Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Zeeuw, C.I. de"'
Autor:
Sande, E. van der, Haarman, A.E.G., Quint, W.H., Tadema, K.C.D., Meester-Smoor, M.A., Kamermans, M., Zeeuw, C.I. de, Klaver, C.C.W., Winkelman, B.H.J., Iglesias, A.I.
Publikováno v:
Investigative Ophthalmology & Visual Science, 63(3):5. Association for Research in Vision and Ophthalmology Inc.
Investigative Ophthalmology and Visual Science, 63
Investigative Ophthalmology and Visual Science, 63, 3
Investigative Ophthalmology and Visual Science, 63
Investigative Ophthalmology and Visual Science, 63, 3
Contains fulltext : 249591.pdf (Publisher’s version ) (Open Access) Refractive errors are common eye disorders characterized by a mismatch between the focal power of the eye and its axial length. An increased axial length is a common cause of the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1132b44c3fac414e4f983ad98dbd11a7
http://www.scopus.com/inward/record.url?scp=85126081107&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85126081107&partnerID=8YFLogxK
Autor:
Sun, J., Alphen, A.M. van, Wagenaar, M., Huygen, P.L.M., Hoogenraad, C.C., Hasson, T., Koekkoek, S.K., Bohne, B.A., Zeeuw, C.I. de
Publikováno v:
Annals of the New York Academy of Sciences, 942, pp. 493--6
Annals of the New York Academy of Sciences, 942, 493--6
Annals of the New York Academy of Sciences, 942, 493--6
Item does not contain fulltext Identification of genes involved in hereditary vestibular disease is growing at a remarkable pace. Mutant mouse technology can be an important tool for understanding the biological mechanism of human vestibular diseases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::633510c87841323b210146c5e43284ee
https://hdl.handle.net/2066/144655
https://hdl.handle.net/2066/144655
Autor:
Kelders, W.P.A., Kleinrensink, G.J., Geest, J.N. Van Der, Schipper, I.B., Feenstra, L., Zeeuw, C.I. De, Frens, M.A.
Publikováno v:
Journal of Neurotrauma; January 2005, Vol. 22 Issue: 1 p133-137, 5p
Publikováno v:
Genes and Function; June 1997, Vol. 1 Issue: 3 p175-190, 16p
Autor:
Koppen, H., Palm-Meinders, H., Koutstaal, B., Boele, H.J., Koekoek, B.K., Geest, J. van der, Launer, L.J., Buchem, M.A. van, Terwindt, G.M., Ferrari, M.D., Kruit, M.C., Zeeuw, C.I. de
Publikováno v:
Publons
ResearcherID
Cephalalgia, 33(S8), 228-228
ResearcherID
Cephalalgia, 33(S8), 228-228
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0150abd83841d071f60c765cab5d41ca
https://publons.com/publon/12590051/
https://publons.com/publon/12590051/
Autor:
Koppen, H.
Publikováno v:
None
The association between migraine and silent ischemic brain lesions was investigated. Also the occurence of right-to-left shunts in different migraine groups and controls. The functional consequences of silent ischemic brain lesions were investigated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1e372bd4c2535621562e9f6c081f9fe6
http://hdl.handle.net/1887/61048
http://hdl.handle.net/1887/61048
Autor:
Meinders, I.H.
Publikováno v:
None
This thesis describes the longitudinal population-based CAMERA-study on the association between migraine and brain changes (e.g. white matter hyperintensities, infarct-like and other lesions) and possible causes and consequences of those brain change
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2fdf24a3f96b0e9cc2ab9a8432141fec
https://hdl.handle.net/1887/61147
https://hdl.handle.net/1887/61147
Autor:
Todorov, B.B.
Publikováno v:
None
The aim of the studies described in this thesis was to investigate how abnormal CaV2.1 channel function can cause disease, in particular motor coordination dysfunction. The chapters illustrate how various neuronal cell types in the periphery (periphe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e69627a41c4ec503c4432a0babe0c6f0
https://hdl.handle.net/1887/15580
https://hdl.handle.net/1887/15580