المؤلفون: Scott R; Instituto de Neurociencias, Consejo Superior de Investigaciones Científicas & Universidad Miguel Hernández, Sant Joan d'Alacant, Spain., Sánchez-Aguilera A; Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK., van Elst K; Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands., Lim L; Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK., Dehorter N; Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK., Bae SE; Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK., Bartolini G; Instituto de Neurociencias, Consejo Superior de Investigaciones Científicas & Universidad Miguel Hernández, Sant Joan d'Alacant, Spain.; Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK., Peles E; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel., Kas MJH; Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Groningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, The Netherlands., Bruining H; Department of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands., Marín O; Instituto de Neurociencias, Consejo Superior de Investigaciones Científicas & Universidad Miguel Hernández, Sant Joan d'Alacant, Spain.; Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.

المصدر: Cerebral cortex (New York, N.Y. : 1991) [Cereb Cortex] 2019 Feb 01; Vol. 29 (2), pp. 586-597.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Oxford University Press Country of Publication: United States NLM ID: 9110718 Publication Model: Print Cited Medium: Internet ISSN: 1460-2199 (Electronic) Linking ISSN: 10473211 NLM ISO Abbreviation: Cereb Cortex Subsets: MEDLINE

مواضيع طبية MeSH: Axons/*metabolism , Cerebral Cortex/*metabolism , Developmental Disabilities/*metabolism , Membrane Proteins/*deficiency , Nerve Fibers, Myelinated/*metabolism , Nerve Tissue Proteins/*deficiency , Stereotypic Movement Disorder/*metabolism, Action Potentials/physiology ; Animals ; Axons/pathology ; Cerebral Cortex/growth & development ; Cerebral Cortex/pathology ; Corpus Callosum/growth & development ; Corpus Callosum/metabolism ; Corpus Callosum/pathology ; Developmental Disabilities/genetics ; Developmental Disabilities/pathology ; Male ; Membrane Proteins/genetics ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Nerve Fibers, Myelinated/pathology ; Nerve Tissue Proteins/genetics ; Stereotypic Movement Disorder/genetics ; Stereotypic Movement Disorder/pathology ; Synaptic Transmission/physiology

المؤلفون: Hoch J; University of Minnesota hoch0048@umn.edu., Spofford L; University of Minnesota., Dimian A; University of Minnesota., Tervo R; Mayo Clinic., MacLean WE; University of Wisconsin., Symons FJ; University of Minnesota.

المصدر: Journal of pediatric psychology [J Pediatr Psychol] 2016 Jun; Vol. 41 (5), pp. 566-72. Date of Electronic Publication: 2015 Oct 29.

نوع المنشور: Comparative Study; Journal Article

بيانات الدورية: Publisher: Oxford University Press Country of Publication: United States NLM ID: 7801773 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1465-735X (Electronic) Linking ISSN: 01468693 NLM ISO Abbreviation: J Pediatr Psychol Subsets: MEDLINE

مواضيع طبية MeSH: Developmental Disabilities/*psychology , Self-Injurious Behavior/*etiology , Stereotypic Movement Disorder/*etiology, Case-Control Studies ; Child, Preschool ; Cross-Sectional Studies ; Female ; Humans ; Infant ; Male ; Prevalence ; Risk Factors ; Self-Injurious Behavior/diagnosis ; Self-Injurious Behavior/epidemiology ; Stereotypic Movement Disorder/diagnosis ; Stereotypic Movement Disorder/epidemiology

المؤلفون: Aliane V; INSERM U667, Collège de France, 11 place Marcelin Berthelot, Paris cedex 05, F-75231 France. marie-lou.kemel@college-de-france.fr., Pérez S, Bohren Y, Deniau JM, Kemel ML

المصدر: Brain : a journal of neurology [Brain] 2011 Jan; Vol. 134 (Pt 1), pp. 110-8. Date of Electronic Publication: 2010 Nov 19.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

مواضيع طبية MeSH: Acetylcholine/*metabolism , Corpus Striatum/*physiopathology , Interneurons/*physiology , Stereotypic Movement Disorder/*physiopathology, Analysis of Variance ; Animals ; Cholinergic Antagonists/pharmacology ; Cocaine ; Corpus Striatum/drug effects ; Corpus Striatum/metabolism ; Dopamine/metabolism ; Dopamine Antagonists/pharmacology ; Excitatory Amino Acid Agonists/pharmacology ; Interneurons/drug effects ; Male ; N-Methylaspartate/pharmacology ; Raclopride/pharmacology ; Rats ; Rats, Sprague-Dawley ; Scopolamine/pharmacology ; Stereotyped Behavior/drug effects ; Stereotypic Movement Disorder/chemically induced ; Stereotypic Movement Disorder/metabolism

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تسجيل الدخول للوصول الكامل.

المؤلفون: Cole, Allan Hugh, Jr., author

المصدر: Counseling Persons with Parkinson's Disease, 2021.

الإتاحة: https://doi.org/10.1093/oso/9780190672928.003.0005

المؤلفون: Cole, Allan Hugh, Jr., author

المصدر: Counseling Persons with Parkinson's Disease, 2021.

الإتاحة: https://doi.org/10.1093/oso/9780190672928.003.0001

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تسجيل الدخول للوصول الكامل.

المؤلفون: Daniëlle G. M. Bosch, Nicole Corsten-Janssen, Colin A Ellis, Dirk Lefeber, Alfredo Brusco, Irene Bagnasco, Andrea Accogli, Ellen Macnamara, Carlo Di Bonaventura, Giovanna Zorzi, Scott Demarest, Erik A. Eklund, Noëlle Mercier, Carlo Marcelis, Rong Zhang, Ban H Edani, Camilo Toro, Ziv Gan-Or, Simone Pizzi, Kariona A. Grabińska, Nienke E. Verbeek, Karen W. Gripp, Simone Martinelli, Caterina Caputi, Luca Pannone, Marco Tartaglia, Felix Distelmaier, Louise Amlie-Wolf, Luisa Averdunk, Anne-Sophie Alaix, Renzo Guerrini, Laura Masuelli, Marwan Shinawi, Sunita Venkateswaran, Joseph Peeden, Hana Hansikova, Lucie Zdrazilova, William C. Sessa, Serena Galosi, Renske Oegema, Patricia G Wheeler, Kristin W. Barañano, Vincenzo Leuzzi, Frances Elmslie, Fadi F. Hamdan, Roberto Bei, Jean-Marc Good, Isis Atallah, Myriam Srour, Erik-Jan Kamsteeg

المصدر: Brain, 145, 1, pp. 208-223
Brain
Brain, 145(1), 208-223. Oxford University Press
Brain, vol. 145, no. 1, pp. 208-223
Brain, 145, 208-223

مصطلحات موضوعية: Myoclonus, Ataxia, Retinitis, Progressive myoclonus epilepsy, congenital disorders of glycosylation, dolichol, movement disorder, myoclonus epilepsy, neurodegenerative disorder, DHDDS, Biology, Settore MED/04, Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12], chemistry.chemical_compound, Neurodevelopmental disorder, Dolichol, Dolichols, Retinitis pigmentosa, medicine, Alkyl and Aryl Transferases, Child, Dolichols/metabolism, Humans, Neurodegenerative Diseases/genetics, Retinitis Pigmentosa/genetics, PROTEIN GLYCOSYLATION, MUTATION, NOGO-B RECEPTOR, CIS-PRENYLTRANSFERASE, Genetics, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Neurodegenerative Diseases, LOCALIZATION, medicine.disease, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], OLIGOSACCHARIDES, INSIGHTS, chemistry, Neuronal ceroid lipofuscinosis, Original Article, Neurology (clinical), medicine.symptom, LIQUID-CHROMATOGRAPHY, Retinitis Pigmentosa, GENETIC-DEFECTS

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::012cb40531119a7d00e4415b8540c52c
https://research.rug.nl/en/publications/50de5bd9-24f7-4573-b0f2-fed69db9588d

المؤلفون: Kailash P. Bhatia, Patrick Haggard, Mark J. Edwards, Anne-Catherine M L Huys

المصدر: Brain

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, media_common.quotation_subject, Neurological disorder, Physical medicine and rehabilitation, functional neurological disorder, functional movement disorder, Distraction, Tremor, medicine, Humans, Contrast (vision), Functional movement disorder, Aged, media_common, Focus (computing), visual feedback, treatment, AcademicSubjects/SCI01870, Movement (music), Motor control, Original Articles, Middle Aged, medicine.disease, Action tremor, attention, Conversion Disorder, Female, AcademicSubjects/MED00310, Neurology (clinical), Psychology, Psychomotor Performance

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::277d718d175f37cc752e6cc9f75edef4
https://openaccess.sgul.ac.uk/id/eprint/113387/11/awab230.pdf

المؤلفون: Gotman, Kélina, author

المصدر: Choreomania : Dance and Disorder, 2018.

الإتاحة: https://doi.org/10.1093/oso/9780190840419.003.0009