900 Walnut Street
Suite 200
Philadelphia, PA 19107
(215) 955-1234
Suite 200
Philadelphia, PA 19107
(215) 955-1234
Most Recent Peer-reviewed Publications
- Genetic disorders of neuromuscular ion channels
- Nomenclature of voltage-gated sodium channels
- Scholarship in the medical faculty from the university perspective: Retaining academic values
- Altered gene expression in steroid-treated denervated muscle
- Dual tandem promoter elements containing CCAC-like motifs from the tetrodotoxin-resistant voltage-sensitive Na+ channel (rSkM2) gene can independently drive muscle-specific transcription in L6 cells
- Interaction between the skeletal muscle type 1 Na + channel promoter E- box and an upstream repressor element: Release of repression by myogenin
- Ion channel mutations affecting muscle and brain
- Tandem redundant promoter elements drive rSkM2 voltage-sensitive Na+ channel expression
- Phenotype and genotype in the myotonic disorders
- Inactivation and secondary structure in the D4/S4-5 region of the SkM1 sodium channel
- Two E-boxes are the focal point of muscle-specific skeletal muscle type 1 Na+ channel gene expression
- Analysis of local structure in the D2/S1-S2 region of the rat skeletal muscle type 1 sodium channel using insertional mutagenesis
- Loss of electrical exitability in an animal model of acute quadriplegic myopathy
- Ion channel mutations and diseases of skeletal muscle
- Quality of care in academic neurology departments
- Opportunities and challenges in academic neurology: Report of the long range planning committee of the American Neurological Association
- Paramyotonia congenita mutations reveal different roles for segments S3 and S4 of domain D4 in hSkM1 sodium channel gating
- Probing sodium channel cytoplasmic domain structure: Evidence for the interaction of the rSkM1 amino and carboxyl termini
- Sodium channel mutations and disorders of excitation in human skeletal muscle
- Localization of epitopes for monoclonal antibodies directed against the adult rat skeletal muscle sodium channel (rSkM1) using polymerase chain reaction, fusion proteins, and western blotting