Publications
176
Citations
6,676
Est. group size
—
Recurring co-author estimate
Active years
45
Publishing since 1982
Miriam Freimer's research focuses on neuromuscular disorders, especially myasthenia gravis, hereditary transthyretin amyloidosis with polyneuropathy, and inclusion body myositis. Much of the work involves clinical trials and real-world studies of drug treatments (such as zilucoplan, patisiran, tafamidis, and ravulizumab), evaluating their long-term safety, efficacy, and impact on patient symptoms and quality of life. This work is clinically oriented, often involving multicenter studies and collaborations to track patient outcomes over time.
Publication output has grown over the last decade, rising from single digits in earlier years to a peak of 21 in 2024, with a mean of about 12 publications per year over the last five years.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- An Antibody–Oligonucleotide Conjugate for Myotonic Dystrophy Type 1
New England Journal of Medicine · 2026
- Education Research: Entrustable Professional Activities for General Neurology Advanced Practice Providers
Neurology Education · 2026
- Comprehensive Care Goals in Myasthenia Gravis
Neurology Clinical Practice · 2026
- Five-Year Results With Patisiran for Hereditary Transthyretin Amyloidosis With Polyneuropathy
JAMA Neurology · 2025
- Changes in corticosteroid and non-steroidal immunosuppressive therapy with long-term zilucoplan treatment in generalized myasthenia gravis
Journal of Neurology · 2025
- Switching to subcutaneous zilucoplan from intravenous complement component 5 inhibitors in generalised myasthenia gravis: a phase IIIb, open-label study
Therapeutic Advances in Neurological Disorders · 2025
- Survival in a Contemporary, Real-World Cohort of Patients with Mixed-Phenotype Transthyretin Amyloid Cardiomyopathy Treated with Tafamidis: An Analysis from THAOS
Cardiology and Therapy · 2025
- P.107 Early and sustained response over time with zilucoplan in generalised Myasthenia Gravis: 120-week post hoc analysis of RAISE-XT
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 2025
- Switching to Subcutaneous Zilucoplan from Intravenous Complement Component 5 Inhibitors in Myasthenia Gravis: Patient Preference and Satisfaction from a Phase 3b Study (P1-11.009)
Neurology · 2025
- Effect of Zilucoplan on Myasthenia Gravis–Specific Outcome Subdomain Scores in RAISE: A Phase 3 Study (S34.004)
Neurology · 2025
- Impact of patisiran on polyneuropathy of hereditary transthyretin amyloidosis in patients with a V122I or T60A variant: a phase IV multicenter study
Annals of Medicine · 2025
- 16PComparative evaluation of respiratory assessments in inclusion body myositis from INSPIRE-IBM study
Neuromuscular Disorders · 2025
- 17PINSPIRE-IBM: an NIH-funded, two-year, multicenter, observational study in inclusion body myositis- an update and AE/SAE reporting
Neuromuscular Disorders · 2025
- 3390 Effect of zilucoplan on myasthenia gravis-specific outcome subdomain scores in RAISE: a phase 3 study
2025
- Sustained minimal symptom expression in generalized myasthenia gravis: A 120-week post hoc analyis of RAISE-XT
Journal of the Neurological Sciences · 2025
- Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature×27
- Neurology×25
- Neuromuscular Disorders×12
- The Lancet Neurology×8
- Journal of the Neurological Sciences×4
- Robert M. Pascuzzi
Medicine · Indiana University
- Song Ouyang
Medicine · The Ohio State University
- Cynthia Bodkin
Medicine · Indiana University
- Kenneth A. Kesler
Medicine · Indiana University
- Patrick J. Loehrer
Medicine · Indiana University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile