Nicholas Johnson, MD
Rare Disease Specialist
Virginia Commonwealth University
Richmond, Virginia
PI on 5 trials
ℹ
Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.
Report missing dataRare diseases treated or studied
Based on trial PI assignments and publication topics.
- TRAPPC11-related limb-girdle muscular dystrophy R18
- POMT2-related limb-girdle muscular dystrophy R14
- Pompe disease
- Congenital muscular dystrophy type 1B
- GMPPB-related limb-girdle muscular dystrophy R19
- Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5
- Walker-Warburg syndrome
- HNRNPDL-related limb-girdle muscular dystrophy D3
- Steinert myotonic dystrophy
- Lissencephaly
- Anoctamin-5-related limb-girdle muscular dystrophy R12
- Alpha-dystroglycan-related limb-girdle muscular dystrophy R16
- Congenital muscular dystrophy
- POMT1-related limb-girdle muscular dystrophy R11
- Calpain-3-related limb-girdle muscular dystrophy R1
- Myotonic dystrophy
- Congenital deformities of limbs
- Fukutin-related limb-girdle muscular dystrophy R13
- Late-onset Steinert myotonic dystrophy
- Plectin-related limb-girdle muscular dystrophy R17
- Progressive muscular dystrophy
- Autosomal dominant limb-girdle muscular dystrophy type 1B
- Congenital-onset Steinert myotonic dystrophy
- TNP03-related limb-girdle muscular dystrophy D2
- FKRP-related limb-girdle muscular dystrophy R9
- TOR1AIP1-related limb-girdle muscular dystrophy
- DNAJB6-related limb-girdle muscular dystrophy D1
- Genetic neurodegenerative disease
- Congenital muscular dystrophy type 1D
- Congenital myopathy