المؤلفون: Dennis Lal, Ann-Kathrin Ruppert, Holger Trucks, Herbert Schulz, Carolien G de Kovel, Dorothée Kasteleijn-Nolst Trenité, Anja C M Sonsma, Bobby P Koeleman, Dick Lindhout, Yvonne G Weber, Holger Lerche, Claudia Kapser, Christoph J Schankin, Wolfram S Kunz, Rainer Surges, Christian E Elger, Verena Gaus, Bettina Schmitz, Ingo Helbig, Hiltrud Muhle, Ulrich Stephani, Karl M Klein, Felix Rosenow, Bernd A Neubauer, Eva M Reinthaler, Fritz Zimprich, Martha Feucht, Rikke S Møller, Helle Hjalgrim, Peter De Jonghe, Arvid Suls, Wolfgang Lieb, Andre Franke, Konstantin Strauch, Christian Gieger, Claudia Schurmann, Ulf Schminke, Peter Nürnberg, EPICURE Consortium, Thomas Sander

المصدر: PLoS Genetics, Vol 11, Iss 5, p e1005226 (2015)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/7a9aaf42fe42407c9b6b46e8e6a9130a

المؤلفون: Nienke E Verbeek, Nicoline A T van der Maas, Floor E Jansen, Marjan J A van Kempen, Dick Lindhout, Eva H Brilstra

المصدر: PLoS ONE, Vol 8, Iss 6, p e65758 (2013)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3675088?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/14f2bd90feec41f79dcf92811e02b9bb

المؤلفون: Schijven D., Stevelink R., McCormack M., van Rheenen W., Luykx J. J., Koeleman B. P. C., Veldink J. H., Aleksey Shatunov, Russell L. McLaughlin, Rick A. A. van der Spek, Alfredo Iacoangeli, Kevin P. Kenna, Kristel R. van Eijk, Nicola Ticozzi, Boris Rogelj, Katarina Vrabec, Metka Ravnik-Glavač, Blaž Koritnik, Janez Zidar, Lea Leonardis, Leja Dolenc Grošelj, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Marta Gromicho, Ana Pronto-Laborinho, Jesus S. Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen E. Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Alan Pittman, Katie Sidle, Pietro Fratta, Andrea Malaspina, Simon Topp, Susanne Petri, Susanna Abdulla, Carsten Drepper, Michael Sendtner, Thomas Meyer, Roel A. Ophoff, Kim A. Staats, Martina Wiedau-Pazos, Catherine Lomen-Hoerth, Vivianna M. Van Deerlin, John Q. Trojanowski, Lauren Elman, Leo McCluskey, A. Nazli Basak, Thomas Meitinger, Peter Lichtner, Milena Blagojevic-Radivojkov, Christian R. Andres, Gilbert Bensimon, Bernhard Landwehrmeyer, Alexis Brice, Christine A. M. Payan, Safaa Saker-Delye, Alexandra Dürr, Nicholas W. Wood, Lukas Tittmann, Wolfgang Lieb, Andre Franke, Marcella Rietschel, Sven Cichon, Markus M. Nöthen, Philippe Amouyel, Christophe Tzourio, Jean-François Dartigues, Andre G. Uitterlinden, Fernando Rivadeneira, Karol Estrada, Albert Hofman, Charles Curtis, Anneke J. van der Kooi, Markus Weber, Christopher E. Shaw, Bradley N. Smith, Daisy Sproviero, Cristina Cereda, Mauro Ceroni, Luca Diamanti, Roberto Del Bo, Stefania Corti, Giacomo P. Comi, Sandra D'Alfonso, Lucia Corrado, Cinzia Bertolin, Gianni Sorarù, Letizia Mazzini, Viviana Pensato, Cinzia Gellera, Cinzia Tiloca, Antonia Ratti, Andrea Calvo, Cristina Moglia, Maura Brunetti, Simona Arcuti, Rosa Capozzo, Chiara Zecca, Christian Lunetta, Silvana Penco, Nilo Riva, Alessandro Padovani, Massimiliano Filosto, Ian Blair, Garth A. Nicholson, Dominic B. Rowe, Roger Pamphlett, Matthew C. Kiernan, Julian Grosskreutz, Otto W. Witte, Robert Steinbach, Tino Prell, Beatrice Stubendorff, Ingo Kurth, Christian A. Hübner, P. Nigel Leigh, Federico Casale, Adriano Chio, Ettore Beghi, Elisabetta Pupillo, Rosanna Tortelli, Giancarlo Logroscino, John Powell, Albert C. Ludolph, Jochen H. Weishaupt, Wim Robberecht, Philip Van Damme, Robert H. Brown, Jonathan D. Glass, John E. Landers, Orla Hardiman, Peter M. Andersen, Philippe Corcia, Patrick Vourc'h, Vincenzo Silani, Michael A. van Es, R. Jeroen Pasterkamp, Cathryn M. Lewis, Gerome Breen, Ammar Al-Chalabi, Leonard H. van den Berg, Jan H. Veldink, Daniela Calini, Isabella Fogh, Barbara Castellotti, Franco Taroni, Stella Gagliardi, Giacomo Comi, Sandra D’Alfonso, Elena Pegoraro, Giorgia Querin, Francesca Gerardi, Fabrizio Rinaldi, Maria Sofia Cotelli, Luca Chiveri, Maria Cristina Guaita, Patrizia Perrone, Giancarlo Comi, Carlo Ferrarese, Lucio Tremolizzo, Marialuisa Delodovici, Giorgio Bono, Stefania Cammarosano, Antonio Canosa, Dario Cocito, Leonardo Lopiano, Luca Durelli, Bruno Ferrero, Antonio Bertolotto, Alessandro Mauro, Luca Pradotto, Roberto Cantello, Enrica Bersano, Dario Giobbe, Maurizio Gionco, Daniela Leotta, Lucia Appendino, Cavallo Cavallo, Enrico Odddenino, Claudio Geda, Fabio Poglio, Paola Santimaria, Umberto Massazza, Antonio Villani, Roberto Conti, Fabrizio Pisano, Mario Palermo, Franco Vergnano, Paolo Provera, Maria Teresa Penza, Marco Aguggia, Nicoletta Di Vito, Piero Meineri, Ilaria Pastore, Paolo Ghiglione, Danilo Seliak, Nicola Launaro, Giovanni Astegiano, Bottacchi Edo, Isabella Laura Simone, Stefano Zoccolella, Michele Zarrelli, Franco Apollo, William Camu, Jean Sebastien Hulot, Francois Viallet, Philippe Couratier, David Maltete, Christine Tranchant, Marie Vidailhet, Bassel Abou-Khalil, Pauls Auce, Andreja Avbersek, Melanie Bahlo, David J Balding, Thomas Bast, Larry Baum, Albert J Becker, Felicitas Becker, Bianca Berghuis, Samuel F Berkovic, Katja E Boysen, Jonathan P Bradfield, Lawrence C Brody, Russell J Buono, Ellen Campbell, Gregory D Cascino, Claudia B Catarino, Gianpiero L Cavalleri, Stacey S Cherny, Krishna Chinthapalli, Alison J Coffey, Alastair Compston, Antonietta Coppola, Patrick Cossette, John J Craig, Gerrit-Jan de Haan, Peter De Jonghe, Carolien G F de Kovel, Norman Delanty, Chantal Depondt, Orrin Devinsky, Dennis J Dlugos, Colin P Doherty, Christian E Elger, Johan G Eriksson, Thomas N Ferraro, Martha Feucht, Ben Francis, Jacqueline A French, Saskia Freytag, Verena Gaus, Eric B Geller, Christian Gieger, Tracy Glauser, Simon Glynn, David B Goldstein, Hongsheng Gui, Youling Guo, Kevin F Haas, Hakon Hakonarson, Kerstin Hallmann, Sheryl Haut, Erin L Heinzen, Ingo Helbig, Christian Hengsbach, Helle Hjalgrim, Michele Iacomino, Andrés Ingason, Michael R Johnson, Reetta Kälviäinen, Anne-Mari Kantanen, Dalia Kasperavičiūte, Dorothee Kasteleijn-Nolst Trenite, Heidi E Kirsch, Robert C Knowlton, Bobby P C Koeleman, Roland Krause, Martin Krenn, Wolfram S Kunz, Ruben Kuzniecky, Patrick Kwan, Dennis Lal, Yu-Lung Lau, Anna-Elina Lehesjoki, Holger Lerche, Costin Leu, Dick Lindhout, Warren D Lo, Iscia Lopes-Cendes, Daniel H Lowenstein, Alberto Malovini, Anthony G Marson, Thomas Mayer, Mark McCormack, James L Mills, Nasir Mirza, Martina Moerzinger, Rikke S Møller, Anne M Molloy, Hiltrud Muhle, Mark Newton, Ping-Wing Ng, Markus M Nöthen, Peter Nürnberg, Terence J O’Brien, Karen L Oliver, Aarno Palotie, Faith Pangilinan, Sarah Peter, Slavé Petrovski, Annapurna Poduri, Michael Privitera, Rodney Radtke, Sarah Rau, Philipp S Reif, Eva M Reinthaler, Felix Rosenow, Josemir W Sander, Thomas Sander, Theresa Scattergood, Steven C Schachter, Christoph J Schankin, Ingrid E Scheffer, Bettina Schmitz, Susanne Schoch, Pak C Sham, Jerry J Shih, Graeme J Sills, Sanjay M Sisodiya, Lisa Slattery, Alexander Smith, David F Smith, Michael C Smith, Philip E Smith, Anja C M Sonsma, Doug Speed, Michael R Sperling, Bernhard J Steinhoff, Ulrich Stephani, Remi Stevelink, Konstantin Strauch, Pasquale Striano, Hans Stroink, Rainer Surges, K Meng Tan, Liu Lin Thio, G Neil Thomas, Marian Todaro, Rossana Tozzi, Maria S Vari, Eileen P G Vining, Frank Visscher, Sarah von Spiczak, Nicole M Walley, Yvonne G Weber, Zhi Wei, Judith Weisenberg, Christopher D Whelan, Peter Widdess-Walsh, Markus Wolff, Stefan Wolking, Wanling Yang, Federico Zara, Fritz Zimprich

المساهمون: D., Schijven, R., Stevelink, M., Mccormack, W., van Rheenen, J. J., Luykx, B. P. C., Koeleman, J. H., Veldink, Shatunov, Aleksey, Mclaughlin, Russell L., van der Spek, Rick A. A., Iacoangeli, Alfredo, Kenna, Kevin P., van Eijk, Kristel R., Ticozzi, Nicola, Rogelj, Bori, Vrabec, Katarina, Ravnik-Glavač, Metka, Koritnik, Blaž, Zidar, Janez, Leonardis, Lea, Dolenc Grošelj, Leja, Millecamps, Stéphanie, Salachas, Françoi, Meininger, Vincent, de Carvalho, Mamede, Pinto, Susana, Gromicho, Marta, Pronto-Laborinho, Ana, Mora, Jesus S., Rojas-García, Ricardo, Polak, Meraida, Chandran, Siddharthan, Colville, Shuna, Swingler, Robert, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Orrell, Richard W., Pittman, Alan, Sidle, Katie, Fratta, Pietro, Malaspina, Andrea, Topp, Simon, Petri, Susanne, Abdulla, Susanna, Drepper, Carsten, Sendtner, Michael, Meyer, Thoma, Ophoff, Roel A., Staats, Kim A., Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, Van Deerlin, Vivianna M., Trojanowski, John Q., Elman, Lauren, Mccluskey, Leo, Nazli Basak, A., Meitinger, Thoma, Lichtner, Peter, Blagojevic-Radivojkov, Milena, Andres, Christian R., Bensimon, Gilbert, Landwehrmeyer, Bernhard, Brice, Alexi, Payan, Christine A. M., Saker-Delye, Safaa, Dürr, Alexandra, Wood, Nicholas W., Tittmann, Luka, Lieb, Wolfgang, Franke, Andre, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M., Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean-Françoi, Uitterlinden, Andre G., Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, Curtis, Charle, van der Kooi, Anneke J., Weber, Marku, Shaw, Christopher E., Smith, Bradley N., Sproviero, Daisy, Cereda, Cristina, Ceroni, Mauro, Diamanti, Luca, Del Bo, Roberto, Corti, Stefania, Comi, Giacomo P., D'Alfonso, Sandra, Corrado, Lucia, Bertolin, Cinzia, Sorarù, Gianni, Mazzini, Letizia, Pensato, Viviana, Gellera, Cinzia

مصطلحات موضوعية: ALS, Epilepsy, Genetic correlation, Amyotrophic Lateral Sclerosi, Gene Frequency, Human, Risk, Genetic Variation, Genome-Wide Association Study, Negative Results

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/32409253; info:eu-repo/semantics/altIdentifier/wos/WOS:000539467300016; volume:92; firstpage:153; numberofpages:8; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/11577/3443731; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85084453564

الاتاحة: http://hdl.handle.net/11577/3443731
https://doi.org/10.1016/j.neurobiolaging.2020.04.011

المؤلفون: Dick Lindhout

المصدر: Epilepsie, periodiek voor professionals. 19:19-21

مصطلحات موضوعية: medicine.medical_specialty, medicine, Onchocerciasis, medicine.disease, Psychiatry, Psychology, Nature versus nurture

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::6b055be5637c0a72eeb680ea26ae0cc2
https://doi.org/10.54160/epilepsie.11037

المؤلفون: Machiel Zwarts, Loretta van Iterson, Marieke Dekker, Dick Lindhout

المصدر: Epilepsie, periodiek voor professionals. 19:16-18

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c831fd0d3dbea8e909ca45cdcc5b541b
https://doi.org/10.54160/epilepsie.11038

المؤلفون: Roos Rodenburg, Loretta van Iterson, Yfke Huber-Mollema, Dick Lindhout, Frans J. Oort

المساهمون: Developmental Psychopathology (RICDE, FMG), Methods and Statistics (RICDE, FMG)

المصدر: Journal of Neurology
Journal of neurology, 267(6). D. Steinkopff-Verlag

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Levetiracetam, Antiepileptic drugs, Lamotrigine, Neuropsychological Tests, Neuropsychological assessment, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Cognition, Child Development, Pregnancy, medicine, Humans, Cognitive Dysfunction, 030212 general & internal medicine, Prospective Studies, Registries, Child, Wechsler Intelligence Scale for Children, Netherlands, Original Communication, medicine.diagnostic_test, business.industry, Valproic Acid, Wechsler Scales, Wechsler Adult Intelligence Scale, Carbamazepine, medicine.disease, Neurology, EURAP & development, Prenatal Exposure Delayed Effects, Anticonvulsants, Female, Neurology (clinical), business, Neurocognitive, 030217 neurology & neurosurgery, medicine.drug

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f5a03180fa8c2504aa389a0f796bf94
http://europepmc.org/articles/PMC7293688

المؤلفون: Mieke M. van Haelst, Emma de Haan, Eline A. Verberne, J. Peter van Tintelen, Dick Lindhout

المصدر: Reproductive Toxicology, 87, 125. Elsevier Inc.
Verberne, E A, de Haan, E, van Tintelen, J P, Lindhout, D & van Haelst, M M 2019, ' Fetal methotrexate syndrome: A systematic review of case reports ', Reproductive Toxicology, vol. 87, pp. 125-139 . https://doi.org/10.1016/j.reprotox.2019.05.066

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Microcephaly, 010501 environmental sciences, Toxicology, 01 natural sciences, Craniosynostosis, 03 medical and health sciences, Fetus, Pregnancy, medicine, Humans, Congenital anomaly, Syndactyly, 030304 developmental biology, 0105 earth and related environmental sciences, Tetralogy of Fallot, 0303 health sciences, business.industry, Pulmonary valve atresia, Abnormalities, Drug-Induced, Syndrome, medicine.disease, Teratogen, Teratology, Teratogens, Methotrexate, Antirheumatic Agents, embryonic structures, business, medicine.drug

وصف الملف: text/plain; image/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c6a00c331afc68a48bd80af98fbf298
https://doi.org/10.1016/j.reprotox.2019.05.066

المؤلفون: Dick Lindhout, Yfke Huber-Mollema, Roos Rodenburg, Frans J. Oort

المساهمون: Developmental Psychopathology (RICDE, FMG), Methods and Statistics (RICDE, FMG)

المصدر: Epilepsia, 60(6), 1069-1082. Wiley-Blackwell
Epilepsia

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Pediatrics, medicine.medical_specialty, Levetiracetam, Population, Mothers, Child Behavior Disorders, Lamotrigine, EURAP & Development, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Pregnancy, medicine, Humans, Prospective Studies, Registries, antiepileptic drugs, Child, Child Behavior Checklist, education, child development, education.field_of_study, behavior, business.industry, Valproic Acid, Social Behavior Disorders, Carbamazepine, medicine.disease, Child development, 030104 developmental biology, Neurology, Prenatal Exposure Delayed Effects, Full‐length Original Research, Anticonvulsants, Female, Neurology (clinical), teratogenicity, business, 030217 neurology & neurosurgery, medicine.drug

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b09244ab4a10f30d9184626620372d78
https://doi.org/10.1111/epi.15968

المؤلفون: Dick Lindhout, Bianca Berghuis, Bobby P. C. Koeleman, Janic Hulst, Gerrit-Jan de Haan, Josemir W. Sander, Anja C M Sonsma, Mark McCormack

المصدر: Epilepsia

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, Oxcarbazepine, Dizziness, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Internal medicine, medicine, Humans, sodium levels, Adverse effect, Fatigue, Retrospective Studies, Diplopia, anti‐seizure medication, business.industry, Sodium, nutritional and metabolic diseases, drug treatment, Carbamazepine, Odds ratio, Middle Aged, medicine.disease, 030104 developmental biology, Neurology, Concomitant, Full‐length Original Research, adverse effects, Anticonvulsants, Female, Neurology (clinical), medicine.symptom, business, Hyponatremia, 030217 neurology & neurosurgery, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab918f6439c18a358bd63b49b738658e
https://pubmed.ncbi.nlm.nih.gov/33576502

المؤلفون: Yfke Huber-Mollema, Frans J. Oort, Roos Rodenburg, Dick Lindhout

المساهمون: Developmental Psychopathology (RICDE, FMG), Methods and Statistics (RICDE, FMG)

المصدر: Epilepsy & Behavior, 105:106966. Academic Press Inc.

مصطلحات موضوعية: Adult, Male, Mothers, Child Behavior Disorders, 03 medical and health sciences, Behavioral Neuroscience, Epilepsy, 0302 clinical medicine, Quality of life (healthcare), Child of Impaired Parents, Pregnancy, Humans, Medicine, 030212 general & internal medicine, Child, Netherlands, Problem Behavior, business.industry, medicine.disease, Child development, Mother-Child Relations, Family life, Neurology, Well-being, Quality of Life, Anticonvulsants, Female, Observational study, Neurology (clinical), business, Psychosocial, 030217 neurology & neurosurgery, Clinical psychology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51dd4d1c2aff6a641c14ee7807a9924e
https://dare.uva.nl/personal/pure/en/publications/wellbeing-of-mothers-with-epilepsy-with-schoolaged-children(905753d1-e189-49de-aed9-8b31c4794b83).html

المؤلفون: Birgitte Forsom Sondal, Zarouhi Hertz, Brenda Diputado, Meritxell Martinez Ferri, Odo Hildenhagen, Aldo Paggi, Gerhard Luef, Jakob Christensen, John Craig, Jana Zárubová, Gordana Kiteva-Trencevska, Raffaele Rocchi, Erik Tauboll, Lisa Gordon, Terttu Heikinheimo-Connell, Uden Navn, Ketevan Khomeriki, Iva Marečková, Erminio Bonizzoni, Michela Cecconi, Lone Rodam, Astrid Carius, Ineke Hogenesch, Katarzyna Miesczanleh, Angelo Labate, Eva Kumlien, Claus Albretsen, Torbjörn Tomson, Chiara Pantaleoni, David Sopelana Garay, Albertina Franza, Imad Halawa, Stefan Juhl, Emilio Perucca, Pia Gellert, Daniela Marino, Aline Russell, E. Kluck, Eylert Brodtkorb, Luigi Maria Specchio, Isabel Pires, Pietro Pignatta, Frank J.E. Vajda, Anette Huuse Farmen, Hans Lindsten, Boštjan Čebular, Maria Paola Canevini, Jens Arentsen, Francesca Faravelli, Bettina Schmitz, Noémi Becser Andersen, Birgit Müffelmann, Petr Bušek, T.-Y. Chang, Alma Sikiric, Judith Osseforth, Elias Zakharia, Elsebeth Bruun Christensen, Gemma Sansa Fayos, Vaiva Petrenaite, Alessandra Pistelli, Eliana Pastor, Hana Krijtová, Tim Hendgen, Leonor Cabral-Lim, Marina Trivisano, Hsiang-Yu Yu, Renata Listonova, Torleiv Svendsen, Vladimír Safcák, Nicoletta Foschi, Kristina Malmgren, Reetta Kälviäinen, Dag Aurlien, Martin J. Brodie, Maria Dolores Castro Vilanova, Anders Nilsson, Jesús Antonio Riuz Gimenez, Christian Samsonsen, Katsuyuki Fukushima, Maria Strandberg, Masaaki Kato, Giovanni De Maria, Katrine Haggag, Anna Maija Saukkonen, Maja Milovanovic, Masahiro Mizobuchi, Peter Mattsson, Bernhard Oehl, Anne Sabers, Juan Luis Becerra Cuñat, Mogens Worm, Antonio Gambardella, Miri Neufeld, Reina Roivainen, Kiyohito Terada, Janne Marit Ertresvåg, Birthe Pedersen, Gisela Rytířová, Claudia Cagnetti, Sanjeev V Thomas, Dick Lindhout, Silvia Kochen, Katherine Turner, Dieter Dennig, Luisa Antonini, Dina Battino, Laura Broglio, Aileen McGonigal, Helena Gauffin, Andrea Ortenzi, Ismael Barzinji, Hideyuki Ohtani, Rasmus Lossius, Elisabeth Robert-Gnansia, Morteza Zarifi-Oskoie, Leif Gjerstad, Barbara Tettenborn, Stephanie Hödl, Martin Kurthen, Barbara Mostacci, Alejandro De Marinis, Natalia Bohorquez Morera, Karl O. Nakken, Yushi Inoue, Germaine Kenou Van Rijckevorssel, Theresa Lasch, Iñigo Garamendi Ruiz, Silje Alvestad, Eugène van Puijenbroek, Anders Lundgren, Elena Zambrelli, Toni Escartin, Bernhard J. Steinhoff, Dominique Flügel

المساهمون: PharmacoTherapy, -Epidemiology and -Economics, Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET), Tomson T, Battino D, Bonizzoni E, Craig J, Lindhout D, Perucca E, Sabers A, Thomas SV, Vajda F, EURAP Study Group, Bisulli F, Tinuper P

المصدر: Lancet Neurology, 17(6), 530-538. ELSEVIER SCIENCE INC
Christensen, J, Brændgaard, H & EURAP Study Group 2018, ' Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry ', Lancet Neurology, vol. 17, no. 6, pp. 530-538 . https://doi.org/10.1016/S1474-4422(18)30107-8
Epilepsy Currents
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET

مصطلحات موضوعية: Pediatrics, congenital heart malformation, topiramate, anticonvulsive agent, oxcarbazepine, Current Literature in Clinical Science, phenobarbital, cleft lip, neural tube defect, Epilepsy, 0302 clinical medicine, newborn, purl.org/becyt/ford/3.2 [https], fetus outcome, 030212 general & internal medicine, Prospective cohort study, Oxcarbazepine, anticonvulsant therapy, cleft palate, adult, phenytoin, article, longitudinal study, Abnormalities, Drug-Induced, polydactyly, cohort analysis, Kerala, fetus, female, priority journal, carbamazepine, monotherapy, perinatal death, purl.org/becyt/ford/3 [https], Anticonvulsants, Levetiracetam, lamotrigine, pregnancy, medicine.drug, Cohort study, prospective study, Topiramate, medicine.medical_specialty, levetiracetam, congenital malformation, prevalence, first trimester pregnancy, prenatal drug exposure, Lamotrigine, pregnancy termination, live birth, kidney malformation, TERATOGENICIDAD, Young Adult, 03 medical and health sciences, male, valproic acid, medicine, Humans, fetus disease, follow up, human, hypospadias, Dose-Response Relationship, Drug, business.industry, EPILEPSIA, Australia, EMBARAZO, multiple malformation syndrome, Carbamazepine, gastrointestinal malformation, medicine.disease, major clinical study, United Kingdom, Pregnancy Complications, Logistic Models, pregnant woman, maternal age, epilepsy, Neurology (clinical), conception, teratogenicity, business, Ireland, 030217 neurology & neurosurgery

وصف الملف: application/pdf; STAMPA; application/vnd.openxmlformats-officedocument.wordprocessingml.document

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::065767073528c3f34f5392a2c910cf73
https://research.rug.nl/en/publications/e1ac6454-26ab-449f-b9d3-ded61fad6250

المؤلفون: Dalila Pinto, Birgit Westl, Gerrit-jan De Haan, Gabrielle Rudolf, Berta Martins Da, Edouard Hirsch, Dick Lindhout, Dorothée G. A, Kasteleijn-nolst Trenité, Bobby P. C

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://hmg.oxfordjournals.org/content/early/2004/11/17/hmg.ddi018.full.pdf.

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.613.2485; http://hmg.oxfordjournals.org/content/early/2004/11/17/hmg.ddi018.full.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.613.2485
http://hmg.oxfordjournals.org/content/early/2004/11/17/hmg.ddi018.full.pdf

المؤلفون: John Craig, Sanjeev V Thomas, Erminio Bonizzoni, Frank J.E. Vajda, Anne Sabers, Dina Battino, Dick Lindhout, Torbjörn Tomson, Emilio Perucca

المصدر: Epilepsy Res

مصطلحات موضوعية: Adult, Risk, medicine.medical_specialty, Vagus Nerve Stimulation, Offspring, medicine.medical_treatment, Article, Cohort Studies, Young Adult, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Pregnancy, medicine, Humans, Registries, Young adult, Fetus, 030219 obstetrics & reproductive medicine, business.industry, Obstetrics, Infant, Newborn, Pregnancy Outcome, Glaucoma, medicine.disease, Combined Modality Therapy, Confidence interval, Pregnancy Complications, Neurology, Teratogenesis, Anticonvulsants, Female, Neurology (clinical), business, 030217 neurology & neurosurgery, Vagus nerve stimulation, Cohort study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe2bd175694c6bf15a350de588725e04
https://doi.org/10.1016/j.eplepsyres.2017.05.013

المؤلفون: Marjon Van Slegtenhorst, Senno Verhoef, Anita Tempelaars, Lida Bakker, Qi Wang, Marja Wessels, Remco Bakker, Mark Nellist, Dick Lindhout, Dicky Halley, Van Den Ouweland, J. Med Genet, Email Alerting, J Med Genet, A Verhoef, A Tempelaars, L Bakker, Q Wang, M Wessels, R Bakker, M Nellist, D Lindhout, D Halley

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://repub.eur.nl/res/pub/9088/10227394.pdf.

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.324.9333; http://repub.eur.nl/res/pub/9088/10227394.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.324.9333
http://repub.eur.nl/res/pub/9088/10227394.pdf

المؤلفون: Jacques L. Michaud, Jessica Sebastian, Hanrong Wu, Dick Lindhout, Karla Manzano-Vargas, Nuwan C. Hettige, Ingrid M. Wentzensen, Huashan Peng, Amy Crunk, Heika Silviera, Malvin Jefri, Henry Houlden, Fadi F. Hamdan, Zahia Aouabed, Stephanie Efthymiou, Xin Zhang, Renske Oegema, Arnaud Tanti, Jerry Vockley, Gustavo Turecki, Julien van Gils, Amber G. Begtrup, Christina Nassif, Gunnar Houge, Naomichi Matsumoto, Thomas Bourgeron, Jean-François Théroux, Emily Fassi, Noriko Miyake, Robert D. Nicholls, Jose E. Martinez, Kristin Herman, Lilit Antonyan, Philippe M. Campeau, Margaret G. Au, Dominic Nelson, Vincenzo Salpietro, Scott C. Bell, Pierre Priam, Joshua L. Deignan, Gregory M. Cooper, Rune Østern, Han G. Brunner, Dagmar Huhle, Amy Goldstein, John M. Graham, Christine Coubes, Koen L.I. van Gassen, Tabib Dabir, Maria Hafström, Simon Gravel, Sophie Ehresmann, Elsa Rossignol, Ilaria Kolobova, Walla Al-Hertani, Julie A. Lessard, Lionel Carmant, Sonja Martin, Richard Delorme, Carl Ernst, Jolien S. Klein Wassink-Ruiter, Naguib Mechawar, Yoshio Makita, Candice R. Finnila, Rami Abou Jamra, Anne Lortie, Justine Rousseau, Sarju G. Mehta, Lina Ghaloul-Gonzalez

المساهمون: MUMC+: DA Klinische Genetica (5), Klinische Genetica, RS: GROW - R4 - Reproductive and Perinatal Medicine, McGill University = Université McGill [Montréal, Canada], Université de Montréal (UdeM), University of Pittsburgh (PITT), Pennsylvania Commonwealth System of Higher Education (PCSHE), GeneDx [Gaithersburg, MD, USA], University of California [Davis] (UC Davis), University of California, David Geffen School of Medicine [Los Angeles], University of California [Los Angeles] (UCLA), University of California-University of California, University of Calgary, UCL, Institute of Neurology [London], Yokohama City University (YCU), Asahikawa Medical College, Trondheim University, Haukeland University Hospital, University of Bergen (UiB), Washington University School of Medicine in St. Louis, Washington University in Saint Louis (WUSTL), University of Groningen [Groningen], University Medical Center Groningen [Groningen] (UMCG), Children's Hospital of Pittsburgh of UPMC [Etats-Unis], Belfast City Hospital, Génétique humaine et fonctions cognitives - Human Genetics and Cognitive Functions (GHFC (UMR_3571 / U-Pasteur_1)), Institut Pasteur [Paris]-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Child and Adolescent Psychiatry Department [AP- HP Hôpital Robert Debré], AP-HP Hôpital universitaire Robert-Debré [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), HudsonAlpha Institute for Biotechnology [Huntsville, AL], Children’s Rehabilitation Service [Mobile, AL] (CRS), Children's Rehabilitation Service [Montgomery, AL] (CRS), University Medical Center [Utrecht], Cambridge University Hospitals - NHS (CUH), University of Cambridge [UK] (CAM), University Hospital Leipzig, Donders Institute for Brain, Cognition and Behaviour, Radboud university [Nijmegen], Maastricht University Medical Centre (MUMC), Maastricht University [Maastricht], Cedars-Sinai Medical Center, CHU Montpellier, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), We acknowledge funding by FRQS doctoral (S.B.), Indonesian Endowment Fund for Education PhD award (M.J.), CONACYT (Mexico) and MITACS (K.M.V.), Genome Canada and Génome Québec (J.L.M. and E.R.), Canada Research Chairs program (G.T. and C.E.), AMED, MEXT, JST, MHLW, and Takeda Science Foundation (N. Matsumoto), and CIHR grant (C.E. and P.M.C.)., University of California (UC), University of California (UC)-University of California (UC), Institut Pasteur [Paris] (IP)-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Radboud University [Nijmegen], Faculteit Medische Wetenschappen/UMCG

المصدر: American Journal of Human Genetics, 104, 5, pp. 815-834
American Journal of Human Genetics, 104(5), 815. Cell Press
American Journal of Human Genetics, 104(5), 815-834. Cell Press
American Journal of Human Genetics, 104, 815-834
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2019, 104 (5), pp.815-834. ⟨10.1016/j.ajhg.2019.03.022⟩
American Journal of Human Genetics, 2019, 104 (5), pp.815-834. ⟨10.1016/j.ajhg.2019.03.022⟩
American Journal of Human Genetics, 104(5), 815-834. CELL PRESS

مصطلحات موضوعية: 0301 basic medicine, Male, PROTEIN EXPRESSION, Chromosomal Proteins, Non-Histone, Mutant, MESH: Neurons, 0302 clinical medicine, SYNAPTIC PLASTICITY, MESH: Child, Genetics(clinical), Global developmental delay, TRANSCRIPTION, Child, Genetics (clinical), ACTL6B, genetic engineering, intellectual disability, neurodevelopment, seizure, stem cells, Genetics, Neurons, SWI/SNF COMPLEX, MESH: Infant, Hypotonia, Neural stem cell, Chromatin, DNA-Binding Proteins, medicine.anatomical_structure, MESH: Young Adult, MESH: Epilepsy, Child, Preschool, Female, medicine.symptom, Adult, MESH: Mutation, DISORDERS, Induced Pluripotent Stem Cells, Biology, MESH: Induced Pluripotent Stem Cells, MESH: Actins, MESH: Dendrites, Chromatin remodeling, Article, MESH: Chromatin, 03 medical and health sciences, Young Adult, All institutes and research themes of the Radboud University Medical Center, MESH: Chromosomal Proteins, Non-Histone, medicine, Journal Article, Humans, CHROMATIN REMODELING COMPLEX, Progenitor cell, Loss function, MESH: Neurodevelopmental Disorders, MESH: Humans, Epilepsy, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], [SCCO.NEUR]Cognitive science/Neuroscience, MESH: Child, Preschool, COFFIN-SIRIS SYNDROME, MEMORY, Infant, MESH: Adult, Dendrites, GENE, MESH: Male, Actins, 030104 developmental biology, Neurodevelopmental Disorders, Mutation, OLIGODENDROCYTE, Neuron, MESH: Female, 030217 neurology & neurosurgery, MESH: DNA-Binding Proteins

وصف الملف: image/pdf; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd69a3db8e881fea7dc94ed364dafd6d
https://hdl.handle.net/2066/203584

المؤلفون: Christian E. Elger, Wolfgang Lieb, Claudia B. Catarino, Pasquale Striano, Andreja Avbersek, Daniel H. Lowenstein, Philip E. M. Smith, G. Neil Thomas, Dick Lindhout, Erin L. Heinzen, Sanjay M. Sisodiya, Orrin Devinsky, Alexander R. H. Smith, Rainer Surges, Stefan Wolking, Patrick Cossette, Annapurna Poduri, Eric B. Geller, Stacey S. Cherny, Maria Stella Vari, Peter De Jonghe, Kevin Haas, Andres Ingason, Reetta Kälviäinen, Krishna Chinthapalli, Dennis Lal, Graeme J. Sills, Martina Moerzinger, Jonathan P. Bradfield, Mark R Newton, Federico Zara, Sheryl R. Haut, Warren D. Lo, Holger Lerche, Felix Rosenow, Robert C. Knowlton, Mark McCormack, Sarah Rau, Felicitas Becker, Andre Franke, Heidi E. Kirsch, Patrick Kwan, Remi Stevelink, Rodney A. Radtke, Michele Iacomino, Faith Pangilinan, Ulrich Stephani, David F. Smith, Eva M. Reinthaler, Chantal Depondt, Hiltrud Muhle, Russell J. Buono, Alison J. Coffey, Ellen Campbell, Marvin Johnson, Bernhard J. Steinhoff, Sarah von Spiczak, Yvonne G. Weber, Ping-Wing Ng, Kerstin Hallmann, Philipp S. Reif, David Goldstein, Bettina Schmitz, Antonietta Coppola, Jerry J. Shih, Karen Oliver, Anne-Mari Kantanen, Rossana Tozzi, Markus Wolff, Albert J. Becker, Anne M. Molloy, Lisa Slattery, James L. Mills, Judith L.Z. Weisenberg, Jacqueline A. French, Lawrence C. Brody, Int League Against Epilepsy Conso, Peter Widdess-Walsh, Helle Hjalgrim, Christian Hengsbach, Christoph J. Schankin, Johan G. Eriksson, Tracy A. Glauser, Yu-Lung Lau, Larry Baum, Anna-Elina Lehesjoki, Nicole M. Walley, Josemir W. Sander, Markus M. Noethen, Simon Glynn, Jennifer Jamnadas-Khoda, Thomas Bast, Susanne Schoch, Iscia Lopes-Cendes, Doug Speed, Anja C M Sonsma, John Craig, Ingo Helbig, Marian Todaro, Gregory D. Cascino, Steven C. Schachter, Fritz Zimprich, Samuel F. Berkovic, Michael Privitera, Ben Francis, Martin Krenn, Rikke S. Møller, Eileen P.G. Vining, Martha Feucht, Bobby P. C. Koeleman, Ruben Kuzniecky, Christian Gieger, K. Meng Tan, Dalia Kasperaviciute, Pauls Auce, Gianpiero L. Cavalleri, Melanie Bahlo, Zhi Wei, Nasir Mirza, David J. Balding, Mike Smith, Liu Lin Thio, Alastair Compston, Katja E. Boysen, Gerrit-Jan de Haan, Hongsheng Gui, Hakon Hakonarson, Christopher D. Whelan, Colin P. Doherty, Youling Guo, Aarno Palotie, Wolfram S. Kunz, Slavé Petrovski, Thomas Sander, Frank Visscher, Bianca Berghuis, Costin Leu, Verena Gaus, Dennis J. Dlugos, Ingrid E. Scheffer, Alberto Malovini, Konstantin Strauch, Wanling Yang, Saskia Freytag, H. Stroink, Pak C. Sham, Norman Delanty, Terence J. O'Brien, Carolien G.F. de Kovel, Thomas U. Mayer, Anthony G Marson, Bassel Abou-Khalil, Thomas N. Ferraro, Dorothée G.A. Kasteleijn-Nolst Trenité, Roland Krause, Sarah Peter, Peter Nuernberg, Theresa Scattergood, Michael R. Sperling

المساهمون: Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Clinicum, Department of Medical and Clinical Genetics, Medicum, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders, Int League Against Epilepsy Conso, Abou-Khalil, Bassel, Auce, Paul, Avbersek, Andreja, Bahlo, Melanie, J Balding, David, Bast, Thoma, Baum, Larry, J Becker, Albert, Becker, Felicita, Berghuis, Bianca, F Berkovic, Samuel, E Boysen, Katja, P Bradfield, Jonathan, C Brody, Lawrence, J Buono, Russell, Campbell, Ellen, D Cascino, Gregory, B Catarino, Claudia, L Cavalleri, Gianpiero, S Cherny, Stacey, Chinthapalli, Krishna, J Coffey, Alison, Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, J Craig, John, de Haan, Gerrit-Jan, De Jonghe, Peter, F de Kovel, Carolien G, Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, J Dlugos, Denni, P Doherty, Colin, E Elger, Christian, G Eriksson, Johan, N Ferraro, Thoma, Feucht, Martha, Francis, Ben, Franke, Andre, A French, Jacqueline, Freytag, Saskia, Gaus, Verena, B Geller, Eric, Gieger, Christian, Glauser, Tracy, Glynn, Simon, B Goldstein, David, Gui, Hongsheng, Guo, Youling, F Haas, Kevin, Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, L Heinzen, Erin, Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, André, Jamnadas-Khoda, Jennifer, R Johnson, Michael, Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, E Kirsch, Heidi, C Knowlton, Robert, C Koeleman, Bobby P, Krause, Roland, Krenn, Martin, S Kunz, Wolfram, Kuzniecky, Ruben, Kwan, Patrick, Lal, Denni, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, D Lo, Warren, Lopes-Cendes, Iscia, H Lowenstein, Daniel, Malovini, Alberto, G Marson, Anthony, Mayer, Thoma, Mccormack, Mark, L Mills, Jame, Mirza, Nasir, Moerzinger, Martina, S Møller, Rikke, M Molloy, Anne, Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, M Nöthen, Marku, Nürnberg, Peter, J O'Brien, Terence, L Oliver, Karen, Palotie, Aarno, Pangilinan, Faith, Peter, Sarah, Petrovski, Slavé, Poduri, Annapurna, Privitera, Michael, Radtke, Rodney, Rau, Sarah, S Reif, Philipp, M Reinthaler, Eva, Rosenow, Felix, W Sander, Josemir, Sander, Thoma, Scattergood, Theresa, C Schachter, Steven, J Schankin, Christoph, E Scheffer, Ingrid, Schmitz, Bettina, Schoch, Susanne, C Sham, Pak, J Shih, Jerry, J Sills, Graeme, M Sisodiya, Sanjay, Slattery, Lisa, Smith, Alexander, F Smith, David, C Smith, Michael, E Smith, Philip, M Sonsma, Anja C, Speed, Doug, R Sperling, Michael, J Steinhoff, Bernhard, Stephani, Ulrich, Stevelink, Remi, Strauch, Konstantin, Striano, Pasquale, Stroink, Han, Surges, Rainer, Meng Tan, K, Lin Thio, Liu, Neil Thomas, G, Todaro, Marian, Tozzi, Rossana, S Vari, Maria, G Vining, Eileen P, Visscher, Frank, von Spiczak, Sarah, M Walley, Nicole, G Weber, Yvonne, Wei, Zhi, Weisenberg, Judith, D Whelan, Christopher, Widdess-Walsh, Peter, Wolff, Marku, Wolking, Stefan, Yang, Wanling, Zara, Federico, Zimprich, Fritz, Wellcome Trust, GlaxoSmithKline Services Unlimited, Commission of the European Communities, Medical Research Council (MRC), Imperial College Healthcare NHS Trust- BRC Funding

المصدر: Nature Communications. London, United Kingdom: Nature Publishing Group (2018).
Nature communications, vol 9, iss 1
Hjalgrim, H, Møller, R S & The International League Against Epilepsy Consortium on Complex Epilepsies 2018, ' Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies ', Nature Communications, vol. 9, 5269 . https://doi.org/10.1038/s41467-018-07524-z
Nature Communications, Vol 9, Iss 1, Pp 1-15 (2018)
Nature Communications
Nature communications
The International League Against Epilepsy Consortium on Complex Epilepsies 2018, ' Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies ', Nature Communications, vol. 9, no. 1, 5269 . https://doi.org/10.1038/s41467-018-07524-z
Nature communications, 9 (1
Nat. Commun. 9:5269 (2018)
The International League Against Epilepsy, Consortium on Complex (2018). Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Nature communications, 9(1), p. 5269. Springer Nature 10.1038/s41467-018-07524-z <http://dx.doi.org/10.1038/s41467-018-07524-z>

مصطلحات موضوعية: 0301 basic medicine, Linkage disequilibrium, LD SCORE REGRESSION, Neurology [D14] [Human health sciences], General Physics and Astronomy, Genome-wide association study, ILAE COMMISSION, Neurodegenerative, Genome, Linkage Disequilibrium, Epilepsy, Gene Frequency, Missing heritability problem, 2.1 Biological and endogenous factors, Aetiology, lcsh:Science, International League Against Epilepsy Consortium on Complex Epilepsies, Multidisciplinary, Genetic Predisposition to Disease/genetics, Chromosome Mapping, ASSOCIATION, Epilepsy/classification, Single Nucleotide, ABSENCE, 3. Good health, Technologie de l'environnement, contrôle de la pollution, SNP HERITABILITY, Neurological, Genome-Wide Association Study/methods, Case-Control Studie, Engineering sciences. Technology, Human, Biotechnology, EXPRESSION, SUSCEPTIBILITY LOCI, Genotype, Science, Quantitative Trait Loci, 610 Medicine & health, Computational biology, Biology, Quantitative trait locus, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Article, GENETIC ARCHITECTURE, 03 medical and health sciences, MD Multidisciplinary, medicine, Genetics, SNP, Chimie, FRONTAL-LOBE, Humans, Genetic Predisposition to Disease, Polymorphism, METAANALYSIS, Neurologie [D14] [Sciences de la santé humaine], Physique, Human Genome, Neurosciences, General Chemistry, Astronomie, medicine.disease, Genetic architecture, Brain Disorders, 030104 developmental biology, Gene Expression Regulation, Case-Control Studies, epilepsy, lcsh:Q, 3111 Biomedicine, Quantitative Trait Loci/genetics, Genome-Wide Association Study

وصف الملف: application/pdf; pdf; 1 full-text file(s): application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7b607d077bc96797c19615b63305779
http://orbilu.uni.lu/handle/10993/37681

المؤلفون: Dick Lindhout, Frans J. Oort, Loretta van Iterson, Josemir W. Sander, Yfke Huber-Mollema, Roos Rodenburg

المصدر: Epilepsybehavior : EB. 86

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Mothers, PsycINFO, Behavioral neuroscience, 03 medical and health sciences, Behavioral Neuroscience, Epilepsy, 0302 clinical medicine, Child Development, Pregnancy, medicine, Humans, 0501 psychology and cognitive sciences, Psychiatry, Child, Family Health, Parenting, business.industry, Clinical study design, 05 social sciences, Pregnancy Outcome, medicine.disease, Child development, Pregnancy Complications, Observational Studies as Topic, Neurology, Prenatal Exposure Delayed Effects, Anticonvulsants, Female, Neurology (clinical), Drugs in pregnancy, business, Neurocognitive, 030217 neurology & neurosurgery, 050104 developmental & child psychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8bd83cdc60a789632c77f3bb304f61c
https://pubmed.ncbi.nlm.nih.gov/30030084

المؤلفون: Ragna S, Boerma, Kees P, Braun, Marcel P H, van den Broek, Maarten P H, van de Broek, Frederique M C, van Berkestijn, Marielle E, Swinkels, Eveline O, Hagebeuk, Dick, Lindhout, Marjan, van Kempen, Maartje, Boon, Joost, Nicolai, Carolien G, de Kovel, Eva H, Brilstra, Bobby P C, Koeleman

المساهمون: Klinische Neurowetenschappen, MUMC+: MA Med Staf Spec Neurologie (9)

المصدر: Neurotherapeutics
Neurotherapeutics, 13(1), 192. Springer New York
Neurotherapeutics, 13(1), 192-197. SPRINGER
Neurotherapeutics, 13(1), 192-197. Springer Verlag

مصطلحات موضوعية: 0301 basic medicine, Phenytoin, Male, medicine.medical_specialty, SCN8A, Neurology, Encephalopathy, Mutation, Missense, Clinical Neurology, Nerve Tissue Proteins, Pharmacology, medicine.disease_cause, PATIENT, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Sodium channel blocker, medicine, Missense mutation, Humans, Pharmacology (medical), Precision Medicine, Child, MUTATION, Mutation, Brain Diseases, business.industry, Sodium channel, phenytoin, ENCEPHALOPATHY, medicine.disease, 030104 developmental biology, Treatment Outcome, epileptic encephalopathy, NAV1.6 Voltage-Gated Sodium Channel, sodium channel blockers, Child, Preschool, Commentary, Anticonvulsants, Female, Original Article, Neurology (clinical), business, 030217 neurology & neurosurgery, medicine.drug

وصف الملف: image/pdf; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fff71235a7be2aaf8e77e9be8eaa4c1d
http://europepmc.org/articles/PMC4720675

المؤلفون: Elly F. Ippel, Huibert H. Geesink, Bobby P. C. Koeleman, Jeanet M. Kemmeren, Oebele F. Brouwer, Anton de Louw, Paul B. Augustijn, W. Boudewijn Gunning, Eveline E. O. Hagebeuk, Patricia E. Vermeer-de Bondt, Nienke E. Verbeek, Floor E. Jansen, Kees P.J. Braun, Jolanda H. Schieving, Eva H. Brilstra, Nine V A M Knoers, Hans Stroink, Marjan J. A. van Kempen, Rinze F. Neuteboom, Nicoline A.T. van der Maas, Dick Lindhout, Anja C M Sonsma, R. Jeroen Vermeulen, Joost Nicolai, Carolien G.F. de Kovel

المساهمون: Pediatric surgery, NCA - Brain mechanisms in health and disease, Medical Informatics, Erasmus MC other, Neurology, Clinical Genetics, Child and Adolescent Psychiatry / Psychology

المصدر: Neurology, 85(7), 596-603. LIPPINCOTT WILLIAMS & WILKINS
Verbeek, N E, van der Maas, N A T, Sonsma, A C M, Ippel, E, Bondt, P E V D, Hagebeuk, E, Jansen, F E, Geesink, H H, Braun, K P, de Louw, A, Augustijn, P B, Neuteboom, R F, Schieving, J H, Stroink, H, Vermeulen, R J, Nicolai, J, Brouwer, O F, van Kempen, M, de Kovel, C G F, Kemmeren, J M, Koeleman, B P C, Knoers, N V, Lindhout, D, Gunning, W B & Brilstra, E H 2015, ' Effect of vaccinations on seizure risk and disease course in Dravet syndrome ', Neurology, vol. 85, no. 7, pp. 596-603 . https://doi.org/10.1212/WNL.0000000000001855
Neurology, 85(7), 596-603. Lippincott Williams and Wilkins
Neurology, 85(7), 596-603. Lippincott Williams & Wilkins

مصطلحات موضوعية: Adult, Male, Risk, WHOLE-CELL PERTUSSIS, Pediatrics, medicine.medical_specialty, Adolescent, VACCINE, Epilepsies, Myoclonic, Diphtheria-Tetanus-acellular Pertussis Vaccines, CONTROLLED-TRIAL, MEASLES, Rate ratio, Rubella, Measles, Young Adult, Epilepsy, SDG 3 - Good Health and Well-being, Dravet syndrome, Seizures, medicine, Humans, SCN1A, Age of Onset, Child, Diphtheria-Tetanus-Pertussis Vaccine, EPILEPSY, Retrospective Studies, FEBRILE SEIZURES, business.industry, Incidence, Vaccination, Infant, ENCEPHALOPATHY, Odds ratio, MUMPS, medicine.disease, NAV1.1 Voltage-Gated Sodium Channel, ACELLULAR PERTUSSIS, Child, Preschool, Disease Progression, Female, Neurology (clinical), Age of onset, business, Measles-Mumps-Rubella Vaccine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2509593c12bd74b624411a19ee6674b7
https://doi.org/10.1212/wnl.0000000000001855

المؤلفون: Grazia M.S. Mancini, Cacha M.P.C.D. Peeters-Scholte, Paul B. Augustijn, Dick Lindhout, Eva H. Brilstra, A I Kistemaker, M.J.A. van Kempen, H A Newman, Oebele F. Brouwer, Katherine L. Helbig, Rinze F. Neuteboom, Marjolein Kriek, Bobby P. C. Koeleman, Patrick Rump, Yvonne J. Vos, I M de Lange, K. Hodges, Nine V A M Knoers

المساهمون: Neurology, Clinical Genetics

المصدر: Neurogenetics, 18(3), 147-153. SPRINGER
neurogenetics, 18(3), 147-153
Neurogenetics
Neurogenetics, 18(3), 147. Springer Verlag
Neurogenetics, 18(3), 147-153. Springer-Verlag

مصطلحات موضوعية: 0301 basic medicine, Male, DISORDER, Pediatrics, PCDH19, Intellectual disability, Disease, DE-NOVO, Epilepsy, 0302 clinical medicine, Genetics (clinical), Genetics, PCDH19-RELATED EPILEPSY, medicine.diagnostic_test, Mosaicism, Medical record, High-Throughput Nucleotide Sequencing, ENCEPHALOPATHY, Cadherins, Phenotype, PROTOCADHERIN 19 MUTATIONS, Female, Original Article, medicine.medical_specialty, Heterozygote, Encephalopathy, 03 medical and health sciences, Cellular and Molecular Neuroscience, Sex Factors, Seizures, medicine, Journal Article, Humans, Genetic Predisposition to Disease, Genetic testing, SPECTRUM, business.industry, GENE-RELATED EPILEPSY, medicine.disease, FEMALE-LIMITED EPILEPSY, Human genetics, Protocadherins, 030104 developmental biology, Mutation, business, 030217 neurology & neurosurgery, MENTAL-RETARDATION

وصف الملف: application/pdf; image/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a554e3716d9f3a84abb0166073ce0be3
https://research.rug.nl/en/publications/3dd56f82-3354-47f4-b279-a897bf99d84e