Items where Author or Editor is "Synofzik, Matthis" - Kölner UniversitätsPublikationsServer

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Number of items: 13.

Journal Article

Brosseron, Frederic ORCID: 0000-0003-3137-7516, Maass, Anne, Kleineidam, Luca, Ravichandran, Kishore Aravind ORCID: 0000-0002-2429-5988, Gonzalez, Pablo Garcia, McManus, Roisin M., Ising, Christina ORCID: 0000-0002-7267-3488, Santarelli, Francesco, Kolbe, Carl-Christian, Haesler, Lisa M., Wolfsgruber, Steffen, Marquie, Marta, Boada, Merce ORCID: 0000-0003-2617-3009, Orellana, Adelina ORCID: 0000-0002-0204-1944, de Rojas, Itziar, Roeske, Sandra, Peters, Oliver ORCID: 0000-0003-0568-2998, Cosma, Nicoleta-Carmen, Cetindag, Arda, Wang, Xiao, Priller, Josef, Spruth, Eike J., Altenstein, Slawek ORCID: 0000-0003-2753-5999, Schneider, Anja ORCID: 0000-0001-9540-8700, Fliessbach, Klaus, Wiltfang, Jens, Schott, Bjorn H., Buerger, Katharina, Janowitz, Daniel, Dichgans, Martin ORCID: 0000-0002-0654-387X, Perneczky, Robert, Rauchmann, Boris-Stephan ORCID: 0000-0003-4547-6240, Teipel, Stefan, Kilimann, Ingo, Goerss, Doreen, Laske, Christoph, Munk, Matthias H., Duzel, Emrah, Yakupov, Renat, Dobisch, Laura, Metzger, Coraline D., Glanz, Wenzel, Ewers, Michael, Dechent, Peter, Haynes, John Dylan, Scheffler, Klaus, Roy, Nina, Rostamzadeh, Ayda ORCID: 0000-0001-5189-134X, Teunissen, Charlotte E., Marchant, Natalie L., Spottke, Annika, Jucker, Mathias, Latz, Eicke ORCID: 0000-0003-1488-5666, Wagner, Michael, Mengel, David, Synofzik, Matthis, Jessen, Frank, Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Ruiz, Agustin and Heneka, Michael T. (2022). Soluble TAM receptors sAXL and sTyro3 predict structural and functional protection in Alzheimer's disease. Neuron, 110 (6). S. 1009 - 1028. CAMBRIDGE: CELL PRESS. ISSN 1097-4199

Brosseron, Frederic ORCID: 0000-0003-3137-7516, Maass, Anne ORCID: 0000-0002-7889-795X, Kleineidam, Luca, Ravichandran, Kishore Aravind ORCID: 0000-0002-2429-5988, González, Pablo García, McManus, Róisín M. ORCID: 0000-0002-6896-0302, Ising, Christina ORCID: 0000-0002-7267-3488, Santarelli, Francesco, Kolbe, Carl-Christian, Häsler, Lisa M., Wolfsgruber, Steffen, Marquie, Marta ORCID: 0000-0002-0660-0950, Boada, Merce ORCID: 0000-0003-2617-3009, Orellana, Adelina ORCID: 0000-0002-0204-1944, de Rojas, Itziar ORCID: 0000-0002-2148-381X, Röske, Sandra, Peters, Oliver ORCID: 0000-0003-0568-2998, Cosma, Nicoleta-Carmen ORCID: 0000-0002-2656-8046, Cetindag, Arda, Wang, Xiao, Priller, Josef ORCID: 0000-0001-7596-0979, Spruth, Eike J., Altenstein, Slawek ORCID: 0000-0003-2753-5999, Schneider, Anja ORCID: 0000-0001-9540-8700, Fliessbach, Klaus, Wiltfang, Jens ORCID: 0000-0003-1492-5330, Schott, Björn H., Bürger, Katharina, Janowitz, Daniel, Dichgans, Martin ORCID: 0000-0002-0654-387X, Perneczky, Robert ORCID: 0000-0003-1981-7435, Rauchmann, Boris-Stephan ORCID: 0000-0003-4547-6240, Teipel, Stefan J. ORCID: 0000-0002-3586-3194, Kilimann, Ingo ORCID: 0000-0002-3269-4452, Görß, Doreen ORCID: 0000-0002-5336-8349, Laske, Christoph, Munk, Matthias H. ORCID: 0000-0002-5339-4045, Duzel, Emrah ORCID: 0000-0002-0139-5388, Yakupov, Renat, Dobisch, Laura, Metzger, Coraline D., Glanz, Wenzel ORCID: 0000-0002-5865-4176, Ewers, Michael ORCID: 0000-0001-5231-1714, Dechent, Peter, Haynes, John Dylan ORCID: 0000-0003-1786-6954, Scheffler, Klaus ORCID: 0000-0001-6316-8773, Roy, Nina, Rostamzadeh, Ayda ORCID: 0000-0001-5189-134X, Teunissen, Charlotte E. ORCID: 0000-0002-4061-0837, Marchant, Natalie L. ORCID: 0000-0003-0669-6910, Spottke, Annika, Jucker, Mathias ORCID: 0000-0001-9045-1072, Latz, Eicke ORCID: 0000-0003-1488-5666, Wagner, Michael ORCID: 0000-0003-2589-6440, Mengel, David, Synofzik, Matthis ORCID: 0000-0002-2280-7273, Jessen, Frank ORCID: 0000-0003-1067-2102, Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Ruiz, Agustin ORCID: 0000-0003-2633-2495 and Heneka, Michael T. ORCID: 0000-0003-4996-1630 (2022). Soluble TAM receptors sAXL and sTyro3 predict structural and functional protection in Alzheimer’s disease. Neuron, 110 (6). 1009-1022.e4. Cell Press. ISSN 0896-6273

Huber, Meret K., Raichle, Claudia, Lingor, Paul, Synofzik, Matthis ORCID: 0000-0002-2280-7273, Borgmann, Stefan, Erber, Johanna ORCID: 0000-0001-6614-6051, Tometten, Lukas ORCID: 0000-0002-5968-8335, Rimili, Wolfgang, Dolff, Sebastian, Wille, Kai, Knauss, Samuel, Piepel, Christiane, Lanznaster, Julia, Rieg, Siegbert, Prasser, Fabian ORCID: 0000-0003-3172-3095, Pilgram, Lisa, Spottke, Annika, Klockgether, Thomas, Klein, Christine, Hopfner, Franziska ORCID: 0000-0001-6524-0281 and Hoeglinger, Guenter U. (2021). Outcomes of SARS-CoV-2 Infections in Patients With Neurodegenerative Diseases in the LEOSS Cohort. Mov. Disord., 36 (4). S. 791 - 794. HOBOKEN: WILEY. ISSN 1531-8257

Koutsouleris, Nikolaos, Pantelis, Christos, Velakoulis, Dennis, McGuire, Philip, Dwyer, Dominic B., Urquijo-Castro, Maria-Fernanda, Paul, Riya, Popovic, David, Oeztuerk, Oemer, Kambeitz, Joseph, Salokangas, Raimo K. R., Hietala, Jarmo ORCID: 0000-0002-3179-6780, Bertolino, Alessandro, Brambilla, Paolo, Upthegrove, Rachel ORCID: 0000-0001-8204-5103, Wood, Stephen J., Lencer, Rebekka, Borgwardt, Stefan, Maj, Carlo, Nothen, Markus, Degenhardt, Franziska, Polyakova, Maryna, Mueller, Karsten, Villringer, Arno, Danek, Adrian ORCID: 0000-0001-8857-5383, Fassbender, Klaus ORCID: 0000-0003-3596-868X, Fliessbach, Klaus, Jahn, Holger ORCID: 0000-0003-3607-7651, Kornhuber, Johannes, Landwehrmeyer, Bernhard, Anderl-Straub, Sarah, Prudlo, Johannes, Synofzik, Matthis, Wiltfang, Jens, Riedl, Lina, Diehl-Schmid, Janine, Otto, Markus ORCID: 0000-0003-4273-4267, Meisenzahl, Eva, Falkai, Peter and Schroeter, Matthias L. (2022). Exploring Links Between Psychosis and Frontotemporal Dementia Using Multimodal Machine Learning Dementia Praecox Revisited. JAMA Psychiatry, 79 (9). S. 907 - 920. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6238

Minnerop, Martina, Kurzwelly, Delia, Rattay, Tim W. ORCID: 0000-0002-5456-7761, Timmann, Dagmar, Hengel, Holger, Synofzik, Matthis, Stendel, Claudia, Horvath, Rita ORCID: 0000-0002-9841-170X, Schuele, Rebecca and Ramirez, Alfredo ORCID: 0000-0003-4991-763X (2018). Reply: POLR3A variants in hereditary spastic paraplegia and ataxia. Brain, 141. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

Minnerop, Martina, Kurzwelly, Delia, Wagner, Holger, Soehn, Anne S., Reichbauer, Jennifer, Tao, Feifei, Rattay, Tim W. ORCID: 0000-0002-5456-7761, Peitz, Michael, Rehbach, Kristina, Giorgetti, Alejandro, Pyle, Angela, Thiele, Holger, Altmueller, Janine, Timmann, Dagmar, Karaca, Ilker, Lennarz, Martina, Baets, Jonathan, Hengel, Holger, Synofzik, Matthis, Atasu, Burcu, Feely, Shawna, Kennerson, Marina, Stendel, Claudia, Lindig, Tobias, Gonzalez, Michael A., Stirnberg, Ruediger, Sturm, Marc ORCID: 0000-0002-6552-8362, Roeske, Sandra, Jung, Johanna, Bauer, Peter, Lohmann, Ebba, Herms, Stefan ORCID: 0000-0002-2786-8200, Heilmann-Heimbach, Stefanie ORCID: 0000-0003-1057-465X, Nicholson, Garth, Mahanjah, Muhammad, Sharkia, Rajech, Carloni, Paolo, Bruestle, Oliver, Klopstock, Thomas, Mathews, Katherine D., Shy, Michael E., de Jonghe, Peter, Chinnery, Patrick F., Horvath, Rita ORCID: 0000-0002-9841-170X, Kohlhase, Juergen, Schmitt, Ina, Wolf, Michael, Greschus, Susanne, Amunts, Katrin, Maier, Wolfgang, Schoels, Ludger, Nuernberg, Peter, Zuchner, Stephan, Klockgether, Thomas, Ramirez, Alfredo ORCID: 0000-0003-4991-763X and Schuele, Rebecca (2017). Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. Brain, 140. S. 1561 - 1579. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

Schlaepfer, Thomas E., Meyer-Lindenberg, Andreas, Synofzik, Matthis, Visser-Vandewalle, Veerle, Voges, Juergen and Coenen, Volker A. (2021). Invasive Brain Stimulation in the Treatment of Psychiatric Illness Proposed Indications and Approaches. Dtsch. Arztebl. Int., 118 (3). S. 31 - 41. COLOGNE: DEUTSCHER AERZTE-VERLAG GMBH. ISSN 1866-0452

Synofzik, Matthis ORCID: 0000-0002-2280-7273, Martinez-Carrera, Lilian A., Lindig, Tobias, Schoels, Ludger and Wirth, Brunhilde ORCID: 0000-0003-4051-5191 (2014). Dominant spinal muscular atrophy due to BICD2: a novel mutation refines the phenotype. J. Neurol. Neurosurg. Psychiatry, 85 (5). S. 590 - 593. LONDON: BMJ PUBLISHING GROUP. ISSN 1468-330X

Syrbe, Steffen, Hedrich, Ulrike B. S., Riesch, Erik, Djemie, Tania, Mueller, Stephan, Moller, Rikke S., Maher, Bridget ORCID: 0000-0002-9735-0845, Hernandez-Hernandez, Laura, Synofzik, Matthis ORCID: 0000-0002-2280-7273, Caglayan, Hande S., Arslan, Mutluay, Serratosa, Jose M., Nothnagel, Michael ORCID: 0000-0001-8305-7114, May, Patrick ORCID: 0000-0001-8698-3770, Krause, Roland ORCID: 0000-0001-9938-7126, Loeffler, Heidrun, Detert, Katja, Dorn, Thomas, Vogt, Heinrich, Kraemer, Guenter, Schoels, Ludger, Mullis, Primus E., Linnankivi, Tarja, Lehesjoki, Anna-Elina, Sterbova, Katalin, Craiu, Dana C., Hoffman-Zacharska, Dorota ORCID: 0000-0001-7367-512X, Korff, Christian M., Weber, Yvonne G., Steinlin, Maja, Gallati, Sabina, Bertsche, Astrid ORCID: 0000-0003-2832-0156, Bernhard, Matthias K., Merkenschlager, Andreas, Kiess, Wieland, Gonzalez, Michael, Zuechner, Stephan, Palotie, Aarno, Suls, Arvid ORCID: 0000-0003-0328-198X, De Jonghe, Peter, Helbig, Ingo ORCID: 0000-0001-8486-0558, Biskup, Saskia, Wolff, Markus ORCID: 0000-0001-5640-0888, Maljevic, Snezana ORCID: 0000-0003-1876-5872, Schule, Rebecca ORCID: 0000-0002-7781-2766, Sisodiya, Sanjay M., Weckhuysen, Sarah ORCID: 0000-0003-2878-1147, Lerche, Holger and Lemke, Johannes R. (2015). De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy. Nature Genet., 47 (4). S. 393 - 402. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1546-1718

Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Muller, Juliane S., Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie ORCID: 0000-0003-4900-9877, Santorelli, Filippo M., Alfares, Ahmed A., Zhu, Changlian, Meszarosova, Anna Uhrova, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R., Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T., Strom, Tim M., De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana ORCID: 0000-0001-8939-1447, Alfadhel, Majid, van de Warrenburg, Bart P., Portier, Ruben, Bergmann, Carsten, Firouzabadi, Saghar Ghasemi, Jin, Sheng Chih ORCID: 0000-0002-5777-7262, Bilguvar, Kaya, Hamed, Sherifa ORCID: 0000-0002-1441-3530, Abdelhameed, Mohammed, Haridy, Nourelhoda A., Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair, Wood, Nick W., Mau-Them, Frederic Tran, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele ORCID: 0000-0003-4788-9719, Zara, Federico ORCID: 0000-0001-9744-5222, Salpietro, Vincenzo, Scala, Marcello ORCID: 0000-0003-2194-7239, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laetitia, Schmitt, Emmanuelle, Lacaze, Elodie, Kupper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J. H., Grand, Katheryn, Graham, John M., Lewis, Richard A., Millan, Francisca, Duman, Ozgur, Dundar, Nihal, Uyanik, Gokhan, Schols, Ludger ORCID: 0000-0001-7774-5025, Nurnberg, Peter, Nurnberg, Gudrun, Bordes, Andrea Catala, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Boucanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S., Shamseldin, Hanan, Al Tala, Saeed, Varaghchi, Jamileh Rezazadeh, Najafi, Maryam, Deschner, Selina, Glaser, Dieter, Huttel, Wolfgang, Kruer, Michael C., Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Zuchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schuele, Rebecca, Horvath, Rita ORCID: 0000-0002-9841-170X, Houlden, Henry, Bartesaghi, Luca ORCID: 0000-0001-8218-4648, Lee, Hwei-Jen, Ampatzis, Konstantinos, Pierson, Tyler Mark ORCID: 0000-0003-1985-3671 and Senderek, Jan (2021). Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. Brain, 144 (5). S. 1422 - 1435. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Muller, Juliane S., Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie ORCID: 0000-0003-4900-9877, Santorelli, Filippo M., Alfares, Ahmed A., Zhu, Changlian, Meszarosova, Anna Uhrova, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R., Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T., Strom, Tim M., De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana ORCID: 0000-0001-8939-1447, Alfadhel, Majid, van de Warrenburg, Bart P., Portier, Ruben, Bergmann, Carsten, Firouzabadi, Saghar Ghasemi, Jin, Sheng Chih ORCID: 0000-0002-5777-7262, Bilguvar, Kaya, Hamed, Sherifa ORCID: 0000-0002-1441-3530, Abdelhameed, Mohammed, Haridy, Nourelhoda A., Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair, Wood, Nick W., Mau-Them, Frederic Tran, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele ORCID: 0000-0003-4788-9719, Zara, Federico ORCID: 0000-0001-9744-5222, Salpietro, Vincenzo, Scala, Marcello ORCID: 0000-0003-2194-7239, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laetitia, Schmitt, Emmanuelle, Lacaze, Elodie, Kuepper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J. H., Grand, Katheryn, Graham, John M., Jr., Lewis, Richard A., Millan, Francisca, Duman, Ozgur, Dundar, Nihal, Uyanik, Gokhan, Schols, Ludger ORCID: 0000-0001-7774-5025, Nuernberg, Peter, Nuernberg, Gudrun, Bordes, Andrea Catala, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Boucanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S., Shamseldin, Hanan, Al Tala, Saeed, Varaghchi, Jamileh Rezazadeh, Najafi, Maryam, Deschner, Selina, Glaeser, Dieter, Huettel, Wolfgang, Kruer, Michael C., Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Zuchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schuele, Rebecca, Horvath, Rita ORCID: 0000-0002-9841-170X, Houlden, Henry, Bartesaghi, Luca ORCID: 0000-0001-8218-4648, Lee, Hwei-Jen, Ampatzis, Konstantinos, Pierson, Tyler Mark ORCID: 0000-0003-1985-3671 and Senderek, Jan (2021). Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. Brain, 144. S. 1422 - 1435. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

van der Zee, Julie, Gijselinck, Ilse, Van Mossevelde, Sara, Perrone, Federica ORCID: 0000-0002-4079-8972, Dillen, Lubina, Heeman, Bavo, Baumer, Veerle, Engelborghs, Sebastiaan, De Bleecker, Jan, Baets, Jonathan, Gelpi, Ellen, Rojas-Garcia, Ricardo, Clarimon, Jordi, Lleo, Alberto, Diehl-Schmid, Janine ORCID: 0000-0002-7745-1382, Alexopoulos, Panagiotis, Perneczky, Robert ORCID: 0000-0003-1981-7435, Synofzik, Matthis, Just, Jennifer, Schoels, Ludger, Graff, Caroline, Thonberg, Hakan, Borroni, Barbara, Padovani, Alessandro, Jordanova, Albena ORCID: 0000-0002-3833-3754, Sarafov, Stayko, Tournev, Ivailo, de Mendonca, Alexandre ORCID: 0000-0002-0488-1453, Miltenberger-Miltenyi, Gabriel ORCID: 0000-0003-0224-1281, Simoes do Couto, Frederico, Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Jessen, Frank, Heneka, Michael T., Gomez-Tortosa, Estrella, Danek, Adrian ORCID: 0000-0001-8857-5383, Cras, Patrick, Vandenberghe, Rik ORCID: 0000-0001-6237-2502, De Jonghe, Peter, De Deyn, Peter P., Sleegers, Kristel, Cruts, Marc and Van Broeckhoven, Christine ORCID: 0000-0003-0183-7665 (2017). TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis. Hum. Mutat., 38 (3). S. 297 - 310. HOBOKEN: WILEY. ISSN 1098-1004

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