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1. Full Text Medication overuse headache: An ongoing debate
by Louter, Mark A and Robbins, Matthew S and Terwindt, Gisela M
Neurology, ISSN 0028-3878, 09/2017, Volume 89, Issue 12, pp. 1206 - 1207
DETOXIFICATION | CLINICAL NEUROLOGY | Index Medicus | Abridged Index Medicus
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2. Full Text Advance in genetics of migraine
by de Boer, Irene and van den Maagdenberg, Arn M J M and Terwindt, Gisela M
Current opinion in neurology, ISSN 1350-7540, 06/2019, Volume 32, Issue 3, pp. 413 - 421
Migraine is a primary headache disorder and one of the most common and disabling neurological diseases worldwide. Genome-wide association studies have... 
Genome-wide association studies | Genetic aspects | Research | Analysis | Migraine | Edited by Messoud Ashina and Henrik Winther Schytz | genetics | migraine | HEADACHE | genome-wide association study | hemiplegic migraine | depression
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3. Full Text Acute withdrawal and botulinum toxin A in chronic migraine with medication overuse: a double-blind randomized controlled trial
by Pijpers, Judith A and Kies, Dennis A and Louter, Mark A and van Zwet, Erik W and Ferrari, Michel D and Terwindt, Gisela M
Brain, ISSN 0006-8950, 05/2019, Volume 142, Issue 5, pp. 1203 - 1214
Botox is widely used in chronic migraine although efficacy in studies was only modest and likely confounded by unblinding. In a randomised, double-blind,... 
Clinical Trial | botulinum toxin A | Editor's Choice | medication overuse | withdrawal | chronic migraine | detoxification
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4. Full Text MRI evaluation of the relationship between carotid artery endothelial shear stress and brain white matter lesions in migraine
by Hoogeveen, Evelien S and Arkink, Enrico B and van der Grond, Jeroen and van Buchem, Mark A and Ferrari, Michel D and Terwindt, Gisela M and Kruit, Mark C and PROSPER Study Group and On Behalf of the PROSPER Study Group
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, ISSN 0271-678X, 06/2019, pp. 271678X19857810 - 271678X19857810
Although white matter lesions are frequently detected in migraine patients, underlying mechanisms remain unclear. Low carotid artery endothelial shear stress... 
magnetic resonance imaging | migraine | endothelial shear stress | Cerebrovascular disease | hemodynamics
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5. Full Text Brain atrophy following hemiplegic migraine attacks
by Pelzer, Nadine and Hoogeveen, Evelien S and Ferrari, Michel D and Poll-The, Bwee Tien and Kruit, Mark C and Terwindt, Gisela M
Cephalalgia, ISSN 0333-1024, 2017
Background Patients with hemiplegic migraine (HM) may sometimes develop progressive neurological deterioration of which the pathophysiology is unknown. Patient... 
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6. Full Text In silicophenotyping via co-training for improved phenotype prediction from genotype
by Roqueiro, Damian and Witteveen, Menno J and Anttila, Verneri and Terwindt, Gisela M and van den Maagdenberg, Arn M.J.M and Borgwardt, Karsten
Bioinformatics, ISSN 1367-4803, 06/2015, Volume 31, Issue 12, pp. i303 - i310
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7. Hoofdpijn door overgebruik van pijnmedicatie
by Pijpers, Judith A and Wiendels, Natalie J and Koppen, Hille and Ferrari, Michel D and Haan, Joost and Terwindt, Gisela M
Nederlands Tijdschrift voor Geneeskunde, ISSN 0028-2162, 2018, Volume 162, Issue 6
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8. Full Text Ethanol contamination of cerebrospinal fluid during standardized sampling and its effect on ^sup 1^H-NMR metabolomics
by Sonia A van der Sar and Ronald Zielman and Gisela M Terwindt and Arn M J M van den Maagdenberg and André M Deelder and Oleg A Mayboroda and Axel Meissner and Michel D Ferrari
Analytical and Bioanalytical Chemistry, ISSN 1618-2642, 06/2015, Volume 407, Issue 16, p. 4835
  Issue Title: Expanding the team of ABC Editors/Studying human decomposition signatures/SIMS detection of organic nanoparticles in cells/Spatial... 
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9. Full Text Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
by Gormley, A.M and Stefansson, Hreinn and Winsvold, Bendik and Palta, Priit and Esko, Tõnu and Pers, Tune and Farh, Kai-How and Cuenca-Leon, E and Muona, M and Furlotte, N.A and Kurth, Karl and Ingason, Anes and Mcmahon, George and Ligthart, Lannie and Terwindt, Gisela and Todt, Unda and Müller-Myhsok, Bertram and Ran, C and Gordon, S.G and Stam, Anine and Steinberg, Stacy and Göbel, Hartmut and Koiranen, Markku and Quaye, Lydia and Adams, H.H.H and Lehtimäki, Terho and Sarin, A.-P and Wedenoja, J and Hinds, David A and Buring, J.E and Schürks, Markus and Ridker, Paul and Hrafnsdottir, M.G and Ring, Susan and Hottenga, Jouke Jan and Penninx, Brenda and Färkkilä, Markus and Artto, Ville and Hämäläinen, Eija and Lucae, Susanne and Malik, Rainer and Heath, Anew C and Madden, Pamela and Martin, Nicholas and Montgomery, Grant and Kurki, M.I and Kals, Mart and Mägi, Reedik and Pärn, K and Hamalainen, Eija and Huang, H and Byrnes, A.E and Franke, Lude and Huang, Jian and Stergiakouli, Evangelia and Lee, Phil and Sandor, C and Webber, C and Cader, Z and Müller-Myhsok, B and Schreiber, Stefan and Meitinger, Thomas and Hagen, Knut and Salomaa, Veikko and Heikkilä, Kauko and Loehrer, Elizabeth and Uitterlinden, Ané and Hofman, A and Duijn, Cornelia and Cherkas, Lynn and Pedersen, L.M and Stubhaug, A and Nielsen, C.S and Männikkö, M and Mihailov, Evelin and Milani, Lili and Esserlind, A.-L and Christensen, A.F and Hansen, T.F and Werge, Thomas and Kaprio, Jaakko and Aromaa, Arpo and Raitakari, Olli and Ikram, Arfan and Ikram, Kamran and Jarvelin, Marjo-Riitta and Metspalu, Anes and Kubisch, Christian and Strachan, David and Ferrari, Michel and Belin, A.C and Wessman, Maija and Maagdenberg, Arn and Zwart, John-Anker and Boomsma, Dorret and Smith, G.D and Stefansson, K and Eriksson, Nicholas and Daly, Mark and Neale, Benjamin and ... and Int Headache Genetics Consortium and International Headache Genetics Consortium
Nature Genetics, ISSN 1061-4036, 08/2016, Volume 48, Issue 8, pp. 856 - 866
textabstractMigraine is a debilitating neurological disorder affecting around one in seven people worldwide, but its molecular mechanisms remain poorly... 
SYSTEMATIC ANALYSIS | MYOCARDIAL-INFARCTION | GENOTYPE IMPUTATION | GENETICS & HEREDITY | GENE-EXPRESSION | SMOOTH-MUSCLE-CELLS | FAMILIAL HEMIPLEGIC MIGRAINE | RECEPTOR-RELATED PROTEIN-1 | SINGLE-NUCLEOTIDE POLYMORPHISMS | SPREADING DEPRESSION | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Migraine Disorders - genetics | Genetic Markers - genetics | Genomics | Humans | Genetic Loci - genetics | Polymorphism, Single Nucleotide - genetics | Vascular Diseases - genetics | Muscle, Smooth - metabolism | Case-Control Studies | Quantitative trait loci | Genome-wide association studies | Migraine | Genetic aspects | Gene expression | Identification and classification | Health aspects | Risk factors | Methods | Studies | Confidence intervals | Consortia | Headaches | Gene loci | Genomes | Meta-analysis | Index Medicus
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10. Full Text Analysis of shared heritability in common disorders of the brain
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Index Medicus | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
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11. Hoger cardiovasculair risico bij vrouwen met migraine: Wat zijn de consequenties voor de begeleiding van jonge patiënten?
by Linstra, Katie M and Wermer, Marieke J.H and Terwindt, Gisela M
Nederlands Tijdschrift voor Geneeskunde, ISSN 0028-2162, 2017, Volume 161, Issue 17
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12. Full Text Genome-wide association study reveals three susceptibility loci for common migraine in the general population
by Kubisch, Christian and Schürks, Markus and Palotie, Aarno and de Vries, Boukje and Buring, Julie E and Chasman, Daniel I and Ernst, Florian and Griffiths, Lyn R and Völzke, Henry and Launer, Lenore J and Schminke, Ulf and Freilinger, Tobias and van den Maagdenberg, Arn M J M and Ridker, Paul M and Hoffmann, Wolfgang and Ferrari, Michel D and Zee, Robert Y L and Anttila, Verneri and Kurth, Tobias and Fendrich, Konstanze and Kallela, Mikko and Terwindt, Gisela M and IHGC
Nature Genetics, ISSN 1061-4036, 07/2011, Volume 43, Issue 7, pp. 695 - 698
Migraine is a common, heterogeneous and heritable neurological disorder. Its pathophysiology is incompletely understood, and its genetic influences at the... 
NEUROPATHIC PAIN | GENOTYPE IMPUTATION | PACKAGE | GENETICS & HEREDITY | SNPS | RECEPTOR | COHORT | HEALTH | TOOL | United States - epidemiology | Genetic Predisposition to Disease | Genome-Wide Association Study | Prognosis | Humans | Middle Aged | Risk Factors | Male | Genetic Loci | Case-Control Studies | Migraine without Aura - genetics | Chromosomes, Human, Pair 2 - genetics | Migraine without Aura - pathology | Polymorphism, Single Nucleotide - genetics | Female | Chromosomes, Human, Pair 1 - genetics | Migraine without Aura - epidemiology | Chromosomes, Human, Pair 12 - genetics | Cohort Studies | Genetic aspects | Research | Genetic susceptibility | Migraine | Risk factors | Confidence intervals | Genealogy | Womens health | Headaches | Genetics | Genomes | Epidemiology | Meta-analysis | Index Medicus
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13. Full Text Cortical atrophy in patients with cerebral amyloid angiopathy: a case-control study
by Fotiadis, Panagiotis, BS and van Rooden, Sanneke, PhD and van der Grond, Jeroen, PhD and Schultz, Aaron, PhD and Martinez-Ramirez, Sergi, MD and Auriel, Eitan, MD and Reijmer, Yael, PhD and van Opstal, Anna M, PhD and Ayres, Alison, BA and Schwab, Kristin M, BA and Alzheimer's Disease Neuroimaging Initiative (ADNI) and Hedden, Trey, PhD and Rosand, Jonathan, Prof and Viswanathan, Anand, MD and Wermer, Marieke, MD and Terwindt, Gisela M, MD and Sperling, Reisa A, Prof and Polimeni, Jonathan R, PhD and Johnson, Keith A, Prof and van Buchem, Mark A, Prof and Greenberg, Steven M, Prof and Gurol, M Edip, Dr and Alzheimer's Dis Neuroimaging Initi and Alzheimer's Disease Neuroimaging Initiative
Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 8, pp. 811 - 819
Summary Background Loss of cortical grey matter is a diagnostic marker of many neurodegenerative diseases, and is a key mediator of cognitive impairment. We... 
Neurology | SURFACE-BASED ANALYSIS | SMALL VESSEL DISEASE | DUTCH-TYPE | MICROBLEEDS | HEREDITARY | ALZHEIMERS-DISEASE | CLINICAL-DIAGNOSIS | SEGMENTATION | BOSTON CRITERIA | BRAIN | CLINICAL NEUROLOGY | Atrophy - diagnostic imaging | Cerebral Amyloid Angiopathy - diagnostic imaging | Humans | Middle Aged | Cerebral Cortex - pathology | Linear Models | Male | Atrophy - etiology | Amyloidosis - diagnostic imaging | Cerebral Hemorrhage - diagnostic imaging | Case-Control Studies | Cerebral Cortex - diagnostic imaging | Magnetic Resonance Imaging | Cerebral Amyloid Angiopathy - complications | Image Processing, Computer-Assisted | Statistics, Nonparametric | Adult | Female | Aged | Amyloidosis - etiology | Retrospective Studies | Cerebral Amyloid Angiopathy - genetics | Cerebral Hemorrhage - etiology | Medicine, Experimental | Medical research | Nervous system diseases | Care and treatment | Amyloidosis | Alzheimer's disease | Studies | Pathology | Hospitals | Medical imaging | Cognitive ability | Mutation | Alzheimers disease | Age | Index Medicus
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14. Full Text The International Classification of Headache Disorders, 3rd edition (beta version)
by Olesen, Jes and Bes, André and Kunkel, Robert and Lance, James W and Nappi, Giuseppe and Pfaffenrath, Volker and Rose, Frank Clifford and Schoenberg, Bruce S and Soyka, Dieter and Tfelt-Hansen, Peer and Welch, K. Michael A and Wilkinson, Marica and Bousser, Marie-Germaine and Diener, Hans-Christoph and Dodick, David and First, Michael and Goadsby, Peter J and Göbel, Hartmut and Lainez, Miguel J. A and Lipton, Richard B and Sakai, Fumihiko and Schoenen, Jean and Silberstein, Stephen D and Steiner, Timothy J and Bendtsen, Lars and Ducros, Anne and Evers, Stefan and Hershey, Andrew and Katsarava, Zaza and Levin, Morris and Pascual, Julio and Russell, Michael B and Schwedt, Todd and Tassorelli, Cristina and Terwindt, Gisela M and Vincent, Maurice and Wang, Shuu-Jiun and Charles, A and Lipton, R and Bolay, H and Lantéri-Minet, M and Macgregor, E.A and Takeshima, T and Schytz, H.W and Ashina, S and Goicochea, M.T and Hirata, K and Holroyd, K and Lampl, C and Mitsikostas, D.D and Goadsby, P and Boes, C and Bordini, C and Cittadini, E and Cohen, A and Leone, M and May, A and Newman, L and Pareja, J and Park, J.-W and Rozen, T and Waldenlind, E and Fuh, J.-L and Ozge, A and Pareja, J.A and Peres, M and Young, W and Yu, S.-Y and Abu-Arafeh, I and Gladstone, J and Huang, S.-J and Jensen, R and Lainez, J.M.A and Obelieniene, D and Sandor, P and Scher, A.I and Arnold, M and Dichgans, M and Houdart, E and Ferro, J and Leroux, E and Li, Y.-S and Singhal, A and Tietjen, G and Friedman, D and Kirby, S and Mokri, B and Purdy, A and Ravishankar, K and Schievink, W and Stark, R and Taylor, F and Krymchantowski, A.V and Tugrul, A and Wiendels, N.J and Marchioni, E and Osipova, V and Savi, L and Berger, J.R and Bigal, M and ... and IHS and Headache Classification Committee of the International Headache Society (IHS)
Cephalalgia, ISSN 0333-1024, 7/2013, Volume 33, Issue 9, pp. 629 - 808
TRAUMATIC BRAIN-INJURY | TENSION-TYPE HEADACHE | ICE-CREAM HEADACHE | MEDICATION-OVERUSE HEADACHE | CENTRAL-NERVOUS-SYSTEM | DAILY-PERSISTENT HEADACHE | TOLOSA-HUNT-SYNDROME | MYOFASCIAL TRIGGER POINTS | FAMILIAL HEMIPLEGIC MIGRAINE | NEUROSCIENCES | CLINICAL NEUROLOGY | CHRONIC PAROXYSMAL HEMICRANIA | International Classification of Diseases | Headache Disorders - classification | Humans | Index Medicus
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