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PETER HEDERA, MD
MD
Neurology Physician
NPI: 1518041615IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurological Surgery Physician
Neurological Surgery
Code: 207T00000X
MD36171(TN)
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
MD36171(TN)53689(KY)
CMS Specialties
PrimaryNEUROLOGY
Education
OTHER
Class of 1987
Research & Publications (20)
Hereditary spastic paraplegia or spinocerebellar ataxia? Not always as easy as it seems.
PMID 19453405·Eur J Neurol·2009
8-other
High-throughput mutational analysis of TOR1A in primary dystonia.
PMID 19284587·BMC Med Genet·2009
8-other
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
PMID 18718804·Parkinsonism Relat Disord·2009
8-other
Confined stimulation using dual thalamic deep brain stimulation leads rescues refractory essential tremor: report of three cases.
PMID 19641342·Stereotact Funct Neurosurg·2009
5-case
Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.
PMID 19344878·Am J Hum Genet·2009
8-other
Prevalence of unilateral tremor in autosomal dominant essential tremor.
PMID 18973247·Mov Disord·2009
8-other
Complicated autosomal recessive hereditary spastic paraplegia: a complex picture is emerging.
PMID 18413565·Neurology·2008
7-preclinical
Hereditary spastic paraplegia-associated mutations in the NIPA1 gene and its Caenorhabditis elegans homolog trigger neural degeneration in vitro and in vivo through a gain-of-function mechanism.
PMID 19091982·J Neurosci·2008
7-preclinical
Reappraisal of the role of the DRD3 gene in essential tremor.
PMID 18316228·Parkinsonism Relat Disord·2008
8-other
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
PMID 17377072·Neurology·2007
8-other
Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients.
PMID 17388992·Eur J Neurol·2007
8-other
Infantile onset of hereditary spastic paraplegia poorly predicts the genotype.
PMID 17560499·Pediatr Neurol·2007
8-other
Familial genetic predisposition, epilepsy localization and antecedent febrile seizures.
PMID 17046202·Epilepsy Res·2007
8-other
New ideas in epilepsy genetics: novel epilepsy genes, copy number alterations, and gene regulation.
PMID 17353374·Arch Neurol·2007
6-review
Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination.
PMID 17517692·Hum Mol Genet·2007
7-preclinical
Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?
PMID 16721753·Mov Disord·2006
8-other
Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy.
PMID 16839746·Epilepsy Res·2006
8-other
Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22.
PMID 17054683·Epilepsia·2006
4-observational
Systematic isolation and characterization of cDNAs encoding AAA proteins from human brain.
PMID 17425157·Bratisl Lek Listy·2006
8-other
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
- 220 ABRAHAM FLEXNER WAY FL 6
LOUISVILLE, KY 40202 - Phone
- (502) 582-7654
Quick Facts
- NPI
- 1518041615
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 39
- Publications
- 20
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