Zobrazeno 1 - 10
of 52
pro vyhledávání: '"T. Van Dyck"'
Autor:
T Van Dyck, R. Van den Broeck, R Cornelissen, Ilse Smets, P Ockier, Jan Dries, M Feyaerts, S.W.H. Van Hulle
Publikováno v:
Water science and technology
A survey regarding online instrumentation and control was conducted among 90 companies managing their own biological wastewater treatment plant in Flanders, Belgium. In this study, all types of online instrumentation have been found suitable for auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa99233d607e850765c527649cdd5adb
https://doi.org/10.2166/wst.2018.375
https://doi.org/10.2166/wst.2018.375
Voxelwise harmonisation of FA on a cohort of 605 healthy subjects using ComBat: an exploratory study
Publikováno v:
ESMRMB 2019, 36th Annual Scientific Meeting, Rotterdam, The Netherlands, Magn Reson Mater Phy, 2019
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=r3c4b2081b22::951cc23beaa650fe0b77f5eacffcf153
Autor:
Ivo F.J. Vankelecom, T. Van Dyck, C. Van Goethem, Matthias Mertens, Abaynesh Yihdego Gebreyohannes
© 2018 Elsevier B.V. Integrally skinned asymmetric nanofiltration (NF) membranes are widely used for treating a variety of aqueous and solvent streams. Polyvinylidene difluoride (PVDF), is an excellent film forming polymer with outstanding chemical,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c76efa1573cb9d90e16c9c2e647da4b
https://lirias.kuleuven.be/handle/123456789/624706
https://lirias.kuleuven.be/handle/123456789/624706
Autor:
Thijs Defraeye, Pieter Verboven, Johan Claes, Martine Wevers, Els Herremans, T. Van Dyck, Bart Nicolai, L. Van Campenhout
Publikováno v:
Journal of Food Engineering. 123:67-77
X-ray micro-tomography and a volume stitching strategy were combined to create a high resolution 3D image of entire cross sections (slices) of bread. Morphological analysis of whole slices revealed structural properties on a product scale. The additi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fce3556d36313c6ea4081c10928efe48
https://doi.org/10.1016/j.jfoodeng.2013.09.017
https://doi.org/10.1016/j.jfoodeng.2013.09.017
Autor:
Samuel F. Berkovic, Philip Holmgren, Dirk Goossens, Jurgen Del-Favero, T Van Dyck, Berten Ceulemans, Kristien Verhaert, Lieven Lagae, Ingrid E. Scheffer, Albena Jordanova, Anna Jansen, Arvid Suls, Liesbet Deprez, P. De Jonghe, Simone C. Yendle, R. Van Coster, Sarah Weckhuysen
Publikováno v:
Neurology
ResearcherID
ResearcherID
Objectives: Heterozygous mutations in STXBP1, encoding the syntaxin binding protein 1, have recently been identified in Ohtahara syndrome, an epileptic encephalopathy with very early onset. In order to explore the phenotypic spectrum associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12d1d8d514bc8605e6877b5a30f3fd6c
https://doi.org/10.1212/wnl.0b013e3181f4d7bf
https://doi.org/10.1212/wnl.0b013e3181f4d7bf
Autor:
Liesbet Deprez, Reana Velizarova, Arvid Suls, Jan Wauters, Albena Jordanova, Ivo Kremensky, P. De Jonghe, Velina Guergueltcheva, L Claes, T Van Dyck, Iglika Yordanova
Publikováno v:
Neurology
Objectives: The aim of this study was to determine the genetic defect in a 4-generational family with an epileptic disorder characterized by febrile and afebrile polymorphic seizures and mild to severe mental retardation by means of analyzing the neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bda29699adcd58b2ecd08609e5490148
https://doi.org/10.1212/wnl.0b013e3181e62088
https://doi.org/10.1212/wnl.0b013e3181e62088
Autor:
A Suls, T Van Dyck, Kristl Claeys, W. Van Paesschen, L Claes, Dominique Audenaert, Dirk Goossens, Liesbet Deprez, P. De Jonghe, K. Peeters, Jurgen Del-Favero
Publikováno v:
Neurology
Objective: To map the disease-causing locus in a large Belgian family with occipitotemporal lobe epilepsy associated with migraine with visual aura and to describe the clinical, electrophysiologic, and imaging characteristics. Methods: DNA samples fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14dbf1272ef30441da4f3b159675adf5
https://doi.org/10.1212/01.wnl.0000262764.78511.17
https://doi.org/10.1212/01.wnl.0000262764.78511.17
Autor:
Dominique Audenaert, Kristl G. Claeys, Lieven Lagae, E Schwartz, C. Van Broeckhoven, Robert L. Macdonald, Liesbet Deprez, P. De Jonghe, L Claes, T Van Dyck, Arvid Suls
Publikováno v:
Neurology
Mutations in the gene encoding the gamma2 subunit of the gamma-aminobutyric acid type A receptor (GABRG2) have been reported to cause childhood absence epilepsy (CAE), febrile seizures (FS), and generalized epilepsy with FS plus (GEFS+). The authors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::274876cf21b49e5a12f0cfe2386e6829
https://doi.org/10.1212/01.wnl.0000230145.73496.a2
https://doi.org/10.1212/01.wnl.0000230145.73496.a2
Publikováno v:
Equine Veterinary Journal. 28:421-424
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16b483830e98f15bef47df39d78d8641
https://doi.org/10.1111/j.2042-3306.1996.tb03116.x
https://doi.org/10.1111/j.2042-3306.1996.tb03116.x
Autor:
C. Van Broeckhoven, W. Van Paesschen, Kristl Claeys, Liesbet Deprez, Jurgen Del-Favero, L Claes, T Van Dyck, P. De Jonghe, Dirk Goossens, Dominique Audenaert
Publikováno v:
Journal of medical genetics
Generalised epilepsy with febrile seizures plus (GEFS+) is a clinically and genetically heterogeneous epilepsy syndrome. Using positional cloning strategies, mutations in SCN1B, SCN1A, and GABRG2 have been identified as genetic causes of GEFS+. In th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ee272b65d65bd8e957f13ffa4494dc6
https://pubmed.ncbi.nlm.nih.gov/15827091
https://pubmed.ncbi.nlm.nih.gov/15827091