Miriam Matysik
Biographic Data
| ID | 7963336 |
|---|---|
| NAME | Miriam Matysik |
| GIVEN NAMES | Miriam |
| FAMILY NAME | Matysik |
| SIGNATURE | MATYSIK M |
| AFFILIATIONS | University of Freiburg |
| VERIFIED | No |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 2 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2020 |
| LATEST PUBLICATION YEAR | 2020 |
| H-INDEX | 0 |
Probable Autoimmune Depression in a Patient With Multiple Sclerosis and Antineuronal Antibodies
The present patient suffered from a probable "autoimmune depression" in the context of newly diagnosed multiple sclerosis with typical MRI and CSF pathologies, alongside mild concomitant latent systemic autoimmune process (with high-titer ANAs and lymphopenia) and unknown antineuronal antibodies. The case report illustrates that a depressive syndrome suggestive of primary idiopathic depressive disorder may be associated with an autoimmune brain i…
Anti-N-Methyl-D-Aspartate-Receptor Encephalitis
Anti-inflammatory treatment led to almost full recovery with persistent disappearance of catatonic symptoms; however, a dysexecutive syndrome led to ongoing relevant problems with good response to low-dose atypical neuroleptics and CBT. The patient had persistent EEG alterations that indicated continuing neuronal network instability. Therefore, the case demonstrates the importance of multidisciplinary outpatient treatment following acute therapy …
No prominent works on this page.
Probable Autoimmune Depression in a Patient With Multiple Sclerosis and Antineuronal Antibodies
The present patient suffered from a probable "autoimmune depression" in the context of newly diagnosed multiple sclerosis with typical MRI and CSF pathologies, alongside mild concomitant latent systemic autoimmune process (with high-titer ANAs and lymphopenia) and unknown antineuronal antibodies. The case report illustrates that a depressive syndrome suggestive of primary idiopathic depressive disorder may be associated with an autoimmune brain i…
Anti-N-Methyl-D-Aspartate-Receptor Encephalitis
Anti-inflammatory treatment led to almost full recovery with persistent disappearance of catatonic symptoms; however, a dysexecutive syndrome led to ongoing relevant problems with good response to low-dose atypical neuroleptics and CBT. The patient had persistent EEG alterations that indicated continuing neuronal network instability. Therefore, the case demonstrates the importance of multidisciplinary outpatient treatment following acute therapy …
Autoimmune Neurological Disorders and Treatments (2 works) · Immunology (2 works) · Medicine (2 works) · Peripheral Neuropathies and Disorders (2 works) · Amisulpride (1 works) · Anti-NMDA receptor encephalitis (1 works) · Anxiety (1 works) · Autoimmune encephalitis (1 works) · Context (archaeology (1 works) · Corpus callosum (1 works)