Analysis of blood-based gene expression in idiopathic Parkinson disease von Shamir, Ron, Amar, David

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Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor von Liao, Calwing, Sarayloo, Faezeh, Rochefort, Daniel, Houle, Gabrielle, Akçimen, Fulya, He, Qin, Laporte, Alexandre D., Spiegelman, Dan, Poewe, Werner, Berg, Daniela, Müller, Stefanie, Hopfner, Franziska, Deuschl, Günther, Kuhlenbäeumer, Gregor, Rajput, Alex, Dion, Patrick A., Rouleau, Guy A.

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Quantitative Vascular Pathology and Phenotyping Familial and Sporadic Cerebral Small Vessel Diseases von Craggs, Lucinda J. L., Hagel, Christian, Kuhlenbaeumer, Gregor, Borjesson-Hanson, Anne, Andersen, Oluf, Viitanen, Matti, Kalimo, Hannu, McLean, Catriona A., Slade, Janet Y., Hall, Roslyn A., Oakley, Arthur E., Yamamoto, Yumi, Deramecourt, Vincent, Kalaria, Rajesh N.

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Gut microbiota in Parkinson disease in a northern German cohort von Hopfner, Franziska, Künstner, Axel, Müller, Stefanie H, Künzel, Sven, Zeuner, Kirsten E, Margraf, Nils G, Deuschl, Günther, Baines, John F, Kuhlenbäumer, Gregor

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Genetics of essential tremor: Meta-analysis and review von Kuhlenbäumer, Gregor, Hopfner, Franziska, Deuschl, Günther

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β-adrenoreceptors and the risk of Parkinson's disease von Hopfner, Franziska, Höglinger, Günter U, Kuhlenbäumer, Gregor, Pottegård, Anton, Wod, Mette, Christensen, Kaare, Tanner, Caroline M, Deuschl, Günther

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Decreased Cerebrospinal Fluid Amyloid Beta 38, 40, 42, and 43 Levels in Sporadic and Hereditary Cerebral Amyloid Angiopathy von Kuhlenbäumer, Gregor, Jensen‐Kondering, Ulf, Margraf, Nils G.

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Early- and late-onset essential tremor patients represent clinically distinct subgroups von Hopfner, Franziska, Ahlf, Anjuli, Lorenz, Delia, Klebe, Stephan, Zeuner, Kirsten E., Kuhlenbäumer, Gregor, Deuschl, Günther

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Novel genomic techniques open new avenues in the analysis of monogenic disorders von Kuhlenbäumer, Gregor, Hullmann, Julia, Appenzeller, Silke

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Family and literature analysis demonstrates phenotypic effect of two variants in the calpain-3 gene von Tomforde, Maike, Steinbach, Meike, Haack, Tobias B., Kuhlenbäumer, Gregor

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De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies von Appenzeller, Silke, Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, De Jonghe, Peter, Depienne, Christel, Dimova, Petia, Djémié, Tania, Gormley, Padhraig, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Jähn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Kuhlenbäumer, Gregor, Lemke, Johannes R., Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Møller, Rikke S., Muhle, Hiltrud, Palotie, Aarno, Pendziwiat, Manuela, Roelens, Filip, Rosenow, Felix, Selmer, Kaja, Serratosa, Jose M., Sisodiya, Sanjay, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weckhuysen, Sarah, Abou-Khalil, Bassel, Alldredge, Brian K., Andermann, Eva, Andermann, Frederick, Amron, Dina, Bautista, Jocelyn F., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alex, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Fiol, Miguel, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R., Hayward, Jean, Helmers, Sandra L., Joshi, Sucheta, Kanner, Andres, Knowlton, Robert C., Kossoff, Eric H., Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Novotny, Edward J., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack, Park, Kristen, Scheffer, Ingrid E., Shellhaas, Renée A., Sherr, Elliott, Singh, Rani, Smith, Michael C., Sullivan, Joe, Venkat, Anu, Vining, Eileen P.G., Von Allmen, Gretchen K., Weisenberg, Judith L., Winawer, Melodie R., Cossette, Patrick, Delanty, Norman, Eichler, Evan E., Goldstein, David B., Han, Yujun, Heinzen, Erin L., Marson, Anthony G., Nieh, Sahar Esmaeeli, O’Brien, Terence J., Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K.

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Neurofilament light (NfL) concentrations in patients with epilepsy with recurrent isolated seizures: Insights from a clinical cohort study von Dargvainiene, Justina, Sahaf, Safa, Franzenburg, Jeanette, Matthies, Inga, Leypoldt, Frank, Wandinger, Klaus-Peter, Baysal, Leyla, Markewitz, Robert, Kuhlenbäumer, Gregor, Margraf, Nils G.

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Electroencephalography based delirium screening in acute supratentorial stroke von Hermann, Gesine, Baumgarte, Friederike, Welzel, Julius, Nydahl, Peter, Kuhlenbäumer, Gregor, Margraf, Nils Gerd

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Clinical, serological and genetic predictors of response to immunotherapy in anti-IgLON5 disease von Grüter, Thomas, Möllers, Franziska E, Tietz, Anja, Dargvainiene, Justina, Melzer, Nico, Heidbreder, Anna, Strippel, Christine, Kraft, Andrea, Höftberger, Romana, Schöberl, Florian, Thaler, Franziska S, Wickel, Jonathan, Chung, Ha-Yeun, Seifert, Frank, Tschernatsch, Marlene, Nagel, Michael, Lewerenz, Jan, Jarius, Sven, Wildemann, Brigitte C, de Azevedo, Lucie, Heidenreich, Fedor, Heusgen, Raphaela, Hofstadt-van Oy, Ulrich, Linsa, Andreas, Maaß, Jannis Justus, Menge, Til, Ringelstein, Marius, Pedrosa, David J, Schill, Josef, Seifert-Held, Thomas, Seitz, Caspar, Tonner, Silke, Urbanek, Christian, Zittel, Simone, Markewitz, Robert, Korporal-Kuhnke, Mirjam, Schmitter, Thomas, Finke, Carsten, Brüggemann, Norbert, Bien, Corinna I, Kleiter, Ingo, Gold, Ralf, Wandinger, Klaus-Peter, Kuhlenbäumer, Gregor, Leypoldt, Frank, Ayzenberg, Ilya

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Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus von Margraf, Nils G., Dargvainiene, Justina, Theel, Emily, Leypoldt, Frank, Lieb, Wolfgang, Franke, Andre, Berger, Klaus, Kuhle, Jens, Kuhlenbaeumer, Gregor

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Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease von Hopfner, Franziska, Mueller, Stefanie H., Szymczak, Silke, Junge, Olaf, Tittmann, Lukas, May, Sandra, Lohmann, Katja, Grallert, Harald, Lieb, Wolfgang, Strauch, Konstantin, Müller‐Nurasyid, Martina, Berger, Klaus, Schormair, Barbara, Winkelmann, Juliane, Mollenhauer, Brit, Trenkwalder, Claudia, Maetzler, Walter, Berg, Daniela, Kasten, Meike, Klein, Christine, Höglinger, Günter U., Gasser, Thomas, Deuschl, Günther, Franke, André, Krawczak, Michael, Dempfle, Astrid, Kuhlenbäumer, Gregor

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Genetic predisposition in anti‐LGI1 and anti‐NMDA receptor encephalitis von Mueller, Stefanie H., Färber, Anna, Golombeck, Kristin S., Kümpfel, Tania, Kaufmann, Max, Ringelstein, Marius, Kellinghaus, Christoph, Ehrlich, Sven, Then Bergh, Florian, Faiss, Jürgen H., Franke, Andre, Lyss, Birgit, Wallenfelsova, Eva, Othman, Jalal, Bogarin, Yuri, Schwabe, Julia, Handreka, Robert, Rostasy, Kevin, Körber, Rüdiger, Heide, Wolfgang, Geis, Tobias, Dogan, Muejgan, Bien, Christian, Kramme, Corinna, Pulkowski, Ulrich, Hoepner, Robert, Schindler, Kaspar, Lippert, Julian, Ewering, Carina, Reimann, Gemot, Schimrigk, Sebastian, Urbanek, Christian, Schön, Frauke, Finke, Alexander, Henningsen, Henning, Küpper, Philipp, Kellinghaus, Christoph, Hofstadt, Ulrich, Trendelenburg, George, Heider, Steffen, Thaler, Franziska, Muth, Carolin, Borggräfe, Ingo, Blaschek, Astrid, Kümpfel, Tania, Bieniek, Rolf, Philipsen, Alexandra, Winter, Benjamin, Gass, Achim, Hagenah, Ulrich, Hausler, Martin Georg, Tauber, Simone, Elger, Christian, Spruth, Eike, Paul, Friedemann, Finke, Carsten, Prüss, Harald, Wöpking, Sigrid, Schneider, Auke, Seitz, Rüdiger, Ringelstein, Marius, Aktas, Orhan, Huttner, Hagen, Stich, Oliver, Baumgartner, Annette, Neubauer, Bemd, Döppner, Thorsten, Süße, M, Heesen, Christoph, Friese, Manuel, Sühs, Kurt‐Wolfram, Trebst, Corinna, Wildemann, Brigitte, Bösel, Julian, Roepke, Luise, Brämer, Dirk, Strubl, Julia, Günther, Albrecht, Bergh, Florian Then, Schilling, Ruth, Bittner, Daniel, Spreer, Annette, Methner, Axel, Pledl, Hans‐Wemer, Anlonso, Angelika, Szabo, Kristina, Philipp, Konstanze, Möning, Constanze, Weissert, Robert, Retzlaff, Nele, Fousse, Mathias, Ragoschke‐Schumm, Andreas, Stumer, Klarissa, Berg, Daniela, Schmütz, Isa, Bartsch, Thorsten, Falk, Kim Christin, Hummel, Katja, Tumani, Hayrettin, Lewerenz, Jan

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Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies von Traylor, Matthew, MSc, Farrall, Martin, FRCPath, Holliday, Elizabeth G, PhD, Sudlow, Cathie, FRCP, Hopewell, Jemma C, PhD, Cheng, Yu-Ching, PhD, Fornage, Myriam, PhD, Ikram, M Arfan, MD, Malik, Rainer, PhD, Bevan, Steve, PhD, Thorsteinsdottir, Unnur, PhD, Nalls, Mike A, PhD, Longstreth, WT, MD, Wiggins, Kerri L, MS, Yadav, Sunaina, MSc, Parati, Eugenio A, MD, DeStefano, Anita L, PhD, Worrall, Bradford B, MD, Kittner, Steven J, MD, Khan, Muhammad Saleem, MSc, Reiner, Alex P, MD, Helgadottir, Anna, MD, Achterberg, Sefanja, PhD, Fernandez-Cadenas, Israel, PhD, Abboud, Sherine, MD, Schmidt, Reinhold, MD, Walters, Matthew, MD, Chen, Wei-Min, PhD, Ringelstein, E Bernd, MD, O'Donnell, Martin, MD, Ho, Weang Kee, PhD, Pera, Joanna, MD, Lemmens, Robin, MD, Norrving, Bo, MD, Higgins, Peter, MRCP, Benn, Marianne, MD, Sale, Michele, PhD, Kuhlenbäumer, Gregor, MD, Doney, Alexander S F, PhD, Vicente, Astrid M, PhD, Delavaran, Hossein, MD, Algra, Ale, MD, Davies, Gail, PhD, Oliveira, Sofia A, PhD, Palmer, Colin N A, PhD, Deary, Ian, PhD, Schmidt, Helena, MD, Pandolfo, Massimo, MD, Montaner, Joan, MD, Carty, Cara, PhD, de Bakker, Paul I W, PhD, Kostulas, Konstantinos, MD, Ferro, Jose M, MD, van Zuydam, Natalie R, MSc, Valdimarsson, Einar, MD, Nordestgaard, Børge G, MD, Lindgren, Arne, MD, Thijs, Vincent, MD, Slowik, Agnieszka, MD, Saleheen, Danish, MD, Paré, Guillaume, MD, Berger, Klaus, MD, Thorleifsson, Gudmar, PhD, Hofman, Albert, MD, Mosley, Thomas H, PhD, Mitchell, Braxton D, PhD, Furie, Karen, MD, Clarke, Robert, FRCP, Levi, Christopher, MD, Seshadri, Sudha, MD, Gschwendtner, Andreas, MD, Boncoraglio, Giorgio B, MD, Sharma, Pankaj, PhD, Bis, Joshua C, PhD, Gretarsdottir, Solveig, PhD, Psaty, Bruce M, Rothwell, Peter M, FMedSci, Rosand, Jonathan, MD, Meschia, James F, MD, Stefansson, Kari, MD, Dichgans, Martin, MD, Markus, Hugh S, Dr

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Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules von Bai, Xiaobo, Bowen, Jonathan R, Knox, Tara K, Zhou, Kaifeng, Pendziwiat, Manuela, Kuhlenbäumer, Gregor, Sindelar, Charles V, Spiliotis, Elias T

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Clinical and radiological differences between patients with probable cerebral amyloid angiopathy and mixed cerebral microbleeds von Jensen-Kondering, Ulf R., Weiler, Caroline, Langguth, Patrick, Larsen, Naomi, Flüh, Charlotte, Kuhlenbäumer, Gregor, Jansen, Olav, Margraf, Nils G.

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