1 enrolling by invitation. .
Follow Hereditary Motor Sensory Neuropathy: new trials by email Literature Review of Hereditary Motor Sensory Neuropathy trials Research Report on Hereditary Motor Sensory Neuropathy
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| Development and Validation of the FBIndex to Determine the Risk of Falls for Patients With Neuromuscular Disorders FBIndex - Inclusion Body Myositis, Myotonic Dystrophy | Enrolling by invitation | LMU Klinikum | 108 | 2024-09-09 | 2025-09-10 |
Amyotrophic Lateral Sclerosis (1) · Friedreich Ataxia (1) · Glycogen Storage Disease Type II (1) · Guillain-Barre Syndrome (1) · Hereditary Sensory and Motor Neuropathy (1) · Lambert-Eaton Myasthenic Syndrome (1) · Muscular Atrophy, Spinal (1) · Muscular Dystrophy, Facioscapulohumeral (1) · Myasthenia Gravis (1) · Myositis, Inclusion Body (1) · Myotonic Dystrophy (1) · Neuromuscular Diseases (1) · Polyradiculoneuropathy, Chronic Inflammatory Demyelinating (1)
Autoimmune Diseases (1) · Autoimmune Diseases of the Nervous System (1) · Brain Diseases (1) · Brain Diseases, Metabolic (1) · Brain Diseases, Metabolic, Inborn (1) · Carbohydrate Metabolism, Inborn Errors (1) · Central Nervous System Diseases (1) · Cerebellar Diseases (1) · Chronic Disease (1) · Congenital Abnormalities (1) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1) · Demyelinating Diseases (1) · Disease Attributes (1) · Genetic Diseases, Inborn (1) · Glycogen Storage Disease (1)
LMU Klinikum (1)
Germany (1)
PMID 16267188, PMID 16849828, PMID 16900450, PMID 22003934, PMID 28168524