Varicella zoster-associated retinal and central nervous system vasculitis in a patient with multiple sclerosis treated with natalizumab

od Kobeleva, Xenia, Wegner, Florian, Brunotte, Inez, Dadak, Mete, Dengler, Reinhard, Stangel, Martin
Wydane 2014

Working Memory Network Changes in ALS: An fMRI Study

od Vellage, Anne-Katrin, Veit, Maria, Kobeleva, Xenia, Petri, Susanne, Vielhaber, Stefan, Müller, Notger G.
Wydane w Front Neurosci (2016)

Clinically Applicable Quantitative Magnetic Resonance Morphologic Measurements of Grey Matter Changes in the Human Brain

od Fu, Tong, Kobeleva, Xenia, Bronzlik, Paul, Nösel, Patrick, Dadak, Mete, Lanfermann, Heinrich, Petri, Susanne, Ding, Xiao-Qi
Wydane w Brain Sci (2021)

Divergent functional connectivity during attentional processing in Lewy body dementia and Alzheimer's disease

od Kobeleva, Xenia, Firbank, Michael, Peraza, Luis, Gallagher, Peter, Thomas, Alan, Burn, David J., O'Brien, John, Taylor, John-Paul
Wydane w Cortex (2017)

E-learning preferences of European junior neurologists—an EAYNT survey

od Sztriha, Laszlo K., Varga, Edina T., Róna-Vörös, Krisztina, Holler, Natalja, Ilea, Raluca, Kobeleva, Xenia, Falup-Pecurariu, Cristian, Struhal, Walter, Sellner, Johann
Wydane 2012

Neural correlates of attention‐executive dysfunction in lewy body dementia and Alzheimer's disease

od Firbank, Michael, Kobeleva, Xenia, Cherry, George, Killen, Alison, Gallagher, Peter, Burn, David J., Thomas, Alan J., O'Brien, John T., Taylor, John‐Paul
Wydane w Hum Brain Mapp (2015)

Electroencephalographic derived network differences in Lewy body dementia compared to Alzheimer’s disease patients

od Peraza, Luis R., Cromarty, Ruth, Kobeleva, Xenia, Firbank, Michael J., Killen, Alison, Graziadio, Sara, Thomas, Alan J., O’Brien, John T., Taylor, John-Paul
Wydane w Sci Rep (2018)

Neuropsychiatric symptoms in at-risk groups for AD dementia and their association with worry and AD biomarkers—results from the DELCODE study

od Sannemann, Lena, Schild, Ann-Katrin, Altenstein, Slawek, Bartels, Claudia, Brosseron, Frederic, Buerger, Katharina, Cosma, Nicoleta Carmen, Fliessbach, Klaus, Freiesleben, Silka Dawn, Glanz, Wenzel, Heneka, Michael T., Janowitz, Daniel, Kilimann, Ingo, Kobeleva, Xenia, Laske, Christoph, Metzger, Coraline D., Munk, Matthias H. J., Perneczky, Robert, Peters, Oliver, Polcher, Alexandra, Priller, Josef, Rauchmann, Boris, Rösch, Christina, Rudolph, Janna, Schneider, Anja, Spottke, Annika, Spruth, Eike Jakob, Teipel, Stefan, Vukovich, Ruth, Wagner, Michael, Wiltfang, Jens, Wolfsgruber, Steffen, Duezel, Emrah, Jessen, Frank
Wydane w Alzheimers Res Ther (2020)

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

od Farazi Fard, Mohammad Ali, Rebelo, Adriana P., Buglo, Elena, Nemati, Hamid, Dastsooz, Hassan, Gehweiler, Ina, Reich, Selina, Reichbauer, Jennifer, Quintáns, Beatriz, Ordóñez-Ugalde, Andrés, Cortese, Andrea, Courel, Steve, Abreu, Lisa, Powell, Eric, Danzi, Matt, Martuscelli, Nicole B., Bis-Brewer, Dana M., Tao, Feifei, Zarei, Fariba, Habibzadeh, Parham, Yavarian, Majid, Modarresi, Farzaneh, Silawi, Mohammad, Tabatabaei, Zahra, Yousefi, Masoume, Farpour, Hamid Reza, Kessler, Christoph, Mangold, Elisabeth, Kobeleva, Xenia, Mueller, Amelie J., Haack, Tobias B., Tarnopolsky, Mark, Gan-Or, Ziv, Rouleau, Guy A., Synofzik, Matthis, Sobrido, María-Jesús, Jordanova, Albena, Schüle, Rebecca, Zuchner, Stephan, Faghihi, Mohammad Ali
Wydane w Am J Hum Genet (2019)

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

od Farazi Fard, Mohammad Ali, Rebelo, Adriana P., Buglo, Elena, Nemati, Hamid, Dastsooz, Hassan, Gehweiler, Ina, Reich, Selina, Reichbauer, Jennifer, Quintáns, Beatriz, Ordóñez-Ugalde, Andrés, Cortese, Andrea, Courel, Steve, Abreu, Lisa, Powell, Eric, Danzi, Matt C., Martuscelli, Nicole B., Bis-Brewer, Dana M., Tao, Feifei, Zarei, Fariba, Habibzadeh, Parham, Yavarian, Majid, Modarresi, Farzaneh, Silawi, Mohammad, Tabatabaei, Zahra, Yousefi, Masoume, Farpour, Hamid Reza, Kessler, Christoph, Mangold, Elisabeth, Kobeleva, Xenia, Tournev, Ivailo, Chamova, Teodora, Mueller, Amelie J., Haack, Tobias B., Tarnopolsky, Mark, Gan-Or, Ziv, Rouleau, Guy A., Synofzik, Matthis, Sobrido, María-Jesús, Jordanova, Albena, Schüle, Rebecca, Zuchner, Stephan, Faghihi, Mohammad Ali
Wydane w Am J Hum Genet (2019)

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

od Husain, Ralf A., Grimmel, Mona, Wagner, Matias, Hennings, J. Christopher, Marx, Christian, Feichtinger, René G., Saadi, Abdelkrim, Rostásy, Kevin, Radelfahr, Florentine, Bevot, Andrea, Döbler-Neumann, Marion, Hartmann, Hans, Colleaux, Laurence, Cordts, Isabell, Kobeleva, Xenia, Darvish, Hossein, Bakhtiari, Somayeh, Kruer, Michael C., Besse, Arnaud, Ng, Andy Cheuk-Him, Chiang, Diana, Bolduc, Francois, Tafakhori, Abbas, Mane, Shrikant, Ghasemi Firouzabadi, Saghar, Huebner, Antje K., Buchert, Rebecca, Beck-Woedl, Stefanie, Müller, Amelie J., Laugwitz, Lucia, Nägele, Thomas, Wang, Zhao-Qi, Strom, Tim M., Sturm, Marc, Meitinger, Thomas, Klockgether, Thomas, Riess, Olaf, Klopstock, Thomas, Brandl, Ulrich, Hübner, Christian A., Deschauer, Marcus, Mayr, Johannes A., Bonnen, Penelope E., Krägeloh-Mann, Ingeborg, Wortmann, Saskia B., Haack, Tobias B.
Wydane w Am J Hum Genet (2020)