Application of the 2017 Revised McDonald Criteria for Multiple Sclerosis to Patients With a Typical Clinically Isolated Syndrome
van der Vuurst de Vries, Roos M, Mescheriakova, Julia Y, Wong, Yu Yi M, Runia, Tessel F, Jafari, Naghmeh, Samijn, Johnny P, de Beukelaar, Janet W K, Wokke, Beatrijs H A, Siepman, Theodora A M, Hintzen, Rogier Q
Published in JAMA neurology (01.11.2018)
Published in JAMA neurology (01.11.2018)
Get more information
Journal Article
Soluble CD27 Levels in Cerebrospinal Fluid as a Prognostic Biomarker in Clinically Isolated Syndrome
van der Vuurst de Vries, Roos M, Mescheriakova, Julia Y, Runia, Tessel F, Jafari, Naghmeh, Siepman, Theodora A M, Hintzen, Rogier Q
Published in JAMA neurology (01.03.2017)
Published in JAMA neurology (01.03.2017)
Get more information
Journal Article
Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family
Mescheriakova, Julia Y, Verkerk, Annemieke JMH, Amin, Najaf, Uitterlinden, André G, van Duijn, Cornelia M, Hintzen, Rogier Q
Published in Multiple sclerosis (01.06.2019)
Published in Multiple sclerosis (01.06.2019)
Get full text
Journal Article
High neurofilament levels are associated with clinically definite multiple sclerosis in children and adults with clinically isolated syndrome
van der Vuurst de Vries, Roos M, Wong, Yu Yi M, Mescheriakova, Julia Y, van Pelt, E Daniëlle, Runia, Tessel F, Jafari, Naghmeh, Siepman, Theodora AM, Melief, Marie-José, Wierenga-Wolf, Annet F, van Luijn, Marvin M, Samijn, Johnny P, Neuteboom, Rinze F, Hintzen, Rogier Q
Published in Multiple sclerosis (01.06.2019)
Published in Multiple sclerosis (01.06.2019)
Get full text
Journal Article
Smoking at time of CIS increases the risk of clinically definite multiple sclerosis
van der Vuurst de Vries, Roos M., Mescheriakova, Julia Y., Runia, Tessel F., Siepman, Theodora A. M., Wokke, Beatrijs H. A., Samijn, Johnny P. A., Hintzen, Rogier Q.
Published in Journal of neurology (01.05.2018)
Published in Journal of neurology (01.05.2018)
Get full text
Journal Article
Risk genes associated with pediatric-onset MS but not with monophasic acquired CNS demyelination
van Pelt, E Daniëlle, Mescheriakova, Julia Y, Makhani, Nalia, Ketelslegers, Immy A, Neuteboom, Rinze F, Kundu, Suman, Broer, Linda, Janssens, Cecile, Catsman-Berrevoets, Coriene E, van Duijn, Cornelia M, Banwell, Brenda, Bar-Or, Amit, Hintzen, Rogier Q
Published in Neurology (03.12.2013)
Published in Neurology (03.12.2013)
Get more information
Journal Article
EBNA-1 titer gradient in families with multiple sclerosis indicates a genetic contribution
Mescheriakova, Julia Y, van Nierop, Gijsbert P, van der Eijk, Annemiek A, Kreft, Karim L, Hintzen, Rogier Q
Published in Neurology : neuroimmunology & neuroinflammation (05.11.2020)
Published in Neurology : neuroimmunology & neuroinflammation (05.11.2020)
Get full text
Journal Article
Fatigue after a first attack of suspected multiple sclerosis
van der Vuurst de Vries, Roos M, van den Dorpel, Jan JA, Mescheriakova, Julia Y, Runia, Tessel F, Jafari, Naghmeh, Siepman, Theodora AM, Rizopoulos, Dimitris, Steyerberg, Ewout W, Hintzen, Rogier Q
Published in Multiple sclerosis (01.06.2018)
Published in Multiple sclerosis (01.06.2018)
Get full text
Journal Article
Burden of genetic risk variants in multiple sclerosis families in the Netherlands
Mescheriakova, Julia Y, Broer, Linda, Wahedi, Simin, Uitterlinden, André G, van Duijn, Cornelia M, Hintzen, Rogier Q
Published in Multiple sclerosis journal - experimental, translational and clinical (01.01.2016)
Published in Multiple sclerosis journal - experimental, translational and clinical (01.01.2016)
Get full text
Journal Article
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis
LILL, Christina M, SCHJEIDE, Brit-Maren M, BROER, Linda, SCHILLING, Marcel, AKKAD, Denis A, AKTAS, Orhan, ALLOZA, Iraide, ANTIGÜEDAD, Alfredo, ARROYO, Rafa, BLASCHKE, Paul, BUTTMANN, Mathias, CHAN, Andrew, GRAETZ, Christiane, COMPSTON, Alastair, COURNU-REBEIX, Isabelle, DÖRNER, Thomas, EPPLEN, Joerg T, FERNANDEZ, Oscar, CERDES, Lisa-Ann, GUILLOT-NOËL, Léna, HARTUNG, Hans-Peter, HOFFJAN, Sabine, IZQUIERDO, Guillermo, BAN, Maria, KEMPPINEN, Anu, KRONER, Antje, KUBISCH, Christian, KÜMPFEL, Tania, LI, Shu-Chen, LINDENBERGER, Ulman, LOHSE, Peter, LUBETZKI, Catherine, LUESSI, Felix, MALHOTRA, Sunny, ALCINA, Antonio, MESCHERIAKOVA, Julia, MONTALBAN, Xavier, PAPEIX, Caroline, PAREDES, Lidia F, RIECKMANN, Peter, STEINHAGEN-THIESSEN, Elisabeth, WINKELMANN, Alexander, ZETTL, Uwe K, HINTZEN, Rogier, VANDENBROECK, Koen, ORTIZ, Miguel A, STEWART, Graeme, FONTAINE, Bertrand, COMABELLA, Manuel, URCELAY, Elena, MATESANZ, Fuencisla, SAWCER, Stephen, BERTRAM, Lars, ZIPP, Frauke, PEREZ, Jennifer, DAMOTTE, Vincent, BOOTH, David, DE LAPUENTE, Aitzkoa Lopez
Published in Brain (London, England : 1878) (01.06.2013)
Published in Brain (London, England : 1878) (01.06.2013)
Get full text
Journal Article
Web Resource
Genome-wide significant association with seven novel multiple sclerosis risk loci
Lill, Christina M, Luessi, Felix, Alcina, Antonio, Sokolova, Ekaterina A, Ugidos, Nerea, de la Hera, Belén, Guillot-Noël, Léna, Malhotra, Sunny, Reinthaler, Eva, Schjeide, Brit-Maren M, Mescheriakova, Julia Y, Mashychev, Andriy, Wohlers, Inken, Akkad, Denis A, Aktas, Orhan, Alloza, Iraide, Antigüedad, Alfredo, Arroyo, Rafa, Astobiza, Ianire, Blaschke, Paul, Boyko, Alexei N, Buttmann, Mathias, Chan, Andrew, Dörner, Thomas, Epplen, Joerg T, Favorova, Olga O, Fedetz, Maria, Fernández, Oscar, García-Martínez, Angel, Gerdes, Lisa-Ann, Graetz, Christiane, Hartung, Hans-Peter, Hoffjan, Sabine, Izquierdo, Guillermo, Korobko, Denis S, Kroner, Antje, Kubisch, Christian, Kümpfel, Tania, Leyva, Laura, Lohse, Peter, Malkova, Nadezhda A, Montalban, Xavier, Popova, Ekaterina V, Rieckmann, Peter, Rozhdestvenskii, Alexei S, Schmied, Christiane, Smagina, Inna V, Tsareva, Ekaterina Y, Winkelmann, Alexander, Zettl, Uwe K, Binder, Harald, Cournu-Rebeix, Isabelle, Hintzen, Rogier, Zimprich, Alexander, Comabella, Manuel, Fontaine, Bertrand, Urcelay, Elena, Vandenbroeck, Koen, Filipenko, Maxim, Matesanz, Fuencisla, Zipp, Frauke, Bertram, Lars
Published in Journal of medical genetics (01.12.2015)
Published in Journal of medical genetics (01.12.2015)
Get full text
Journal Article
Polymorphisms in CACNA1E and Camk2d are associated with seizure susceptibility of Sprague–Dawley rats
Rijkers, Kim, Mescheriakova, Julia, Majoie, Marian, Lemmens, Evi, van Wijk, Xander, Philippens, Marjan, Van Kranen-Mastenbroek, Vivianne, Schijns, Olaf, Vles, Johannes, Hoogland, Govert
Published in Epilepsy research (01.09.2010)
Published in Epilepsy research (01.09.2010)
Get full text
Journal Article
Application of the 2017 Revised McDonald Criteria for Multiple Sclerosis to Patients With a Typical Clinically Isolated Syndrome
de Vries, Roos M van der Vuurst, Mescheriakova, Julia Y, Wong, Yu Yi M, Runia, Tessel F, Jafari, Naghmeh, Samijn, Johnny P, de Beukelaar, Janet W K, Wokke, Beatrijs H A, Siepman, Theodora A M, Hintzen, Rogier Q
Published in Archives of neurology (Chicago) (01.11.2018)
Get full text
Published in Archives of neurology (Chicago) (01.11.2018)
Journal Article