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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 22
2024
Wiesenfarth, Maximilian; Dorst, Johannes; Brenner, David; Elmas, Zeynep; Parlak, Oezlem; Uzelac, Zeljko; Kandler, Katharina; Mayer, Kristina; Weiland, Ulrike; Herrmann, Christine; Schuster, Joachim; Freischmidt, Axel; Mueller, Kathrin; Siebert, Reiner; Bachhuber, Franziska; Simak, Tatiana; Guenther, Kornelia; Froehlich, Elke; Knehr, Antje; Regensburger, Martin; German, Alexander; Petri, Susanne; Grosskreutz, Julian; Klopstock, Thomas; Reilich, Peter; Schoeberl, Florian; Hagenacker, Tim; Weyen, Ute; Guenther, Rene; Vidovic, Maximilian; Jentsch, Martin; Haarmeier, Thomas; Weydt, Patrick; Valkadinov, Ivan; Hesebeck-Brinckmann, Jasper; Conrad, Julian; Weishaupt, Jochen Hans; Schumann, Peggy; Koertvelyessy, Peter; Meyer, Thomas; Ruf, Wolfgang Philipp; Witzel, Simon; Senel, Makbule; Tumani, Hayrettin und Ludolph, Albert Christian
(2024):
Effects of tofersen treatment in patients with SOD1-ALS in a real-world setting - a 12-month multicenter cohort study from the German early access program.
In: Eclinicalmedicine, Bd. 69, 102495
[PDF, 1MB]
Reilich, Peter 
ORCID: https://orcid.org/0000-0002-2464-0681; Schöberl, Florian; Hiebeler, Miriam; Tonon, Matthias; Ludolph, Albert C. und Senel, Makbule
(2024):
Myelitis as a side effect of tofersen therapy in SOD1-associated ALS.
In: Journal of Neurology, Bd. 271, Nr. 4: S. 2114-2118
[PDF, 1MB]
ORCID: https://orcid.org/0000-0002-2464-0681; Schöberl, Florian; Hiebeler, Miriam; Tonon, Matthias; Ludolph, Albert C. und Senel, Makbule
(2024):
Myelitis as a side effect of tofersen therapy in SOD1-associated ALS.
In: Journal of Neurology, Bd. 271, Nr. 4: S. 2114-2118
[PDF, 1MB]
2023
Wiesenfarth, Maximilian; Guenther, Kornelia; Mueller, Kathrin; Witzel, Simon; Weiland, Ulrike; Mayer, Kristina; Herrmann, Christine; Brenner, David; Schuster, Joachim; Freischmidt, Axel; Lule, Dorothee; Meyer, Thomas; Regensburger, Martin; Grehl, Torsten; Emmer, Alexander; Petri, Susanne; Grosskreutz, Julian; Roediger, Annekathrin; Steinbach, Robert; Klopstock, Thomas; Reilich, Peter; Schoeberl, Florian; Wolf, Joachim; Hagenacker, Tim; Weyen, Ute; Zeller, Daniel; Ludolph, Albert C. und Dorst, Johannes
(2023):
Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations.
In: Brain Communications, Bd. 5, Nr. 2, fcad087
[PDF, 806kB]
2022
Schorling, Elisabeth; Senn, Katja C.; Thiele, Simone; Gumbert, Laura; Krause, Sabine; Schreiber-Katz, Olivia; Walter, Maggie C.; Reilich, Peter und Nagels, Klaus H.
(2022):
Health-related Quality of Life and Satisfaction with German Health Care Services in Patients with Charcot-Marie-Tooth Neuropathy.
In: Journal of Neuromuscular Diseases, Bd. 9, Nr. 1: S. 211-220
Erdmann, Hannes; Scharf, Florentine; Gehling, Stefanie; Benet-Pages, Anna; Jakubiczka, Sibylle; Becker, Kerstin; Seipelt, Maria; Kleefeld, Felix; Knop, Karl Christian; Prott, Eva Christina; Hiebeler, Miriam; Montagnese, Federica; Glaeser, Dieter; Vorgerd, Matthias; Hagenacker, Tim; Walter, Maggie C.; Reilich, Peter; Neuhann, Teresa; Zenker, Martin; Holinski-Feder, Elke; Schoser, Benedikt und Abicht, Angela
(2022):
Methylation of the 4q35 D4Z4 repeat defines disease status in facioscapulohumeral muscular dystrophy.
In: Brain, Bd. 146, Nr. 4: S. 1388-1402
Hiebeler, Miriam; Reinholz, Markus; Flaig, Michael; Schmidt, Christian; Schoser, Benedikt; Herzinger, Thomas; Abicht, Angela und Reilich, Peter
(2022):
Cutaneous T-cell lymphoma mimicking myopathy with lipoatrophy.
In: Neuromuscular Disorders, Bd. 32, Nr. 1: S. 65-70
2021
Reilich, Peter; Schlotter, Beate; Montagnese, Federica; Jordan, Berit; Stock, Friedrich; Schaeff-Vogelsang, Mario; Hotter, Benjamin; Eger, Katherina; Diebold, Isabel; Erdmann, Hannes; Becker, Kerstin; Schoen, Ulrike und Abicht, Angela
(2021):
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2P.
In: Neuromuscular Disorders, Bd. 31, Nr. 2: S. 123-133
Hiebeler, Miriam; Abicht, Angela; Reilich, Peter und Walter, Maggie C.
(2021):
Effect of Discontinuation of Nusinersen Treatment in Long-Standing SMA3.
In: Journal of Neuromuscular Diseases, Bd. 8, Nr. 4: S. 537-542
Schöberl, Florian; Abicht, Angela; Kuepper, Clemens; Voelk, Stefanie; Sonnenfeld, Stefan; Tonon, Matthias; Schaub, Annalisa; Scholz, Veronika; Kleinle, Stephanie; Erdmann, Hannes; Wolf, Dieter A. und Reilich, Peter
(2021):
Sensory neuropathy due to RFC1 in a patient with ALS: more than a coincidence?
In: Journal of neurology
[PDF, 488kB]
2019
Ikenberg, Elena; Reilich, Peter; Abicht, Angela; Heller, Corina; Schoser, Benedikt und Walter, Maggie C.
(2019):
Charcot-Marie-Tooth disease type 2CC due to a frameshift mutation of the neurofilament heavy polypeptide gene in an Austrian family.
In: Neuromuscular Disorders, Bd. 29, Nr. 5: S. 392-397
Schorling, Elisabeth; Thiele, Simone; Gumbert, Laura; Krause, Sabine; Klug, Constanze; Schreiber-Katz, Olivia; Reilich, Peter; Nagels, Klaus und Walter, Maggie C.
(2019):
Cost of illness in Charcot-Marie-Tooth neuropathy Results from Germany.
In: Neurology, Bd. 92, Nr. 17, E2027-E2037
Patzig, Maximilian; Bochmann, Katja; Lutz, Jürgen; Stahl, Robert; Kuepper, Clemens; Liebig, Thomas; Reilich, Peter und Dieterich, Marianne
(2019):
Measurement of structural integrity of the spinal cord in patients with amyotrophic lateral sclerosis using diffusion tensor magnetic resonance imaging.
In: PLOS One 14(10), e0224078 [PDF, 1MB]
In: PLOS One 14(10), e0224078 [PDF, 1MB]
2018
Walter, Maggie C. und Reilich, Peter
(2018):
Molekulare Therapien von Muskeldystrophien.
In: Fortschritte der Neurologie Psychiatrie, Bd. 86, Nr. 9: S. 535-542
2017
Ikenberg, Elena; Karin, Ivan; Ertl-Wagner, Birgit; Abicht, Angela; Bulst, Stefanie; Sabine, Krause; Schoser, Benedikt; Reilich, Peter und Walter, Maggie C.
(2017):
Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patient.
In: Neuromuscular Disorders, Bd. 27, Nr. 9: S. 856-860
Walter, Maggie C. und Reilich, Peter
(2017):
Recent developments in Duchenne muscular dystrophy: facts and numbers.
In: Journal of Cachexia Sarcopenia and Muscle, Bd. 8, Nr. 5: S. 681-685
2016
Lukacs, Zoltan; Cobos, Paulina Nieves; Wenninger, Stephan; Willis, Tracey A.; Guglieri, Michela; Roberts, Marc; Quinlivan, Rosaline; Hilton-Jones, David; Evangelista, Teresinha; Zierz, Stephan; Schlotter-Weigel, Beate; Walter, Maggie C.; Reilich, Peter; Klopstock, Thomas; Deschauer, Marcus; Straub, Volker; Müller-Felber, Wolfgang und Schoser, Benedikt
(2016):
Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weakness.
In: Neurology, Bd. 87, Nr. 3: S. 295-298
Klug, Constanze; Schreiber-Katz, Olivia; Thiele, Simone; Schorling, Elisabeth; Zowe, Janet; Reilich, Peter; Walter, Maggie C. und Nagels, Klaus H.
(2016):
Disease burden of spinal muscular atrophy in Germany.
In: Orphanet Journal of Rare Diseases
11:58
[PDF, 828kB]
2014
Schreiber-Katz, Olivia; Klug, Constanze; Thiele, Simone; Schorling, Elisabeth; Zowe, Janet; Reilich, Peter; Nagels, Klaus H. und Walter, Maggie C.
(2014):
Comparative cost of illness analysis and assessment of health care burden of Duchenne and Becker muscular dystrophies in Germany.
In: Orphanet Journal of Rare Diseases
9:210
[PDF, 909kB]
2013
Walter, Maggie C.; Reilich, Peter; Thiele, Simone; Schessl, Joachim; Schreiber, Herbert; Reiners, Karlheinz; Kress, Wolfram; Mueller-Reible, Clemens; Vorgerd, Matthias; Urban, Peter; Schrank, Bertold; Deschauer, Marcus; Schlotter-Weigel, Beate; Kohnen, Ralf und Lochmueller, Hanns
(2013):
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial.
In: Orphanet Journal of Rare Diseases
8:26
[PDF, 3MB]
2009
Stülpnagel, Celina von; Reilich, Peter; Straube, Andreas; Schäfer, Jan; Blaschek, Astrid; Lee, Seung-Hee; Müller-Felber, Wolfgang; Henschel, Volkmar; Mansmann, Ulrich und Heinen, Florian
(2009):
Myofascial Trigger Points in Children With Tension-Type Headache: A New Diagnostic and Therapeutic Option.
In: Journal of Child Neurology, Bd. 24, Nr. 4: S. 406-409
[PDF, 109kB]
Stülpnagel, Celina von; Reilich, Peter; Straube, Andreas; Schaefer, Jan; Blaschek, Astrid; Lee, Seung-Hee; Müller-Felber, Wolfgang; Henschel, Volkmar; Mansmann, Ulrich und Heinen, Florian
(2009):
Myofascial trigger points in children with tension-type headache: A new diagnostic and therapeutic option.
In: Journal of Child Neurology, Bd. 24, Nr. 4: S. 406-409
McNeill, Alisdair; Birchall, Daniel; Straub, Volker; Goldfarb, Lev; Reilich, Peter; Walter, Maggie C.; Schramm, Nicolai; Lochmueller, Hanns und Chinnery, Patrick F.
(2009):
Lower Limb Radiology of Distal Myopathy due to the S60F Myotilin Mutation.
In: European Neurology, Nr. 3: S. 161-166
[PDF, 198kB]