Search Results - "Roxburgh, R."

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Sanction of international law.

Authors: Roxburgh, R. F.

Source: American Journal of International Law; January 1920, Vol. 14, p26-37, 12p

Peripheral nerves are pathologically small in cerebellar ataxia neuropathy vestibular areflexia syndrome: a controlled ultrasound study.

Authors: Pelosi, L. Mulroy, E. Leadbetter, R. et al.

Source: European Journal of Neurology. Apr2018, Vol. 25 Issue 4, p659-665. 7p. 1 Diagram, 2 Charts, 1 Graph.

Subjects: Cerebellar ataxia, Neuropathy, Nerves, Ultrasonic imaging, Vestibular stimulation

Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis

Authors: Hensiek, A.E. Roxburgh, R. Smilie, B. et al.

Source: Journal of Neuroimmunology. Oct2003, Vol. 143 Issue 1/2, p25. 6p.

Osteopontin gene and clinical severity of multiple sclerosis.

Authors: Hensiek, A. E. Roxburgh, R. Meranian, M. et al.

Source: Journal of Neurology. Aug2003, Vol. 250 Issue 8, p943-947. 5p.

P.212 TREAT-NMD Myotonic dystrophy (DM) Global Registry Network: An update in 2022.

Authors: Bennett, N. Roxburgh, R. Porter, B. et al.

Source: Neuromuscular Disorders. 2022 Supplement 1, Vol. 32, pS132-S132. 1p.

Spontaneous low-pressure headache complicating bagpiping.

Authors: Patrick A McAuley D Roxburgh R

Source: Headache: The Journal of Head & Face Pain. Apr2007, Vol. 47 Issue 4, p611-613. 3p.

Theme 2 Genetics and Genomics.

Authors: Mrkela, M. Rodrigues, M. Naidoo, S. et al.

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 2024 Suppl 1, Vol. 25, p105-121. 17p.

Relationships Between Nerve Ultrasound Findings and Clinical, Genetic, Laboratory and Electrophysiological Findings in Patients With Chronic Idiopathic Axonal Polyneuropathy.

Authors: Pelosi, L. Garvey, A. Melville, I. Z. et al.

Source: Muscle & Nerve. Feb2026, Vol. 73 Issue 2, p340-345. 6p.

REGISTRIES AND CARE OF NEUROMUSCULAR DISORDERS: P.289Patients experience of diagnosis of a genetic muscle disorder.

Authors: Rodrigues, M. Roxburgh, R. O'Grady, G. et al.

Source: Neuromuscular Disorders. Oct2018:Supplement 2, Vol. 28, pS118-S118. 1p.

P.407 - Prevalence of genetic muscle disorders (MD-Prev): A national, population-based study.

Authors: Theadom, A. Roxburgh, R. Rodrigues, M. et al.

Source: Neuromuscular Disorders. Oct2016 Supplement 2, Vol. 26, pS206-S206. 1p.

P4.63 The New Zealand neuromuscular disease registry

Authors: Rodrigues, M.J. Roxburgh, R. Kidd, A. et al.

Source: Neuromuscular Disorders. Oct2011, Vol. 21 Issue 9/10, p723-723. 1p.

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Phase relationships and sulphide capacities in slags from the lime-magnesia-titania-silica system

Authors: Roxburgh, R. J.

URL: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.880359

Basic derivatives of fluorene and anthracene, and isomerisation reactions with hydrogen fluoride

Authors: Aitken, Roxburgh R.

URL: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.803128

The diagnostic importance of glycosuria in lead poisoning in childhood.

Authors: ROXBURGH, RONALD C. HAAS, LEONARD ROXBURGH, R C et al.

Source: Archives of Disease in Childhood. Feb1959, Vol. 34 Issue 173, p70-73. 4p.

357PLong-term vatiquinone treatment slows Friedreich's ataxia disease progression relative to FACOMS natural history.

Authors: Vagabov, A. Cherry, J. Duqette, A. et al.

Source: Neuromuscular Disorders. 2025 Supplement, Vol. 53, pN.PAG-N.PAG. 1p.

546PClinical research facilitated by the New Zealand neurogenetic registry & biobank.

Authors: Rodrigues, M. Buchanan, C. O'Grady, G. et al.

Source: Neuromuscular Disorders. 2025 Supplement, Vol. 53, pN.PAG-N.PAG. 1p.

391PA prospective longitudinal observational study in myotonic dystrophy type 1 (DM1): from clinical outcomes and endpoints to clinical trial design.

Authors: Sansone, V. Aggradi, C. Ferrari Lizio, A. et al.

Source: Neuromuscular Disorders. 2025 Supplement, Vol. 53, pN.PAG-N.PAG. 1p.

380PDYNE-101 targets the underlying cause of DM1 to enable multi-system functional improvement in the ACHIEVE trial.

Authors: Kerr, D. Sansone, V. Bassez, G. et al.

Source: Neuromuscular Disorders. 2025 Supplement, Vol. 53, pN.PAG-N.PAG. 1p.