Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Emil Valizada"'
Autor:
Philipp Schwenkenbecher, Alexandra Neyazi, Frank Donnerstag, Felix C. Ringshausen, Roland Jacobs, Matthias Stoll, Philip Kirschner, Florian Peter Länger, Emil Valizada, Stefan Gingele, Florian Wegner, Kurt-Wolfram Sühs, Martin Stangel, Thomas Skripuletz
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Chronic granulomatous disease (CGD) is a rare genetic immunodeficiency, which is characterized by recurrent severe bacterial and fungal infections caused by a defect in phagocytic cells due to loss of superoxide production. The disease usually manife
Externí odkaz:
https://doaj.org/article/4a632b3a10db467f9aef5554d968fd1c
Anti–GABA-A Receptor Antibody-Mediated Epilepsia Partialis Continua After Treatment With Alemtuzumab
Autor:
Dominica Ratuszny, Thomas Skripuletz, Thomas Stüber, Emil Valizada, Klaus Gehring, Philipp Ertl, Jörg Andreas Müller, Mike P. Wattjes, Friedrich Feuerhake, Kurt-Wolfram Sühs
Publikováno v:
Neurology - Neuroimmunology Neuroinflammation. 10:e200123
Background and ObjectivesPatients with anti–GABA-A receptor encephalitis characteristically experience therapy-refractory epileptic seizures. General anesthesia is often required to terminate refractory status epilepticus. The immunologic mechanism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57f58d711a688599ad06b071387aa381
https://doi.org/10.1212/nxi.0000000000200123
https://doi.org/10.1212/nxi.0000000000200123
Autor:
Gisela Stoltenburg-Didinger, Dirk Fitzner, Stefan Nessler, Christian Hartmann, Caroline G. Bergner, Anne Winkler, Franziska van der Meer, Claudia Wrzos, Christine Stadelmann, Emil Valizada, Simon Hametner, Mevlude Türkmen, Wolfgang Brück, Sabine Pfeifenbring
Publikováno v:
Glia
X‐linked adrenoleukodystrophy (X‐ALD) and metachromatic leukodystrophy (MLD) are two relatively common examples of hereditary demyelinating diseases caused by a dysfunction of peroxisomal or lysosomal lipid degradation. In both conditions, accumu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2768b1fc357db3ee77acb5bc8a52e34f
http://europepmc.org/articles/PMC6594046
http://europepmc.org/articles/PMC6594046
Autor:
Florian Wegner, Felix C. Ringshausen, Thomas Skripuletz, Philipp Schwenkenbecher, Kurt-Wolfram Sühs, Alexandra Neyazi, Martin Stangel, Matthias Stoll, Philip Kirschner, Frank Donnerstag, Emil Valizada, Roland Jacobs, Florian Länger, Stefan Gingele
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Chronic granulomatous disease (CGD) is a rare genetic immunodeficiency which is characterized by recurrent severe bacterial and fungal infections caused by a defect in phagocytic cells due to loss of superoxide production. The disease usually manifes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3affe9d9740255a5ada03b49bb619d86
https://pubmed.ncbi.nlm.nih.gov/29915596
https://pubmed.ncbi.nlm.nih.gov/29915596