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Cerebellar Bottom of Fissure Hyperintensities in …
pub.dzne.de
Benjamin Roeben, MD ,1,2 Eva Bültmann, MD,3 Claudia Stendel, MD ,4,5 and Matthis Synofzik, MD 1,2 MT-ATP6-associated disease is caused by mutations in the mitochondrial gene MT …
Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A …
opus.bibliothek.uni-wuerzburg.de
Moritz Metelmann 15, Zacharias Kohl 16, Ralf A. Linker 16, Jan Christoph Koch 17, Claudia Stendel 18,19, Lars H. Müschen 1, Alma Osmanovic 1, Camilla Binz 1, Thomas Klopstock …
Progression Characteristics in Friedreich's Ataxia: A 4-Year ...SSRN eLibrary
papers.ssrn.com
von K Reetz — Claudia Stendel. Ludwig Maximilian University of Munich (LMU) - The Friedrich-Baur-Institute. Francisco Javier Rodríguez de Rivera Garrido. La ...
Cerebellar Bottom of Fissure Hyperintensities in MT‐ATP6 ...Wiley Online Library
onlinelibrary.wiley.com
von B Roeben · · Zitiert von: 1 — ... Claudia Stendel MD,. Claudia Stendel MD. orcid.org Department of Neurology, Friedrich-Baur-Institute, Ludwig-Maximilians ...
Association of A Novel Splice Site Mutation in P/Q-Type ...Semantic Scholar
pdfs.semanticscholar.org
von C Stendel · · Zitiert von: 13 — Claudia Stendel 1,2,†, Maria Cristina D'Adamo 3,†, Manuela Wiessner 1, Marina Dusl 1,. Marta Cenciarini 4, Silvia Belia 5, ... von P Schischlevskij · · Zitiert von: 16 — Ralf A. Linker 16, Jan Christoph Koch 17, Claudia Stendel 18,19,. Lars H. Müschen 1, Alma Osmanovic 1. , Camilla Binz 1, Thomas Klopstock
Longitudinal changes of SARA scale in Friedreich ataxia ...Wiley Online Library
onlinelibrary.wiley.com
von L Porcu · — ... Claudia Stendel,. Claudia Stendel. orcid.org Department of Neurology, Friedrich Baur Institute, University Hospital, LMU ...
International Paediatric Mitochondrial Disease ScaleNewcastle University
eprints.ncl.ac.uk
von S Koene · · Zitiert von: 18 — Dr. I. (René) F.M. de Coo reports no disclosures. Dr. Katharina Vill reports no disclosures. Dr. Claudia Stendel reports no disclosures.
MT‐ATP6 mitochondrial disease variantscnjournals.com
cnjournals.com
Authors: Rebecca D Ganetzky Claudia Stendel Elizabeth M McCormick Zarazuela Zolkipli‐Cunningham Amy C Goldstein Thomas Klopstock Marni J Falk.
Myelin is dependent on the Charcot-Marie-Tooth Type 4H ...ETH Zürich
www.research-collection.ethz.ch
von M Horn · · Zitiert von: 66 — Christian Somandin,1,* Hans Welzl,2 Claudia Stendel,1,† Tessa Lu¨hmann,3,z Carsten Wessig,4. Klaus V. Toyka,4,§ Joa˜o B. Relvas,1,5 Jan Senderek1,ô and Ueli ...
Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS)ProQuest
search.proquest.com
von P Schischlevskij · · Zitiert von: 30 — (Claudia Stendel), L.H.M., A.O., C.B., J.D., M.B., T.H., M.D., P.L., S.P., O.S.-K.; Validation—R.G., D.Z.,. C.S. (Carsten Schröter), U.W., M.R., J.W., I.S. ...
SIL1 mutations and clinical spectrum in patients with ...Oxford University Press
academic.oup.com
von M Krieger · · Zitiert von: 75 — Claudia Stendel,. Claudia Stendel. 33 Department of Neurology and JARA Brain Translational Medicine, RWTH Aachen, Aachen University, Germany.
SIL1 mutations and clinical spectrum in patients with ...Rero.ch
doc.rero.ch
von M Krieger · · Zitiert von: 75 — Michael Krieger,1 Andreas Roos,2 Claudia Stendel,3 Kristl G. Claeys,2,3 Fatma Mujgan Sonmez,4. Michael Baudis,5,6 Peter Bauer,7 Antje Bornemann,8 Christian ...
Symposium für Patienten mit primären mitochondrialenDeutsche Gesellschaft für Muskelkranke e.V.
www.dgm.org
Dr. Claudia Stendel. Neue Therapien und Aussichten,. München. Alltagsbewältigung und symptomatische. Therapien bei Erwachsenen, (kurz Mito und Covid 19).
AGENDA Klinisch-chemisches Kolloquium FS Universitätsspital Zürich
www.fortbildung.usz.ch
— Fr. Dr. Claudia Stendel. Zellbiology, ETH Zurich. (6.4. fällt aus:Ostern). Rare forms of inherited neuropathies provide insights into.
PLEKHG5 deficiency leads to an intermediate form of ...Europe PMC
europepmc.org
... Claudia Stendel. 7Department of Neurology, University Hospital RWTH Aachen, Aachen, Germany. Find articles by Claudia Stendel. Andreas Roos. 6Institute of ...
Mitochondrial diseases of the brainthe European Academy of Neurology
www.ean.org
— Claudia Stendel. Oskar Mikazans. University of Pisa. Michelangelo Mancuso. Dept. of Ophthalmology. Claudia Priglinger. University of Prague.
SH3TC2/KIAA1985 protein is required for proper myelination and the...
www.scienceopen.com
Authors: Claudia Stendel, Jennifer Zenker, Joachim Weis, Roman Chrast, E. Arnaud, Andreas Roos, Bernhard Lüscher, Anne-Laure Charles, ...
SH3TC2, a protein mutant in Charcot–Marie–Tooth ...Oxford Academic
academic.oup.com
von C Stendel · · Zitiert von: 96 — SH3TC2, a protein mutant in Charcot–Marie–Tooth neuropathy, links peripheral nerve myelination to endosomal recycling. Claudia Stendel ,. Claudia Stendel
Transcriptional regulator PRDM12 is essential for human pain...
www.scienceopen.com
... Diego Pereira, Carlos M Restrepo, Istvan Katona, Marina Dusl, Claudia Stendel, Thomas Wieland, Fay Stafford, Frank Reimann, Katja von Au, Christian Finke, ...
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