Volker W. Straub

Central Parkway
Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 359 publications

Feasibility, validation and application of digital tools for remote monitoring in neuromuscular diseases: the DT4RD protocol.

Feasibility, validation and application of digital tools for remote monitoring in neuromuscular diseases: the DT4RD protocol.

Journal: BMJ open

Published: August 27, 2026

Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing.

Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

Screening cognitive and academic problems in Duchenne Muscular Dystrophy: Validity and reliability of the Kempenhaeghe Learning Questionnaire.

Screening cognitive and academic problems in Duchenne Muscular Dystrophy: Validity and reliability of the Kempenhaeghe Learning Questionnaire.

Journal: Journal of neuromuscular diseases

Published: May 30, 2026

A Validated Prognostic Score for Time to Loss of Ambulation in Patients With Duchenne Muscular Dystrophy.

A Validated Prognostic Score for Time to Loss of Ambulation in Patients With Duchenne Muscular Dystrophy.

Journal: Neurology

Published: May 26, 2026

TREAT-NMD advisory committee for therapeutics: Preclinical and clinical learnings from 15 years of TACT.

TREAT-NMD advisory committee for therapeutics: Preclinical and clinical learnings from 15 years of TACT.

Journal: Journal of neuromuscular diseases

Published: April 24, 2026

Recommendations for the use of clinical outcome assessments in rare disease drug development.

Recommendations for the use of clinical outcome assessments in rare disease drug development.

Journal: EClinicalMedicine

Published: March 05, 2026

Correspondence on 'Cardiac MRI for early detection of subclinical cardiac dysfunction in dysferlinopathy' by Thomas et al.

Correspondence on 'Cardiac MRI for early detection of subclinical cardiac dysfunction in dysferlinopathy' by Thomas et al.

Journal: Neuromuscular disorders : NMD

Published: January 09, 2026

Phenotypic characterization of dominantly inherited distal nebulin myopathy.

Phenotypic characterization of dominantly inherited distal nebulin myopathy.

Journal: Neuromuscular disorders : NMD

Published: December 23, 2025

Sensory neuronopathy secondary to gene therapy with AT845 for Pompe disease.

Sensory neuronopathy secondary to gene therapy with AT845 for Pompe disease.

Journal: Neuromuscular disorders : NMD

Published: December 19, 2025

286th ENMC international workshop: Muscle imaging: artificial intelligence, automatic segmentation and imaging data sharing in neuromuscular disease. Hoofddorp, The Netherlands, 7-9 March 2025.

286th ENMC international workshop: Muscle imaging: artificial intelligence, automatic segmentation and imaging data sharing in neuromuscular disease. Hoofddorp, The Netherlands, 7-9 March 2025.

Journal: Neuromuscular disorders : NMD

Published: December 01, 2025

Cracking the Code: Genotype-Phenotype Correlation Models in Sarcoglycanopathies.

Cracking the Code: Genotype-Phenotype Correlation Models in Sarcoglycanopathies.

Journal: Annals of clinical and translational neurology

Published: November 21, 2025

Respiratory function in Becker muscular dystrophy: a comprehensive longitudinal study.

Respiratory function in Becker muscular dystrophy: a comprehensive longitudinal study.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: October 31, 2025

Showing 1-12 of 359

Last Updated: 09/26/2026