Maggie C. Walter

Central Parkway
Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 136 publications

Functional disease progression in children with inherited peripheral neuropathies: A prospective cohort study.

Functional disease progression in children with inherited peripheral neuropathies: A prospective cohort study.

Journal: Journal of neuromuscular diseases

Published: July 03, 2026

Identification of prognostic biomarkers in a large cohort of patients with LGMD R2.

Identification of prognostic biomarkers in a large cohort of patients with LGMD R2.

Journal: Journal of neurology

Published: March 10, 2026

Psychological symptoms in individuals with Spinal Muscular Atrophy (SMA) and their caregivers - results from a nation-wide study in Germany.

Psychological symptoms in individuals with Spinal Muscular Atrophy (SMA) and their caregivers - results from a nation-wide study in Germany.

Journal: Orphanet journal of rare diseases

Published: November 11, 2025

Expert Consensus on Genetic Diagnostic Approaches for Patients With Limb-Girdle Muscular Dystrophy.

Expert Consensus on Genetic Diagnostic Approaches for Patients With Limb-Girdle Muscular Dystrophy.

Journal: Neurology

Published: October 28, 2025

State of the art: Pregnancy in spinal muscular atrophy in the treatment era.

State of the art: Pregnancy in spinal muscular atrophy in the treatment era.

Journal: Journal of neuromuscular diseases

Published: September 12, 2025

Phenotypic intrafamilial variability of 5q-associated spinal muscular atrophy: A systematic multicentre sibling study.

Phenotypic intrafamilial variability of 5q-associated spinal muscular atrophy: A systematic multicentre sibling study.

Journal: Journal of neuromuscular diseases

Published: September 12, 2025

Treatment evolution in spinal muscular atrophy: insights from the SMArtCARE registry.

Treatment evolution in spinal muscular atrophy: insights from the SMArtCARE registry.

Journal: Brain : a journal of neurology

Published: September 01, 2025

Whole-Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies.

Whole-Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies.

Journal: Annals of clinical and translational neurology

Published: August 22, 2025

Measuring health-related quality of life in spinal muscular atrophy - Lessons learned from a Nationwide registry study in Germany.

Measuring health-related quality of life in spinal muscular atrophy - Lessons learned from a Nationwide registry study in Germany.

Journal: Journal of the neurological sciences

Published: August 04, 2025

Reduced Muscle Force in Dystrophic DMDΔ52 Pigs Is Incompletely Restored by Systemic Transcript Reframing (DMDΔ51-52).

Reduced Muscle Force in Dystrophic DMDΔ52 Pigs Is Incompletely Restored by Systemic Transcript Reframing (DMDΔ51-52).

Journal: Journal of cachexia, sarcopenia and muscle

Published: February 26, 2025

Disease spectrum and long-term prognosis of patients with BAG3-associated neuromuscular diseases in Europe.

Disease spectrum and long-term prognosis of patients with BAG3-associated neuromuscular diseases in Europe.

Journal: Brain : a journal of neurology

Published: January 27, 2025

Agreement Between Child Self- and Parent Proxy-Reports of Health-Related Quality of Life in Spinal Muscular Atrophy: Preliminary Insights from a Nationwide Patient Registry in Germany.

Agreement Between Child Self- and Parent Proxy-Reports of Health-Related Quality of Life in Spinal Muscular Atrophy: Preliminary Insights from a Nationwide Patient Registry in Germany.

Journal: Patient related outcome measures

Published: January 24, 2025

Showing 1-12 of 136

Last Updated: 09/26/2026