A; FRANSEN, E.Network (Bristol. Print). 1992, Vol 3, Num 2, pp 105-119, issn 0954-898XArticle

Overtraining following intensified training with normal muscle glycogenSNYDER, A. C; KUIPERS, H; BO CHENG et al.Medicine and science in sports and exercise. 1995, Vol 27, Num 7, pp 1063-1070, issn 0195-9131Article

Parsing the components of the psychomotor syndrome in schizophreniaDOCX, L; MORRENS, M; BERVOETS, C et al.Acta psychiatrica scandinavica. 2012, Vol 126, Num 4, pp 256-265, issn 0001-690X, 10 p.Article

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairmentVAN LAER, L; COUCKE, P; FRANSEN, E et al.Journal of medical genetics. 2001, Vol 38, Num 8, pp 515-518, issn 0022-2593Article

A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11REYNIERS, E; VAN BOGAERT, P; PEETERS, N et al.American journal of human genetics. 1999, Vol 65, Num 5, pp 1406-1412, issn 0002-9297Article

Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH geneVERSTREKEN, M; DECLAU, F; VAN DER STAPPEN, A et al.Otology & neurotology. 2001, Vol 22, Num 6, pp 874-881, issn 1531-7129Article

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH geneFRANSEN, E; VERSTREKEN, M; DECLAU, F et al.Human molecular genetics (Print). 1999, Vol 8, Num 8, pp 1425-1429, issn 0964-6906Article

The COCH gene : a frequent cause of hearing impairment and vestibular dysfunction?FRANSEN, E; VAN CAMP, G.British journal of audiology. 1999, Vol 33, Num 5, pp 297-302, issn 0300-5364Conference Paper

MRI as a tool to study brain structure in mouse models for mental retardationVERHOYE, M; SIJBERS, J; KOOY, R. F et al.SPIE proceedings series. 1998, Vol 3337, pp 314-320, isbn 0-8194-2782-9Conference Paper

X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM geneFRANSEN, E; SCHRANDER-STUMPEL, C; VITS, L et al.Human molecular genetics (Print). 1994, Vol 3, Num 12, pp 2255-2256, issn 0964-6906Article

Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentVAN EYKEN, E; VAN CAMP, G; JENSEN, M et al.Journal of medical genetics. 2007, Vol 44, Num 9, pp 570-578, issn 0022-2593, 9 p.Article

Patterns of p53 gene mutations in head and neck cancer : Full-length gene sequencing and results of primary radiotherapySAUNDERS, M. E; MACKENZIE, R; SHIPMAN, R et al.Clinical cancer research. 1999, Vol 5, Num 9, pp 2455-2463, issn 1078-0432Article

Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expressionVERHAGEN, W. I. M; BARTELS, R. H. A. M; FRANSEN, E et al.Journal of the neurological sciences. 1998, Vol 158, Num 1, pp 101-105, issn 0022-510XArticle

L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patternsFRANSEN, E; D'HOOGE, R; DE ZEEUW, C. I et al.Human molecular genetics (Print). 1998, Vol 7, Num 6, pp 999-1009, issn 0964-6906Article

Release of lipopolysaccharide toxicity-modulating proteins in patients undergoing cardiopulmonary bypass using noncoated and heparin-coated extracorporeal circuits : A clinical pilot studyBOUMA, M; MAESSEN, J; WEERWIND, P et al.Chest. 1997, Vol 111, Num 3, pp 577-583, issn 0012-3692Article

Psychosocial problems associated with depression at 18 months poststrokeDE RYCK, A; FRANSEN, E; BROUNS, R et al.International journal of geriatric psychiatry. 2014, Vol 29, Num 2, pp 144-152, issn 0885-6230, 9 p.Article

Impact of Blood transfusions on inflammatory mediator release in patients undergoing cardiac surgeryFRANSEN, E; MAESSEN, J; DENTENER, M et al.Chest. 1999, Vol 116, Num 5, pp 1233-1239, issn 0012-3692Article

Genotype-phenotype correlation in L1 associated diseasesFRANSEN, E; VAN CAMP, G; D'HOOGE, R et al.Journal of medical genetics. 1998, Vol 35, Num 5, pp 399-404, issn 0022-2593Article

Systemic inflammation present in patients undergoing CABG without extracorporeal circulationFRANSEN, E; MAESSEN, J; DENTENER, M et al.Chest. 1998, Vol 113, Num 5, pp 1290-1295, issn 0012-3692Article

L1-associated diseases : clinical geneticists divide, molecular geneticists uniteFRANSEN, E; VAN CAMP, G; VITS, L et al.Human molecular genetics (Print). 1997, Vol 6, Num 10, pp 1625-1632, issn 0964-6906Article

Positional cloning of a gene involved in hereditary multiple exostosesWUYTS, W; VAN HUL, M; BOSSUYT, P et al.Human molecular genetics (Print). 1996, Vol 5, Num 10, pp 1547-1557, issn 0964-6906Article

BMI-related metabolic composition of the follicular fluid of women undergoing assisted reproductive treatment and the consequences for oocyte and embryo qualityVALCKX, S. D. M; DE PAUW, I; DE NEUBOURG, D et al.Human reproduction (Oxford. Print). 2012, Vol 27, Num 12, pp 3531-3539, issn 0268-1161, 9 p.Article

Einfluss exogener Faktoren auf Altersschwerhörigkeit = Influence of exogenic factors on age-related hearing impairmentBAUR, M; FRANSEN, E; TROPITZSCH, A et al.HNO. Hals-, Nasen-, Ohrenärzte. 2009, Vol 57, Num 10, pp 1023-1028, issn 0017-6192, 6 p.Article

Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9)VERHAGEN, W. I. M; BOM, S. J. H; HUYGEN, P. L. M et al.Archives of neurology (Chicago). 2000, Vol 57, Num 7, pp 1045-1047, issn 0003-9942Article

The clinical spectrum of mutations in L1, a neuronal cell adhesion moleculeFRANSEN, E; VITS, L; VAN CAMP, G et al.American journal of medical genetics. 1996, Vol 64, Num 1, pp 73-77, issn 0148-7299Article