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KATHLEEN TALBOT, MD
MD
Family Medicine Physician
NPI: 1841258274Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
35.053141(OH)
Research & Publications (20)
Reduction of elevated IGF-1 levels in coincident amyotrophic lateral sclerosis and acromegaly.
PMID 19634028·Amyotroph Lateral Scler·2010
5-case
Neurobehavioral abnormalities in the dysbindin-1 mutant, sandy, on a C57BL/6J genetic background.
PMID 19220483·Genes Brain Behav·2009
7-preclinical
Investigation of white matter pathology in ALS and PLS using tract-based spatial statistics.
PMID 18172851·Hum Brain Mapp·2009
8-other
Differential contributions of Glu96, Asp102 and Asp111 to coagulation factor V/Va metal ion binding and subunit stability.
PMID 19522703·Biochem J·2009
4-observational
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
PMID 19193627·Hum Mol Genet·2009
8-other
Progressive unsteadiness in a 68-year-old man with longstanding abdominal pain and altered bowel habit.
PMID 19608770·Pract Neurol·2009
5-case
Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model.
PMID 19332122·Neurobiol Dis·2009
7-preclinical
Dysbindin-1 in dorsolateral prefrontal cortex of schizophrenia cases is reduced in an isoform-specific manner unrelated to dysbindin-1 mRNA expression.
PMID 19617633·Hum Mol Genet·2009
8-other
TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.
PMID 18957104·BMC Neurosci·2008
7-preclinical
Caspase-3 is enriched in postsynaptic densities and increased in Alzheimer's disease.
PMID 18818379·Am J Pathol·2008
8-other
Low sociability is associated with reduced size of the corpus callosum in the BALB/cJ inbred mouse strain.
PMID 18662677·Brain Res·2008
7-preclinical
Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS.
PMID 18282652·Prog Neurobiol·2008
6-review
Asymmetrical late onset motor neuropathy associated with a novel mutation in the small heat shock protein HSPB1 (HSP27).
PMID 18344398·J Neurol Neurosurg Psychiatry·2008
5-case
Candidate screening of the bovine and feline spinal muscular atrophy genes reveals no evidence for involvement in human motor neuron disorders.
PMID 18395445·Neuromuscul Disord·2008
7-preclinical
Activation of mutant protein kinase Cgamma leads to aberrant sequestration and impairment of its cellular function.
PMID 18503760·Biochem Biophys Res Commun·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 1500 E 17TH AVE
COLUMBUS, OH 43219 - Phone
- (614) 645-2700
Quick Facts
- NPI
- 1841258274
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
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