Currently, 12 cases (including our patient) of autoimmune encephalitis/encephalopathy after daclizumab therapy in MS are known worldwide and led to voluntary withdrawal of marketing authorization for daclizumab by the manufacturer Biogen (press release from European Medicines Agency, 07.03.2018). Our findings suggest that early recognition of DRESS even with CNS manifestations and swift treatment with steroids and/or plasma exchange are essential to improve the longterm outcome
Discontinuation of fingolimod in patients with multiple sclerosis (MS) can lead to disease reactivat...
Immune-mediated encephalitis as an adverse event due to checkpoint inhibitors is very rare. We descr...
Fingolimod (FTY) is a disease modifying therapy for relapsing remitting multiple sclerosis (RRMS) wh...
We provide clinical commentary on this edition's case report of immune-mediated encephalitis related...
BACKGROUND: Daclizumab is an anti-CD25 monoclonal antibody developed for the treatment of relapsing...
The US Food and Drug Administration (FDA) approved Zinbryta, an interleukin-2 receptor blocking anti...
INTRODUCTION: Cutaneous adverse events (AEs) have been observed in clinical studies of daclizumab hi...
Background Daclizumab is an anti-CD25 monoclonal antibody developed for the treatment of relapsing r...
Objective: SELECTED, an open-label extension study, evaluated daclizumab beta treatment for up to 6 ...
<p><b>Article full text</b></p> <p><br></p> <p>The full text of this article can be found here<b>....
Multiple sclerosis (MS) is a typical CD4 T cell-mediated autoimmune disease of the central nervous s...
Background: Interferon (IFN) beta drugs have been approved for the treatment of relapsing forms of...
INTRODUCTION: Neurological immune-related adverse events are a rare but potentially deadly complicat...
Background: Daclizumab is a humanized monoclonal antibody against the D-subunit (CD25) of the high-a...
The therapeutic options for disease modification in relapsing-remitting multiple sclerosis (RRMS) ha...
Discontinuation of fingolimod in patients with multiple sclerosis (MS) can lead to disease reactivat...
Immune-mediated encephalitis as an adverse event due to checkpoint inhibitors is very rare. We descr...
Fingolimod (FTY) is a disease modifying therapy for relapsing remitting multiple sclerosis (RRMS) wh...
We provide clinical commentary on this edition's case report of immune-mediated encephalitis related...
BACKGROUND: Daclizumab is an anti-CD25 monoclonal antibody developed for the treatment of relapsing...
The US Food and Drug Administration (FDA) approved Zinbryta, an interleukin-2 receptor blocking anti...
INTRODUCTION: Cutaneous adverse events (AEs) have been observed in clinical studies of daclizumab hi...
Background Daclizumab is an anti-CD25 monoclonal antibody developed for the treatment of relapsing r...
Objective: SELECTED, an open-label extension study, evaluated daclizumab beta treatment for up to 6 ...
<p><b>Article full text</b></p> <p><br></p> <p>The full text of this article can be found here<b>....
Multiple sclerosis (MS) is a typical CD4 T cell-mediated autoimmune disease of the central nervous s...
Background: Interferon (IFN) beta drugs have been approved for the treatment of relapsing forms of...
INTRODUCTION: Neurological immune-related adverse events are a rare but potentially deadly complicat...
Background: Daclizumab is a humanized monoclonal antibody against the D-subunit (CD25) of the high-a...
The therapeutic options for disease modification in relapsing-remitting multiple sclerosis (RRMS) ha...
Discontinuation of fingolimod in patients with multiple sclerosis (MS) can lead to disease reactivat...
Immune-mediated encephalitis as an adverse event due to checkpoint inhibitors is very rare. We descr...
Fingolimod (FTY) is a disease modifying therapy for relapsing remitting multiple sclerosis (RRMS) wh...