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NATHAN HOWELL, MD
MD
Pediatric Orthopaedic Surgery Physician
NPI: 1497382352Individual
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
DR.0070664(CO)
Pediatric Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery — Pediatric Orthopaedic Surgery
Code: 207XP3100X
DR.0070664(CO)
Research & Publications (20)
Linking veterinary and human public-health education: collaborations at the University Of Tennessee.
PMID 18723804·J Vet Med Educ·2008
8-other
Relative rates of evolution in the coding and control regions of African mtDNAs.
PMID 17642471·Mol Biol Evol·2007
8-other
Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigree.
PMID 15599765·Hum Genet·2005
8-other
African Haplogroup L mtDNA sequences show violations of clock-like evolution.
PMID 15190127·Mol Biol Evol·2004
8-other
Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background.
PMID 12749053·Am J Med Genet A·2003
8-other
Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.
PMID 12736867·Am J Hum Genet·2003
8-other
LHON and other optic nerve atrophies: the mitochondrial connection.
PMID 12876832·Dev Ophthalmol·2003
6-review
The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates.
PMID 12571803·Am J Hum Genet·2003
8-other
Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutations.
PMID 12464729·J Neuroophthalmol·2002
5-case
Integration of problem-based learning in a veterinary medical curriculum: first-year experiences with Application-Based Learning Exercises at the University of Tennessee College of Veterinary Medicine.
PMID 12378436·J Vet Med Educ·2002
7-preclinical
mtDNA analysis of Leber hereditary optic neuropathy associated with spondyloepiphyseal dysplasia.
PMID 11343307·Am J Med Genet·2001
5-case
Longitudinal analysis of the segregation of mtDNA mutations in heteroplasmic individuals.
PMID 10620652·J Neurol Sci·2000
8-other
Persistent heteroplasmy of a mutation in the human mtDNA control region: hypermutation as an apparent consequence of simple-repeat expansion/contraction.
PMID 10762545·Am J Hum Genet·2000
8-other
Intrarenal angiotensin III infusion induces natriuresis and angiotensin type 2 receptor translocation in Wistar-Kyoto but not in spontaneously hypertensive rats.
PMID 19075092·Hypertension·2009
4-observational
Social deprivation and prognostic benefits of cardiac surgery: observational study of 44 902 patients from five hospitals over 10 years.
PMID 19342410·BMJ·2009
4-observational
Epicardial adipose tissue as a source of nuclear factor-kappaB and c-Jun N-terminal kinase mediated inflammation in patients with coronary artery disease.
PMID 18984670·J Clin Endocrinol Metab·2009
8-other
Cytotoxicity of oxidised lipids in cultured colonal human intestinal cancer cells (caco-2 cells).
PMID 18625293·Toxicol Lett·2008
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
- 13001 E 17th Pl
Aurora, CO 80045 - Phone
- (720) 777-7258
Quick Facts
- NPI
- 1497382352
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 20
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