Dr. Stephen J. Kolb MD, PHD
Neurologist | Neurology
1654 Upham Dr 445 Means Hall Columbus OH, 43210Rating
1/5
About
I approach patient care the way I would expect my physician to approach me - with competence, honesty and a collaborative style. I am a physician/scientist. I care for patients who suffer from Lou G ... ...
Board Certification
Psychiatry and NeurologyAmerican Board of Psychiatry and NeurologyABPN
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Light scattering and transmission electron microscopy studies reveal a mechanism for calcium/calmodulin-dependent protein kinase II self-association.
- The survival of motor neurons protein determines the capacity for snRNP assembly: biochemical deficiency in spinal muscular atrophy.
- Channel permeant cations compete selectively with noncompetitive inhibitors of the nicotinic acetylcholine receptor.
- Molecular functions of the SMN complex.
- RNA processing defects associated with diseases of the motor neuron.
- Spliceosomal small nuclear ribonucleoprotein biogenesis defects and motor neuron selectivity in spinal muscular atrophy.
- Mutant HSPB1 overexpression in neurons is sufficient to cause age-related motor neuronopathy in mice.
- Direct conversion of patient fibroblasts demonstrates non-cell autonomous toxicity of astrocytes to motor neurons in familial and sporadic ALS.
- Safety, pharmacokinetic, and functional effects of the nogo-a monoclonal antibody in amyotrophic lateral sclerosis: a randomized, first-in-human clinical trial.
- NeuroNEXT SMA biomarkers study.
- A large animal model of spinal muscular atrophy and correction of phenotype.
- Electrophysiological Motor Unit Number Estimation (MUNE) Measuring Compound Muscle Action Potential (CMAP) in Mouse Hindlimb Muscles.
- Genetic testing and genetic counseling for amyotrophic lateral sclerosis: an update for clinicians.
- Spinal Muscular Atrophy Biomarker Measurements from Blood Samples in a Clinical Trial of Valproic Acid in Ambulatory Adults.
- Variable phenotypic expression and onset in MYH14 distal hereditary motor neuropathy phenotype in a large, multigenerational North American family.
Clinical Trials
Fellowships
- Research: University of Pennsylvania Hospital 2002
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