Browsing Universitätsbibliographie by Author "Rattay, Tim Wilfried"

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Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia

Kessler, Christoph; Serna-Higuita, Lina M.; Rattay, Tim W.; Maetzler, Walter; Wurster, Isabel; Hayer, Stefanie; Wilke, Carlo; Hengel, Holger; Reichbauer, Jennifer; Armbruster, Marcel; Schoels, Ludger; Martus, Peter; Schuele, Rebecca (2021)
Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4)

Rattay, Tim W.; Boldt, Andreas; Voelker, Maximilian; Wiethoff, Sarah; Hengel, Holger; Schuele, Rebecca; Schoels, Ludger (2020)
Peripheral nerve ultrasound scoring systems: benchmarking and comparative analysis

Grimm, Alexander; Rattay, Tim W.; Winter, Natalie; Axer, Hubertus (2017)
PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study

Gonsior, Kathrin; Kaucher, Gabriele Anna; Pelz, Patrik; Schumann, Dorothea; Gansel, Melanie; Kuhs, Sandra; Klockgether, Thomas; Forlani, Sylvie; Durr, Alexandra; Hauser, Stefan; Rattay, Tim W.; Synofzik, Matthis; Hengel, Holger; Schoels, Ludger; Riess, Olaf H.; Huebener-Schmid, Jeannette (2021)
Serum neurofilament light chain is increased in hereditary spastic paraplegias

Wilke, Carlo; Rattay, Tim W.; Hengel, Holger; Zimmermann, Milan; Brockmann, Kathrin; Schoels, Ludger; Kuhle, Jens; Schuele, Rebecca; Synofzik, Matthis (2018)
The prodromal phase of hereditary spastic paraplegia type 4: the preSPG4 cohort study

Rattay, Tim W.; Voelker, Maximilian; Rautenberg, Maren; Kessler, Christoph; Wurster, Isabel; Winter, Natalie; Haack, Tobias B.; Lindig, Tobias; Hengel, Holger; Synofzik, Matthis; Schule, Rebecca; Martus, Peter; Schoels, Ludger (2023)
Total tau is increased, but phosphorylated tau not decreased, in cerebrospinal fluid in amyotrophic lateral sclerosis

Wilke, Carlo; Deuschle, Christian; Rattay, Tim W.; Maetzler, Walter; Synofzik, Matthis (2015)
Ultrasound assessment of peripheral nerve pathology in neurofibromatosis type 1 and 2

Winter, Natalie; Rattay, Tim W.; Axer, Hubertus; Schaeffer, Eva; Decard, Bernhard F.; Gugel, Isabel; Schuhmann, Martin; Grimm, Alexander (2017)
Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxias

Bis, Dana M.; Schuele, Rebecca; Reichbauer, Jennifer; Synofzik, Matthis; Rattay, Tim W.; Soehn, Anne; de Jonghe, Peter; Schoels, Ludger; Zuchner, Stephan (2017)
Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families

Soehn, Anne S.; Rattay, Tim W.; Beck-Woedl, Stefanie; Schaeferhoff, Karin; Monk, David; Doebler-Neumann, Marion; Hoertnagel, Konstanze; Schluter, Agatha; Ruiz, Montserrat; Pujol, Aurora; Zuchner, Stephan; Riess, Olaf; Schule, Rebecca; Bauer, Peter; Schoels, Ludger (2016)

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