Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fiona Jäger"'
Autor:
Matthias Tomschik, Eva Renaud, Fiona Jäger, Chiara Paternostro, Jakob Rath, Walter Rinner, Gudrun Zulehner, Fritz Zimprich, Hakan Cetin
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract Repetitive nerve stimulation (RNS) is a standard test for the diagnosis of myasthenia gravis (MG), where decrement of compound muscle action potentials (CMAP) corresponds to clinical muscle fatigability. Our aim was to ascertain the diagnost
Externí odkaz:
https://doaj.org/article/776e5a00a402476090d1e7f830014146
Autor:
Martin Krenn, Matthias Tomschik, Matias Wagner, Gudrun Zulehner, Rosa Weng, Jakob Rath, Sigrid Klotz, Ellen Gelpi, Gabriel Bsteh, Omar Keritam, Isabella Colonna, Chiara Paternostro, Fiona Jäger, Elisabeth Lindeck‐Pozza, Stephan Iglseder, Susanne Grinzinger, Martina Schönfelder, Christina Hohenwarter, Manfred Freimüller, Norbert Embacher, Julia Wanschitz, Raffi Topakian, Ana Töpf, Volker Straub, Stefan Quasthoff, Fritz Zimprich, Wolfgang N. Löscher, Hakan Cetin
Publikováno v:
Eur. J. Neurol. 29, 1815-1824 (2022)
Hereditary myopathies with limb-girdle muscular weakness (LGW) are a genetically heterogeneous group of disorders, in which molecular diagnosis remains challenging. Our aim was to present a detailed clinical and genetic characterization of a large co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d69fd628f4b40ca99a78490f29f9ef5c
https://doi.org/10.1111/ene.15306
https://doi.org/10.1111/ene.15306
Incidence and clinical spectrum of rhabdomyolysis in general neurology: a retrospective cohort study
Autor:
Jakob Rath, Karl Bointner, Hakan Cetin, Rosa Weng, Lorina Gopp, Fiona Jäger, Thomas Berger, Fritz Zimprich, Chiara Paternostro, Martin Krenn, Gudrun Zulehner, Matthias Tomschik
Publikováno v:
Neuromuscular Disorders. 31:1227-1234
The objective of this retrospective cohort study was to evaluate demographic, clinical and laboratory characteristics of patients with rhabdomyolysis as defined by a serum creatine kinase (sCK) activity > 950 U/L. A total of 248 patients were recruit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::415ee5799d0357c8f86ce3dd0e3aa2b5
https://doi.org/10.1016/j.nmd.2021.09.012
https://doi.org/10.1016/j.nmd.2021.09.012
Autor:
Luca Cambioli, Dietmar Winkler, Arkadiusz Komorowski, Michaela-Elena Friedrich, Edda Pjrek, Siegfried Kasper, Markus Dold, Fiona Jäger, Rupert Lanzenberger
Publikováno v:
Psychotherapy and Psychosomatics. 89:17-24
Background: Bright light therapy (BLT) has been used as a treatment for seasonal affective disorder (SAD) for over 30 years. This meta-analysis was aimed to assess the efficacy of BLT in the treatment of SAD in adults. Method: We performed a systemat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a71b01c7bef1700c733fe033523e6ab
https://doi.org/10.1159/000502891
https://doi.org/10.1159/000502891
Publikováno v:
Journal of Neurology. 269:1026-1027
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32a49a6fd4775820f9f7e2942e45bcec
https://doi.org/10.1007/s00415-021-10769-2
https://doi.org/10.1007/s00415-021-10769-2
Publikováno v:
Journal of Visualized Experiments.
Vestibular disorders are among the most common syndromes in medicine. In recent years, new vestibular diagnostic systems have been introduced that allow the examination of all semicircular canals in the clinical setting. Assessment methods of the oto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::007f0c228bc474131d359a4499e66843
https://doi.org/10.3791/60418-v
https://doi.org/10.3791/60418-v
Autor:
Peter Aichele, Michele Proietti, Manfred W. Kilimann, Fiona Jäger, Sophie Jung, Bodo Grimbacher, Julika Neumann, Tamara Kögl, Fabio Grassi, Lisa Perruzza, Felicitas Felber, Pauline Soulas-Sprauel, Laura Gámez-Díaz
Publikováno v:
Immunology and Cell Biology
Immunology and Cell Biology, Nature Publishing Group, 2017, 95 (9), pp.789-802. ⟨10.1038/icb.2017.52⟩
Immunology and Cell Biology, Nature Publishing Group, 2017, 95 (9), pp.789-802. ⟨10.1038/icb.2017.52⟩
Biallelic mutations in the human lipopolysaccharide responsive beige-like anchor (LRBA) gene lead to a primary immunodeficiency known as LRBA deficiency, characterized by a broad range of clinical manifestations including autoimmunity, organomegaly,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97cb6ef077e84d68181889b3daaca218
https://hal.archives-ouvertes.fr/hal-03415531
https://hal.archives-ouvertes.fr/hal-03415531
