Хайлтын үр дүнгүүд - Tim W. Rattay
- 6-н 1 - 6 үр дүнгүүдийг харуулж байна
-
1
In-vivo evidence that high mobility group box 1 exerts deleterious effects in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model and Parkinson's disease which can be attenuated... -н Matteo Santoro, Walter Maetzler, Petros Stathakos, Heather L. Martin, Markus A. Hobert, Tim W. Rattay, Thomas Gasser, John V. Forrester, Daniela Berg, Kevin J. Tracey, Gernot Riedel, Peter Teismann
Хэвлэсэн 2016Artigo -
2
Nerve Ultrasound Predicts Treatment Response in Chronic Inflammatory Demyelinating Polyradiculoneuropathy—a Prospective Follow-Up -н Florian Härtig, Marlene Ross, Nele Dammeier, Nadin Fedtke, Bianka Heiling, Hubertus Axer, Bernhard F. Décard, Eva Auffenberg, Marilin Koch, Tim W. Rattay, Markus Krumbholz, Antje Bornemann, Holger Lerche, Natalie Winter, Alexander Grimm
Хэвлэсэн 2018Artigo -
3
Defining diagnostic cutoffs in neurological patients for serum very long chain fatty acids (VLCFA) in genetically confirmed X-Adrenoleukodystrophy -н Tim W. Rattay, Maren Rautenberg, Anne S. Söhn, Holger Hengel, Andreas Traschütz, Benjamin Röben, Stefanie N. Hayer, Rebecca Schüle, Sarah Wiethoff, Lena Zeltner, Tobias B. Haack, Alexander Čegan, Lüdger Schöls, Erwin Schleicher, Andreas Peter
Хэвлэсэн 2020Artigo -
4
FAHN/SPG35: a narrow phenotypic spectrum across disease classifications -н Tim W. Rattay, Tobias Lindig, Jonathan Baets, Katrien Smets, Tine Deconinck, Anne S. Söhn, Konstanze Hörtnagel, Kathrin N. Eckstein, Sarah Wiethoff, Jennifer Reichbauer, Marion Döbler‐Neumann, Ingeborg Krägeloh‐Mann, Michaela Auer‐Grumbach, Barbara Plecko, Alexander Münchau, Bernd Wilken, Marc Janauschek, Anne‐Katrin Giese, Jan De Bleecker, Els Ortibus, Martine Debyser, Adolfo López de Munaín, Aurora Pujol, Maria Teresa Bassi, Maria Grazia D’Angelo, Peter De Jonghe, Stephan Züchner, Peter Bauer, Lüdger Schöls, Rebecca Schüle
Хэвлэсэн 2019Artigo -
5
Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial -н Lüdger Schöls, Tim W. Rattay, Peter Martus, Christoph Meisner, Jonathan Baets, Imma Fischer, Christine Jägle, Matthew J. Fraidakis, Andrea Martinuzzi, Jonas Alex Morales Saute, Marina Scarlato, Antonella Antenora, Claudia Stendel, Philip Höflinger, Charles Marques Lourenço, Lisa Abreu, Katrien Smets, Martin Paucar, Tine Deconinck, Dana M. Bis‐Brewer, Sarah Wiethoff, Peter Bauer, Alessia Arnoldi, Wilson Marques, Laura Bannach Jardim, Stefan Hauser, Chiara Criscuolo, Alessandro Filla, Stephan Züchner, Maria Teresa Bassi, Thomas Klopstock, Peter De Jonghe, Ingemar Björkhem, Rebecca Schüle
Хэвлэсэн 2017Artigo -
6
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia -н Martina Minnerop, Delia Kurzwelly, Holger Wagner, Anne S. Soehn, Jennifer Reichbauer, Feifei Tao, Tim W. Rattay, Michael Peitz, Kristina Rehbach, Alejandro Giorgetti, Angela Pyle, Holger Thiele, Janine Altmüller, Dagmar Timmann, Ilker Karaca, Martina Lennarz, Jonathan Baets, Holger Hengel, Matthis Synofzik, Burcu Atasu, Shawna Feely, Marina Kennerson, Claudia Stendel, Tobias Lindig, Michael Gonzalez, Rüdiger Stirnberg, Marc Sturm, Sandra Roeske, Johanna Jung, Peter Bauer, Ebba Lohmann, Stefan Herms, Stefanie Heilmann‐Heimbach, Garth A. Nicholson, Muhammad Mahanjah, Rajech Sharkia, Paolo Carloni, Oliver Brüstle, Thomas Klopstock, Katherine D. Mathews, Michael E. Shy, Peter De Jonghe, Patrick F. Chinnery, Rita Horváth, Jürgen Kohlhase, Ina Schmitt, Michael Wolf, Susanne Greschus, Katrin Amunts, Wolfgang Maier, Lüdger Schöls, Peter Nürnberg, Stephan Züchner, Thomas Klockgether, Alfredo Ramı́rez, Rebecca Schüle
Хэвлэсэн 2017Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Medicine
Biology
Disease
Endocrinology
Gene
Internal medicine
Pathology
Phenotype
Psychiatry
Gastroenterology
Genetics
Hereditary spastic paraplegia
Immunology
Neurodegeneration
Adrenoleukodystrophy
Ataxia
Biochemistry
Cerebellar ataxia
Chemistry
Cholesterol
Compound heterozygosity
Dopamine
Dopaminergic
Guillain-Barre syndrome
HMGB1
Histology
Inflammation
MPTP
Microglia
Missense mutation