Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Franziska Keidel"'
Autor:
Christian Matthias Zobel, Werner Wenzel, Jan Philipp Krüger, Ulrich Baumgarten, Tobias Wagelöhner, Nino Neumann, Behruz Foroutan, Rico Müller, Annette Müller, Dominic Rauschning, Meike Schüßler, Lorenz Scheit, Felix Weinreich, Klaas Oltmanns, Franziska Keidel, Maria Koch, Sebastian Spethmann, Maximilian Schreiner
Publikováno v:
Frontiers in Microbiology, Vol 14 (2023)
BackgroundCOVID-19 can show a variable course, from asymptomatic infections to acute respiratory failure and death. For efficient allocation of resources, patients should be stratified according to their risk for a severe course as early as possible.
Externí odkaz:
https://doaj.org/article/45713d4d5878410f98b1f739dcb42f63
Autor:
Hans-Peter Müller, Armin M. Nagel, Franziska Keidel, Arthur Wunderlich, Annemarie Hübers, Lena V. Gast, Albert C. Ludolph, Meinrad Beer, Jan Kassubek
Publikováno v:
Therapeutic Advances in Chronic Disease, Vol 13 (2022)
Objectives: Multiparametric magnetic resonance imaging (MRI) is established as a technical instrument for the characterisation of patients with amyotrophic lateral sclerosis (ALS). The contribution of relaxation-weighted sodium ( 23 NaR) MRI remains
Externí odkaz:
https://doaj.org/article/209b8548a1064300abd7c2b1c38abf56
Autor:
Leonie Franziska Keidel, Benedikt Schworm, Katharina Hohenfellner, Franziska Kruse, Siegfried Priglinger, Nikolaus Luft, Claudia Priglinger
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 240:266-275
Cystinosis is a rare lysosomal storage disease with a prevalence of 1:100.000-1:200.000 cases. It is caused by biallelic mutations in the CTNS gene, which encodes cystinosin that transports cystine out of lysosomes. Due to its dysfunction cystine cry
Autor:
Franziska Kruse, Leonie Franziska Keidel, Siegfried Priglinger, Nikolaus Luft, Claudia Priglinger
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 240:260-265
Nephropathic cystinosis is a rare autosomal recessive disease caused by mutations in the CTNS gene. This causes dysfunction of cystinosin, a protein that transports cystine out of lysosomes, causing cystine crystals to accumulate in cells in most org
Autor:
Hans-Peter, Müller, Armin M, Nagel, Franziska, Keidel, Arthur, Wunderlich, Annemarie, Hübers, Lena V, Gast, Albert C, Ludolph, Meinrad, Beer, Jan, Kassubek
Publikováno v:
Therapeutic advances in chronic disease. 13
Multiparametric magnetic resonance imaging (MRI) is established as a technical instrument for the characterisation of patients with amyotrophic lateral sclerosis (ALS). The contribution of relaxation-weighted sodium (Seventeen patients with ALS (mean
Autor:
Hans-Peter Müller, Armin M. Nagel, Franziska Keidel, Arthur Wunderlich, Annemarie Hübers, Lena V. Gast, Albert C. Ludolph, Meinrad Beer, Jan Kassubek
Publikováno v:
Therapeutic advances in chronic disease 13, 1-8 (2022). doi:10.1177/20406223221109480
Objectives: Multiparametric magnetic resonance imaging (MRI) is established as a technical instrument for the characterisation of patients with amyotrophic lateral sclerosis (ALS). The contribution of relaxation-weighted sodium (23NaR) MRI remains to