Louise Iterbeke
Leuven, VLG, Belgium
Last Updated: 09/26/2026
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Found 9 publications
Quantifying Disease Progression in Patients With Charcot-Marie-Tooth Neuropathy Type 1A Using Quantitative Muscle MRI and Clinical Outcomes.
Journal: Neurology
Published: August 05, 2026
Natural History of Adult-Onset Myotonic Dystrophy Type 1: Longitudinal Changes in Radiologic, Clinical, and Patient-Reported Outcomes.
Journal: Neurology
Published: July 29, 2026
Gastrointestinal manifestations are common and highly burdensome in patients with adult-onset myotonic dystrophy type 1.
Journal: Neuromuscular disorders : NMD
Published: May 28, 2026
3D Radiomic Texture Analysis of Quantitative Muscle MRI Enhances the Distinction Between Myotonic Dystrophy Type 1 and Charcot-Marie-Tooth Neuropathy Type 1A: A Proof-of-Concept Study.
Journal: European journal of neurology
Published: May 03, 2026
Two-year Risdiplam treatment in adults with spinal muscular atrophy: improvements in motor and respiratory function, quality of life and fatigue.
Journal: Neuromuscular disorders : NMD
Published: March 25, 2025
Automated Classification of Neuromuscular Diseases Using Thigh Muscle MRI With Model Interpretations.
Journal: Journal of cachexia, sarcopenia and muscle
Published: November 18, 2024
Fractures in Hereditary Neuromuscular Disorders: Frequency, Risk Factors, and Implications.
Journal: European journal of neurology
Published: November 07, 2024
Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient-reported outcome measures.
Journal: European journal of neurology
Published: December 07, 2023
Showing 1-9 of 9
Last Updated: 09/26/2026