Fiona Norwood

Denmark Hill
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 28 publications

Access to care for adults living with spinal muscular atrophy in the UK.

Access to care for adults living with spinal muscular atrophy in the UK.

Journal: BMJ neurology open
Published: February 21, 2026

Association of British Neurologists (ABN) autoimmune myasthenia gravis management guidelines (2025 update).

Association of British Neurologists (ABN) autoimmune myasthenia gravis management guidelines (2025 update).

Journal: Practical neurology
Published: April 25, 2025

Prevalence and Geographical Distribution of Patients With Congenital Myasthenic Syndromes in the United Kingdom.

Prevalence and Geographical Distribution of Patients With Congenital Myasthenic Syndromes in the United Kingdom.

Journal: Muscle & nerve
Published: February 27, 2025

Impaired Autophagic Flux in Skeletal Muscle of Plectin-Related Epidermolysis Bullosa Simplex With Muscular Dystrophy.

Impaired Autophagic Flux in Skeletal Muscle of Plectin-Related Epidermolysis Bullosa Simplex With Muscular Dystrophy.

Journal: Journal of cachexia, sarcopenia and muscle
Published: September 16, 2024

Efgartigimod efficacy and safety in refractory myasthenia gravis: UK's first real-world experience.

Efgartigimod efficacy and safety in refractory myasthenia gravis: UK's first real-world experience.

Journal: Journal of neurology, neurosurgery, and psychiatry
Published: April 26, 2024

The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD).

The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD).

Journal: Brain : a journal of neurology
Published: February 10, 2023

Demystifying the spontaneous phenomena of motor hyperexcitability.

Demystifying the spontaneous phenomena of motor hyperexcitability.

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Published: January 28, 2021

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.

Journal: Brain : a journal of neurology
Published: June 18, 2020

Sideroblastic anemia with myopathy secondary to novel, pathogenic missense variants in the YARS2 gene.

Sideroblastic anemia with myopathy secondary to novel, pathogenic missense variants in the YARS2 gene.

Journal: Haematologica
Published: July 07, 2018

Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population.

Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population.

Journal: Journal of neurology, neurosurgery, and psychiatry
Published: February 22, 2018

Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophy.

Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophy.

Journal: Muscle & nerve
Published: October 14, 2017

Mobility shift of beta-dystroglycan as a marker of GMPPB gene-related muscular dystrophy.

Mobility shift of beta-dystroglycan as a marker of GMPPB gene-related muscular dystrophy.

Journal: Journal of neurology, neurosurgery, and psychiatry
Published: July 26, 2017
Showing 1-12 of 28

Last Updated: 09/26/2026