Articles
121. Editorial: The role of glia in plasticity and behavior.
122. Reappraisal of Bergmann glial cells as modulators of cerebellar circuit function.
123. Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control.
124. Behavioral correlates of complex spike synchrony in cerebellar microzones.
De Gruijl JR, Hoogland TM, De Zeeuw CI
in The Journal of neuroscience : the official journal of the Society for Neuroscience 2014
125. Anomalous diffusion imposed by dendritic spines (Commentary on Santamaria et al.).
126. Cerebellar involvement in migraine.
Kros L, Angueyra Aristizábal CA, Khodakhah K
in Cephalalgia : an international journal of headache 2018
127. Expert versus proxy rating of verbal communicative ability of people with aphasia after stroke.
de Jong-Hagelstein M, Kros L, Lingsma HF, Dippel DW, Koudstaal PJ, Visch-Brink EG
in Journal of the International Neuropsychological Society : JINS 2012
128. The Sleeping Cerebellum.
129. Motor Learning Requires Purkinje Cell Synaptic Potentiation through Activation of AMPA-Receptor Subunit GluA3.
Gutierrez-Castellanos N, Da Silva-Matos CM, Zhou K, Canto CB, Renner MC, Koene LMC, Ozyildirim O, Sprengel R, Kessels HW, De Zeeuw CI
in Neuron 2017
130. Whole-Cell Properties of Cerebellar Nuclei Neurons In Vivo.
131. Flexible timing by temporal scaling of cortical responses.
132. The GABAA receptor is an FMRP target with therapeutic potential in fragile X syndrome.
Braat S, D'Hulst C, Heulens I, De Rubeis S, Mientjes E, Nelson DL, Willemsen R, Bagni C, Van Dam D, De Deyn PP, Kooy RF
in Cell cycle (Georgetown, Tex.) 2015
133. NPHP4 variants are associated with pleiotropic heart malformations.
French VM, van de Laar IM, Wessels MW, Rohe C, Roos-Hesselink JW, Wang G, Frohn-Mulder IM, Severijnen LA, de Graaf BM, Schot R, Breedveld G, Mientjes E, van Tienhoven M, Jadot E, Jiang Z, Verkerk A, Swagemakers S, Venselaar H, Rahimi Z, Najmabadi H, Meijers-Heijboer H, de Graaff E, Helbing WA, Willemsen R, Devriendt K, Belmont JW, Oostra BA, Amack JD, Bertoli-Avella AM
in Circulation research 2012
134. Excitatory Cerebellar Nucleocortical Circuit Provides Internal Amplification during Associative Conditioning.
Gao Z, Proietti-Onori M, Lin Z, Ten Brinke MM, Boele HJ, Potters JW, Ruigrok TJ, Hoebeek FE, De Zeeuw CI
in Neuron 2016
135. Discomfort and pain in newborns with myelomeningocele: a prospective evaluation.
136. Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1.
Rietman AB, van der Vaart T, Plasschaert E, Nicholson BA, Oostenbrink R, Krab LC, Descheemaeker MJ, Wit MY, Moll HA, Legius E, Nijs PFA
in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017
137. Epilepsy in children with tuberous sclerosis complex: Chance of remission and response to antiepileptic drugs.
Overwater IE, Bindels-de Heus K, Rietman AB, Ten Hoopen LW, Vergouwe Y, Moll HA, de Wit MC
in Epilepsia 2015
138. Regulating the human HECT E3 ligases.
139. Ageing shows a pattern of cerebellar degeneration analogous, but not equal, to that in patients suffering from cerebellar degenerative disease.
in NeuroImage 2015
140. Awareness of sensorimotor adaptation to visual rotations of different size.
in PloS one 2015
141. Behavioural and neural basis of anomalous motor learning in children with autism.
Marko MK, Crocetti D, Hulst T, Donchin O, Shadmehr R, Mostofsky SH
in Brain : a journal of neurology 2015
142. A Quick Assessment of Visuospatial Abilities in Adolescents Using the Design Organization Test (DOT).
143. Cerebellar transcranial direct current stimulation effects on saccade adaptation.
Avila E, van der Geest JN, Kengne Kamga S, Verhage MC, Donchin O, Frens MA
in Neural plasticity 2015
144. Small effects of neck torsion on healthy human voluntary eye movements.
in European journal of applied physiology 2013
145. A simplified protocol for differentiation of electrophysiologically mature neuronal networks from human induced pluripotent stem cells.
Gunhanlar N, Shpak G, van der Kroeg M, Gouty-Colomer LA, Munshi ST, Lendemeijer B, Ghazvini M, Dupont C, Hoogendijk WJG, Gribnau J, de Vrij FMS, Kushner SA
in Molecular psychiatry 2017
146. The SAC1 domain in synaptojanin is required for autophagosome maturation at presynaptic terminals.
Vanhauwaert R, Kuenen S, Masius R, Bademosi A, Manetsberger J, Schoovaerts N, Bounti L, Gontcharenko S, Swerts J, Vilain S, Picillo M, Barone P, Munshi ST, de Vrij FM, Kushner SA, Gounko NV, Mandemakers W, Bonifati V, Meunier FA, Soukup SF, Verstreken P
in The EMBO journal 2017
147. A rare missense variant in RCL1 segregates with depression in extended families.
Amin N, de Vrij FMS, Baghdadi M, Brouwer RWW, van Rooij JGJ, Jovanova O, Uitterlinden AG, Hofman A, Janssen HLA, Darwish Murad S, Kraaij R, Stedehouder J, van den Hout MCGN, Kros JM, van IJcken WFJ, Tiemeier H, Kushner SA, van Duijn CM
in Molecular psychiatry 2017
148. Hepatitis E Virus Infects Neurons and Brains.
Zhou X, Huang F, Xu L, Lin Z, de Vrij FMS, Ayo-Martin AC, van der Kroeg M, Zhao M, Yin Y, Wang W, Cao W, Wang Y, Kushner SA, Marie Peron J, Alric L, de Man RA, Jacobs BC, van Eijk JJ, Aronica EMA, Sprengers D, Metselaar HJ, de Zeeuw CI, Dalton HR, Kamar N, Peppelenbosch MP, Pan Q
in The Journal of infectious diseases 2017
149. Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.
Amin N, Jovanova O, Adams HH, Dehghan A, Kavousi M, Vernooij MW, Peeters RP, de Vrij FM, van der Lee SJ, van Rooij JG, van Leeuwen EM, Chaker L, Demirkan A, Hofman A, Brouwer RW, Kraaij R, Willems van Dijk K, Hankemeier T, van Ijcken WF, Uitterlinden AG, Niessen WJ, Franco OH, Kushner SA, Ikram MA, Tiemeier H, van Duijn CM
in Molecular psychiatry 2016
150. Subregion-specific dendritic spine abnormalities in the hippocampus of Fmr1 KO mice.
Levenga J, de Vrij FM, Buijsen RA, Li T, Nieuwenhuizen IM, Pop A, Oostra BA, Willemsen R
in Neurobiology of learning and memory 2011
151. Potential therapeutic interventions for fragile X syndrome.
152. Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons.
Levenga J, Buijsen RA, Rifé M, Moine H, Nelson DL, Oostra BA, Willemsen R, de Vrij FM
in Neurobiology of disease 2009
153. Transient and sustained afterdepolarizations in accessory olfactory bulb mitral cells are mediated by distinct mechanisms that are differentially regulated by neuromodulators.
Shpak G, Zylbertal A, Wagner S
in Frontiers in cellular neuroscience 2015
154. The levonorgestrel-releasing intrauterine device potentiates stress reactivity.
Aleknaviciute J, Tulen JHM, De Rijke YB, Bouwkamp CG, van der Kroeg M, Timmermans M, Wester VL, Bergink V, Hoogendijk WJG, Tiemeier H, van Rossum EFC, Kooiman CG, Kushner SA
in Psychoneuroendocrinology 2017
155. DNAJC6 Mutations Associated With Early-Onset Parkinson
Olgiati S, Quadri M, Fang M, Rood JP, Saute JA, Chien HF, Bouwkamp CG, Graafland J, Minneboo M, Breedveld GJ, Zhang J, Verheijen FW, Boon AJ, Kievit AJ, Jardim LB, Mandemakers W, Barbosa ER, Rieder CR, Leenders KL, Wang J, Bonifati V
in Annals of neurology 2016
156. Changing patterns in emergency involuntary admissions in the Netherlands in the period 2000-2004.
Mulder CL, Uitenbroek D, Broer J, Lendemeijer B, van Veldhuizen JR, van Tilburg W, Lelliott P, Wierdsma AI
in International journal of law and psychiatry 2008
157. Angiotensin II type 2 receptor- and acetylcholine-mediated relaxation: essential contribution of female sex hormones and chromosomes.
Pessôa BS, Slump DE, Ibrahimi K, Grefhorst A, van Veghel R, Garrelds IM, Roks AJ, Kushner SA, Danser AH, van Esch JH
in Hypertension (Dallas, Tex. : 1979) 2015
158. Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea.
159. Remote eye tracking assesses age dependence processing of coherent motion in typically-developing children.
in Journal of medical engineering & technology 2013
160. Synaptic vesicle dynamic changes in a model of fragile X
Broek JAC, Lin Z, de Gruiter HM, van 't Spijker H, Haasdijk ED, Cox D, Ozcan S, van Cappellen GWA, Houtsmuller AB, Willemsen R, de Zeeuw CI, Bahn S
in Molecular autism 2016
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