Hospital for Special Care

Recent papers from Hospital for Special Care

1. DNL343 and Disease Progression in Amyotrophic Lateral SclerosisJAMA Network Open · 2026
2. The Impact of Sponsored Genetic Testing in 170 Consecutive Consenting Patients With Amyotrophic Lateral Sclerosis: A Single‐Site Retrospective ReviewMuscle & Nerve · 2026
3. B108-10 Validation of a Novel COPD-Specific Patient-Reported Outcome Measure for Pulmonary Rehabilitation: Preliminary Results From a Multisite StudyAmerican Journal of Respiratory and Critical Care Medicine · 2026
4. Charleston vs. Providence: are all scoliosis bending braces created equal?Journal of Pediatric Orthopaedics B · 2026
5. Impact of Areca Nut and Tobacco Dual Use on Field Cancerization: A Genomic and Cytological StudyInternational journal of oral care and research · 2025
6. Exploring Cerebrovascular Manifestations of Neuroborreliosis: A Scoping ReviewAnnals of Indian Academy of Neurology · 2026
7. Amyotrophic Lateral Sclerosis Clinical Research Site Operations: Emerging Challenges and Potential Solutions From Multiple Sites in the USMuscle & Nerve · 2025
8. Focal Neurogenic Muscle Hypertrophy and Focal Neurogenic MyositisMuscle & Nerve · 2025
9. Multicenter Expanded Access Protocol for Research Through Access to Trehalose in People With Amyotrophic Lateral SclerosisMuscle & Nerve · 2025
10. Efficacy and Safety of Zilucoplan in Amyotrophic Lateral SclerosisJAMA Network Open · 2025
11. Protein‐extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregationAnnals of Clinical and Translational Neurology · 2024
12. Multicenter expanded access program for access to investigational products for amyotrophic lateral sclerosisMuscle & Nerve · 2024
13. One-Year Recovery Among Survivors of Prolonged Severe COVID-19: A National Multicenter CohortCritical Care Medicine · 2024
14. Rare ACTN2 Frameshift Variants Resulting in Protein Extension Cause Distal Myopathy and Hypertrophic Cardiomyopathy through Protein Aggregation2024
15. Late‐onset facioscapulohumeral muscular dystrophy type 1 in previously undiagnosed families: Presenting clinical features in an often‐misdiagnosed disorderMuscle & Nerve · 2023
16. A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1AOrphanet Journal of Rare Diseases · 2021
17. Diagnostic yield of advanced genetic testing in patients with hereditary neuropathies: A retrospective single‐site studyMuscle & Nerve · 2021
18. The Toddler Autism Symptom Inventory: Use in diagnostic evaluations of toddlersAutism · 2021
19. Time spent in prior hospital stay and outcomes for ventilator patients in long-term acute care hospitalsBMC Pulmonary Medicine · 2021
20. Reldesemtiv in Patients with Spinal Muscular Atrophy: a Phase 2 Hypothesis-Generating StudyNeurotherapeutics · 2021