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DAVID HALLEY, M.D.
M.D.
Orthopaedic Surgery Physician
NPI: 1649243080Individual
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
35030117H(OH)35.030117(OH)
Research & Publications (20)
Recurrent dislocation after revision total hip replacement with a large prosthetic femoral head. A case report.
PMID 15069152·J Bone Joint Surg Am·2004
5-case
Twenty- to twenty-six-year radiographic review in patients 50 years of age or younger with cemented Charnley low-friction arthroplasty.
PMID 14560415·J Arthroplasty·2003
8-other
A reliable cell-based assay for testing unclassified TSC2 gene variants.
PMID 18854862·Eur J Hum Genet·2009
8-other
Movement disorder and neuronal migration disorder due to ARFGEF2 mutation.
PMID 19384555·Neurogenetics·2009
8-other
Novel Oscillation Period of the Interlayer Exchange Coupling in Fe/Cr/Fe Due to MgO Capping.
PMID 19257313·Phys Rev Lett·2009
8-other
Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects.
PMID 19289478·J Neurol Neurosurg Psychiatry·2009
5-case
Missense mutations to the TSC1 gene cause tuberous sclerosis complex.
PMID 18830229·Eur J Hum Genet·2009
8-other
Cortical brain malformations: effect of clinical, neuroradiological, and modern genetic classification.
PMID 18332248·Arch Neurol·2008
8-other
Multiple familial trichoepithelioma and familial cylindroma: one cause!
PMID 18355210·J Eur Acad Dermatol Venereol·2008
5-case
Update of the Pompe disease mutation database with 107 sequence variants and a format for severity rating.
PMID 18425781·Hum Mutat·2008
7-preclinical
An efficient multivariate approach for estimating preference when individual observations are dependent.
PMID 18624740·J Anim Ecol·2008
7-preclinical
An incomplete trisomy 3 rescue resulting in a marker chromosome and UPD(3)--difficulties in interpretation.
PMID 18821719·Prenat Diagn·2008
5-case
Functional characterisation of the TSC1-TSC2 complex to assess multiple TSC2 variants identified in single families affected by tuberous sclerosis complex.
PMID 18302728·BMC Med Genet·2008
5-case
p.[G576S; E689K]: pathogenic combination or polymorphism in Pompe disease?
PMID 18301443·Eur J Hum Genet·2008
5-case
Overlapping neurologic and cognitive phenotypes in patients with TSC1 or TSC2 mutations.
PMID 18032745·Neurology·2008
8-other
A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting.
PMID 18625694·Gut·2008
8-other
Cognitive impairment in tuberous sclerosis complex is a multifactorial condition.
PMID 18032744·Neurology·2008
8-other
Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.
PMID 17661816·Clin Genet·2007
8-other
Evidence of a symmetry-dependent metallic barrier in fully epitaxial MgO based magnetic tunnel junctions.
PMID 17995434·Phys Rev Lett·2007
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
- 1040 DELAWARE AVENUE
MARION, OH 43302 - Phone
- (740) 383-7960
Quick Facts
- NPI
- 1649243080
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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