Chris Kneebone

A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

Nigel G. Laing, P. Anthony Akkari, S.M. Dorosz et al. · Nature Genetics · 1995 · 355 citations

Medicine, Genetics, Molecular Genetics +8

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

Elham Khalilidehkordi, Laura Clarke, Simon Arnett et al. · Frontiers in Neurology · 2020 · 47 citations · Full text

Medicine, Neurology, Neuroscience +11

The clinical profile of NMOSD in Australia and New Zealand

Wajih Bukhari, Laura Clarke, Cullen O’Gorman et al. · Journal of Neurology · 2020 · 29 citations · Full text

Medicine, Neurology, Substance Use Disorders +1

Natalizumab treatment shows low cumulative probabilities of confirmed disability worsening to EDSS milestones in the long-term setting

María Trojano, Helmut Butzkueven, Ludwig Kappos et al. · Multiple Sclerosis and Related Disorders · 2018 · 19 citations · Full text

Medicine, Neurology, Pharmacotherapy +17

The clinical relevance of <scp>MOG</scp> antibody testing in cerebrospinal fluid

Molly Reynolds, Irene Tan, Kristy Nguyen et al. · Annals of Clinical and Translational Neurology · 2024 · 16 citations · Full text

Life Sciences, Immunology, Neurology +17