Atypical inflammatory demyelinating syndrome with central and peripheral nerve involvement

Neuroscience

• Central Nervous System 100%
• Multiple Sclerosis 100%
• Optic Neuritis 100%
• Rituximab 100%
• Intravenous Immunoglobulin 100%
• Brainstem 100%
• Ataxia 100%
• Aquaporin 4 100%
• Gene Deletion 100%
• Peripheral Nerve 100%
• Epitope 100%
• Point Mutation 100%
• Peripheral Nervous System 100%
• Midbrain Tegmentum 100%
• Polyneuropathy 100%
• Protein Sequencing 100%
• Eye Movement Disorder 100%
• Charcot-Marie-Tooth Disease 100%
• Oligoclonal Band 100%
• Myelin Oligodendrocyte Glycoprotein 100%
• Dysarthria 100%

Keyphrases

• Demyelination 100%
• Demyelinating Diseases 100%
• Central Nerve 100%
• Peripheral Nerve Involvement 100%
• Central Nervous System 20%
• Serum Antibody 20%
• Point mutation 20%
• Contrast Enhancement 20%
• Rituximab 20%
• Multiple Sclerosis 20%
• Optic Neuritis 20%
• White Matter 20%
• Duplication 20%
• Disability 20%
• Ataxia 20%
• Immunosuppressive Therapy 20%
• Aquaporin-4 (AQP4) 20%
• Immunomodulatory Therapy 20%
• New Lesion 20%
• Disease Course 20%
• Treatment Strategy 20%
• Compound Heterozygous mutation 20%
• Urinary Incontinence 20%
• Relapsing-remitting 20%
• Intravenous Immunoglobulin (IVIg) 20%
• Peripheral Nervous System 20%
• Midbrain Tegmentum 20%
• Chronic Inflammatory Demyelinating Polyneuropathy 20%
• Genome Sequence Analysis 20%
• Autoimmune Mechanism 20%
• Visual Disturbance 20%
• Eye Movement Disorders 20%
• Charcot-Marie-Tooth Disease 20%
• Oligoclonal Bands 20%
• Plasmapheresis 20%
• Variants of Uncertain Significance 20%
• Charcot-Marie-Tooth 20%
• Myelin Oligodendrocyte Glycoprotein 20%
• Parieto-occipital 20%
• Dysarthria 20%
• Sequence Deletion 20%
• Right Temporal 20%
• Tumefactive Lesion 20%
• Bilateral Sequential 20%
• Shared Epitope 20%
• McDonald Criteria 20%
• Brainstem Syndrome 20%
• SH3TC2 20%
• DYNC1H1 20%

Medicine and Dentistry

• Peripheral Nerve 100%
• Demyelination 100%
• Central Nervous System 20%
• Ataxia 20%
• Brainstem 20%
• Aquaporin 4 20%
• Optic Neuritis 20%
• Multiple Sclerosis 20%
• Epitope 20%
• Disease Course 20%
• Rituximab 20%
• Immunoglobulin 20%
• Urine Incontinence 20%
• Gene Deletion 20%
• Vision Disorder 20%
• Peripheral Nervous System 20%
• Sequence Analysis 20%
• Protein Sequencing 20%
• Heterozygosity 20%
• Tegmentum 20%
• Midbrain 20%
• Point Mutation 20%
• Chronic Inflammatory Demyelinating Polyneuropathy 20%
• Eye Movement Disorder 20%
• Plasmapheresis 20%
• Oligoclonal Band 20%
• Dysarthria 20%
• DeJerine-Sottas Disease 20%
• Myelin Oligodendrocyte Glycoprotein 20%
• McDonald Criteria 20%