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1. Oral corticosteroid dosage and tapeduration at onset in myelin oligodendrocyte glycoprotein antibody-associated disease influences time to first relapse

2. Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing alone

3. The MOG antibody non-P42 epitope is predictive of a relapsing course in MOG antibody-associated disease

5. 8 Dosing of oral corticosteroid therapy and the risk of relapse at the onset of MOGAD

6. 9 Early and late clinical features in 171 patients with LGI1-antibody encephalitis

7. 6 Spike antibody seroconversion and emerging variant cross-reactivity following COVID-19 third vaccination dose in Australian people with multiple Sclerosis

13. Diagnosis, differential diagnosis and misdiagnosis of Susac syndrome

14. Validation of a Flow Cytometry Live Cell-Based Assay to Detect Myelin Oligodendrocyte Glycoprotein Antibodies for Clinical Diagnostics

16. MRI Patterns Distinguish AQP4 Antibody Positive Neuromyelitis Optica Spectrum Disorder From Multiple Sclerosis

22. The neuro-otology of Susac syndrome

24. Relapse Patterns in NMOSD: Evidence for Earlier Occurrence of Optic Neuritis and Possible Seasonal Variation

25. The clinical profile of NMOSD in Australia and New Zealand

26. CD8+ T cell-mediated endotheliopathy is a targetable mechanism of neuro-inflammation in Susac syndrome

34. Immune-mediated conditions affecting the brain, eye and ear (BEE syndromes)

35. Forearm-predominant parainfectious myositis

37. Successful implementation of an automated electronic support system for patient safety monitoring: The alemtuzumab in multiple sclerosis safety systems (AMS3) study

39. Clinical course, therapeutic responses and outcomes in relapsing MOG antibody-associated demyelination

43. Incidence and prevalence of NMOSD in Australia and New Zealand

46. Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization

49. Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3

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