| Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial L Schöls, TW Rattay, P Martus, C Meisner, J Baets, I Fischer, C Jägle, ... Brain 140 (12), 3112-3127, 2017 | 105 | 2017 |
| Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia M Minnerop, D Kurzwelly, H Wagner, AS Soehn, J Reichbauer, F Tao, ... Brain 140 (6), 1561-1578, 2017 | 103 | 2017 |
| Nerve ultrasound predicts treatment response in chronic inflammatory demyelinating polyradiculoneuropathy—a prospective follow-up F Härtig, M Ross, NM Dammeier, N Fedtke, B Heiling, H Axer, BF Décard, ... Neurotherapeutics 15, 439-451, 2018 | 90 | 2018 |
| 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 … M Santoro, W Maetzler, P Stathakos, HL Martin, MA Hobert, TW Rattay, ... Neurobiology of disease 91, 59-68, 2016 | 81 | 2016 |
| FAHN/SPG35: a narrow phenotypic spectrum across disease classifications TW Rattay, T Lindig, J Baets, K Smets, T Deconinck, AS Söhn, ... Brain 142 (6), 1561-1572, 2019 | 66 | 2019 |
| Peripheral nerve ultrasound scoring systems: benchmarking and comparative analysis A Grimm, TW Rattay, N Winter, H Axer Journal of neurology 264, 243-253, 2017 | 54 | 2017 |
| A look inside the nerve–Morphology of nerve fascicles in healthy controls and patients with polyneuropathy A Grimm, N Winter, TW Rattay, F Härtig, NM Dammeier, E Auffenberg, ... Clinical Neurophysiology 128 (12), 2521-2526, 2017 | 51 | 2017 |
| Nerve ultrasound as follow‐up tool in treated multifocal motor neuropathy TW Rattay, N Winter, BF Décard, NM Dammeier, F Härtig, M Ceanga, ... European Journal of Neurology 24 (9), 1125-1134, 2017 | 49 | 2017 |
| Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations T Lindig, B Bender, TK Hauser, S Mang, D Schweikardt, U Klose, ... Journal of neurology 262, 1961-1971, 2015 | 42 | 2015 |
| GDF15/MIC1 and MMP9 cerebrospinal fluid levels in Parkinson’s disease and Lewy body dementia W Maetzler, W Deleersnijder, V Hanssens, A Bernard, K Brockmann, ... PloS one 11 (3), e0149349, 2016 | 40 | 2016 |
| Total tau is increased, but phosphorylated tau not decreased, in cerebrospinal fluid in amyotrophic lateral sclerosis C Wilke, C Deuschle, TW Rattay, W Maetzler, M Synofzik Neurobiology of aging 36 (2), 1072-1074, 2015 | 40 | 2015 |
| Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families AS Soehn, TW Rattay, S Beck-Wödl, K Schäferhoff, D Monk, ... Neurology 87 (2), 186-191, 2016 | 36 | 2016 |
| Ultrasound assessment of peripheral nerve pathology in neurofibromatosis type 1 and 2 N Winter, TW Rattay, H Axer, E Schäffer, BF Décard, I Gugel, ... Clinical Neurophysiology 128 (5), 702-706, 2017 | 32 | 2017 |
| Cognitive impairment in Glucocerebrosidase (GBA)‐associated PD: Not primarily associated with cerebrospinal fluid Abeta and Tau profiles S Lerche, C Schulte, K Srulijes, A Pilotto, TW Rattay, AK Hauser, ... Movement Disorders 32 (12), 1780-1783, 2017 | 29 | 2017 |
| Uniparental disomy determined by whole‐exome sequencing in a spectrum of rare motoneuron diseases and ataxias DM Bis, R Schüle, J Reichbauer, M Synofzik, TW Rattay, A Soehn, ... Molecular genetics & genomic medicine 5 (3), 280-286, 2017 | 29 | 2017 |
| Serum neurofilament light chain is increased in hereditary spastic paraplegias C Wilke, TW Rattay, H Hengel, M Zimmermann, K Brockmann, L Schöls, ... Annals of clinical and translational neurology 5 (7), 876-882, 2018 | 28 | 2018 |
| Face pareidolia in schizophrenia R Rolf, AN Sokolov, TW Rattay, AJ Fallgatter, MA Pavlova Schizophrenia research 218, 138-145, 2020 | 24 | 2020 |
| Cerebrospinal fluid findings in patients with psychotic symptoms—a retrospective analysis TW Rattay, P Martin, D Vittore, H Hengel, I Cebi, J Tünnerhoff, ... Scientific reports 11 (1), 1-12, 2021 | 21 | 2021 |
| Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4) TW Rattay, A Boldt, M Völker, S Wiethoff, H Hengel, R Schüle, L Schöls Journal of neurology 267, 369-379, 2020 | 21 | 2020 |
| PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study K Gonsior, GA Kaucher, P Pelz, D Schumann, M Gansel, S Kuhs, ... Journal of neurology 268, 1304-1315, 2021 | 20 | 2021 |
Rebecca SchüleDivision of Neurodegenerative Diseases and Movement Disorders, Dept. of Neurology, Univ Heidelberguni-heidelberg.de üzerinde doğrulanmış e-posta adresine sahip
