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EVE BOGER, M.D.
M.D.
Pediatrics Physician
NPI: 1235192030Individual
Specialties, Licenses & Credentials
Research & Publications (12)
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.
PMID 18279434·Clin Genet·2008
8-other
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
PMID 18181211·Hum Mutat·2008
7-preclinical
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.
PMID 17546645·Hum Mutat·2007
8-other
Arthritic pain is processed in brain areas concerned with emotions and fear.
PMID 17393440·Arthritis Rheum·2007
8-other
Paracetamol use in musculoskeletal pain: an audit of use and patient perceptions of paracetamol as an effective analgesic.
PMID 17042010·Musculoskeletal Care·2005
8-other
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.
PMID 15654330·Nat Cell Biol·2005
7-preclinical
Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle.
PMID 14610277·Proc Natl Acad Sci U S A·2003
7-preclinical
Electronic tracking board reduces ED patient length of stay at Indiana Hospital.
PMID 12556829·J Emerg Nurs·2003
8-other
DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation.
PMID 12408074·Adv Otorhinolaryngol·2002
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2201 MURPHY AVE, SUITE 201
NASHVILLE, TN 37203 - Phone
- (615) 329-3595
Quick Facts
- NPI
- 1235192030
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 12
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