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pro vyhledávání: '"Schell, Nathalie"'
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Autor:
Lange, Lara M.1,2 (AUTHOR), Schell, Nathalie1,3 (AUTHOR), Tunc, Sinem1,2,4 (AUTHOR), Shoukier, Moneef5 (AUTHOR), Weißbach, Anne1,2,4 (AUTHOR), Hellenbroich, Yorck6 (AUTHOR), Brüggemann, Norbert1,2,7 (AUTHOR) norbert.brueggemann@neuro.uni-luebeck.de
Publikováno v:
Movement Disorders Clinical Practice. Nov2022, Vol. 9 Issue 8, p1116-1119. 4p.
Autor:
Usnich, Tatiana, Olmedillas, Maria, Schell, Nathalie, Paul, Jefri J., Curado, Filipa, Skobalj, Snezana, Csoti, Ilona, Ertan, Sibel, Gruber, Doreen, Zittel, Simone, Sammler, Esther, Isaacson, Stuart H., Kühn, Andrea A., Pedrosa, David J., Reetz, Kathrin, Kasten, Meike, Rolfs, Arndt, Bauer, Peter, Skrahina, Volha, Klein, Christine, Brüggemann, Norbert
Publikováno v:
In Parkinsonism and Related Disorders February 2023 107
Autor:
Usnich, Tatiana, Hauptmann, Björn, Hanssen, Henrike, Prasuhn, Jannik, Balck, Alexander, Borsche, Max, Tadic, Vera, Klee, Annika, Noblejas-Sanchez, Greta, Vollstedt, Eva-Juliane, Klein, Christine, Brüggemann, Norbert, Kasten, Meike, Graf, Julia, Schell, Nathalie, Modreanu, Raluca, Staemmler, Barbara, Loewin, Elena
Publikováno v:
NPJ Parkinson's Disease; 7/14/2023, Vol. 9 Issue 1, p1-5, 5p
Autor:
Usnich, Tatiana, Vollstedt, Eva-Juliane, Schell, Nathalie, Skrahina, Volha, Bogdanovic, Xenia, Gaber, Hanaa, Förster, Toni M., Heuer, Andreas, Koleva-Alazeh, Natalia, Csoti, Ilona, Basak, Ayse Nazli, Ertan, Sibel, Genc, Gencer, Bauer, Peter, Lohmann, Katja, Grünewald, Anne, Schymanski, Emma, Trinh, Joanne, Schaake, Susen, Berg, Daniela, Gruber, Doreen, Isaacson, Stuart H., Kühn, Andrea A., Mollenhauer, Brit, Pedrosa, David J., Reetz, Kathrin, Sammler, Esther M., Valente, Enza Maria, Valzania, Franco, Volkmann, Jens, Zittel, Simone, Brüggemann, Norbert, Kasten, Meike, Rolfs, Arndt, Klein, Christine, Group, The Lipad Study
Background: Pathogenic variants in the Leucine-rich repeat kinase 2 ( LRRK2) gene are the most common known monogenic cause of Parkinson's disease (PD). LRRK2 -linked PD is clinically indistinguishable from idiopathic PD and inherited in an autosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2658::857d6a8bbdb6d83701adee1b1e1fbf4f
http://orbilu.uni.lu/handle/10993/47999
http://orbilu.uni.lu/handle/10993/47999
Autor:
Vollstedt, Eva‐Juliane, Warrlich, Elena, Hauptmann, Björn, Hanssen, Henrike, Klein, Christine, Kasten, Meike, Balck, Alexander, Borsche, Max, Brüggemann, Norbert, Graf, Julia, Prasuhn, Jannik, Schell, Nathalie, Tadic, Vera, Usnich, Tatiana, Modreanu, Raluca
Publikováno v:
European Journal of Neurology; Jun2021, Vol. 28 Issue 6, pe35-e36, 2p
Publikováno v:
Journal of Parkinson's Disease. 2023 Supplement, Vol. 13, p1-414. 414p.
Autor:
Tatiana Usnich, Eva-Juliane Vollstedt, Nathalie Schell, Volha Skrahina, Xenia Bogdanovic, Hanaa Gaber, Toni M. Förster, Andreas Heuer, Natalia Koleva-Alazeh, Ilona Csoti, Ayse Nazli Basak, Sibel Ertan, Gencer Genc, Peter Bauer, Katja Lohmann, Anne Grünewald, Emma L. Schymanski, Joanne Trinh, Susen Schaake, Daniela Berg, Doreen Gruber, Stuart H. Isaacson, Andrea A. Kühn, Brit Mollenhauer, David J. Pedrosa, Kathrin Reetz, Esther M. Sammler, Enza Maria Valente, Franco Valzania, Jens Volkmann, Simone Zittel, Norbert Brüggemann, Meike Kasten, Arndt Rolfs, Christine Klein, The LIPAD Study Group
Publikováno v:
Frontiers in Neurology
Frontiers in Neurology, Vol 12 (2021)
Frontiers in neurology 12, 710572 (2021). doi:10.3389/fneur.2021.710572 special issue: "Neurogenetics / Huifang Shang, Speciality Chief Editor; Yan Asmann, Associate Editor; Peter O. Bauer, Associate Editor; Giorgio B. Boncoraglio, Associate Editor"
Frontiers in Neurology, Vol 12 (2021)
Frontiers in neurology 12, 710572 (2021). doi:10.3389/fneur.2021.710572 special issue: "Neurogenetics / Huifang Shang, Speciality Chief Editor; Yan Asmann, Associate Editor; Peter O. Bauer, Associate Editor; Giorgio B. Boncoraglio, Associate Editor"
Background: pathogenic variants in the Leucine-rich repeat kinase 2 (LRRK2) gene are the most common known monogenic cause of Parkinson's disease (PD). LRRK2-linked PD is clinically indistinguishable from idiopathic PD and inherited in an autosomal d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9086c827a9ae6ef75b271dbd13b7e586
Autor:
Schell, Johanna, Casas, Nathalie, Blom, Richard, Spjelkavik, Aud, Andersen, Anne, Cavka, Jasmina, Mazzotti, Marco
Publikováno v:
Adsorption; Nov2012, Vol. 18 Issue 3/4, p213-227, 15p
Publikováno v:
Adsorption; Feb2012, Vol. 18 Issue 1, p49-65, 17p