His primary areas of investigation include Epilepsy, Pediatrics, Genetics, Magnetoencephalography and Central nervous system disease. His Epilepsy research is mostly focused on the topic Lamotrigine. Patrick Van Bogaert has researched Pediatrics in several fields, including Surgery, Febrile seizure, Dravet syndrome, Slow-wave sleep and Intelligence quotient.
His research integrates issues of Computer vision, Index finger, Communication and Artificial intelligence in his study of Magnetoencephalography. His work in Artificial intelligence covers topics such as Pattern recognition which are related to areas like Electroencephalography. Patrick Van Bogaert interconnects Positron emission tomography, Nuclear medicine, Neurological examination and Magnetic resonance imaging in the investigation of issues within Central nervous system disease.
Patrick Van Bogaert mainly focuses on Epilepsy, Neuroscience, Electroencephalography, Magnetoencephalography and Pediatrics. His studies in Epilepsy integrate themes in fields like Anesthesia and Audiology. Many of his studies involve connections with topics such as Hypermetabolism and Neuroscience.
His research investigates the link between Electroencephalography and topics such as Pattern recognition that cross with problems in Entropy and Resting state fMRI. Patrick Van Bogaert combines subjects such as Motor cortex and Artificial intelligence with his study of Magnetoencephalography. His Pediatrics study typically links adjacent topics like Psychiatry.
Epilepsy, Electroencephalography, Neuroscience, Magnetoencephalography and Pediatrics are his primary areas of study. Patrick Van Bogaert works in the field of Epilepsy, focusing on Ictal in particular. His study in Electroencephalography is interdisciplinary in nature, drawing from both Entropy, Artificial intelligence, Pattern recognition, Functional neuroimaging and Receiver operating characteristic.
His Magnetoencephalography study combines topics from a wide range of disciplines, such as Somatosensory system, Communication, Rhythm, Resting state fMRI and Brain activity and meditation. The Pediatrics study combines topics in areas such as Gestational age, Prospective cohort study, Disease, Epileptic spasms and Myoclonus. His Audiology research incorporates themes from Aphasia, Landau–Kleffner syndrome and Rolandic epilepsy.
His primary scientific interests are in Magnetoencephalography, Epilepsy, Audiology, Brain activity and meditation and Artificial intelligence. His Magnetoencephalography study is concerned with the larger field of Neuroscience. His study of Dravet syndrome is a part of Epilepsy.
His Audiology research incorporates elements of Recall, Prosody, Memory consolidation and Temporal lobe. His Artificial intelligence research includes themes of Computer vision, Superior parietal lobule, Human brain and Pattern recognition. His study looks at the relationship between Pattern recognition and topics such as Brain mapping, which overlap with Electroencephalography.
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Glucose transporter-1 deficiency syndrome: The expanding clinical and genetic spectrum of a treatable disorder
Wilhelmina G. Leen;Joerg Klepper;Marcel M. Verbeek;Maike Leferink.
Summary of recommendations for the management of infantile seizures: Task Force Report for the ILAE Commission of Pediatrics.
Jo M. Wilmshurst;William D. Gaillard;Kollencheri Puthenveettil Vinayan;Tammy N. Tsuchida.
The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway
Hsien-Yang Lee;Ying Xu;Yong Huang;Andrew H. Ahn.
Human Molecular Genetics (2004)
Levetiracetam efficacy in epileptic syndromes with continuous spikes and waves during slow sleep: experience in 12 cases.
Alec Aeby;Nathalie Poznanski;Denis Verheulpen;Catherine Wetzburger.
Corticosteroids as treatment of epileptic syndromes with continuous spike‐waves during slow‐wave sleep
Marga Buzatu;Christine Bulteau;Cécilia Altuzarra;Olivier Dulac.
Vagus nerve stimulation for refractory epilepsy: a Belgian multicenter study.
Veerle De Herdt;Paul Boon;Berten Ceulemans;Henri Hauman.
European Journal of Paediatric Neurology (2007)
Agenesis of corpus callosum: prenatal diagnosis and prognosis
Marie-Laure Moutard;Virginie Kieffer;Josué Feingold;François Kieffer.
Childs Nervous System (2003)
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.
Katayoun Vahedi;Anne Joutel;Patrick van Bogaert;Anne Ducros.
Annals of Neurology (1995)
Genetic spectrum of hereditary neuropathies with onset in the first year of life
Jonathan Baets;Tine Deconinck;Els De Vriendt;Magdalena Zimoń.
Brain function in the vegetative state
Steven Laureys;Sylvie Antoine;Melanie Boly;Sandra Elincx.
Acta Neurologica Belgica (2004)
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