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NIKA HOWELL, M.D.
M.D.
Pediatrics Physician
NPI: 1396037750Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
A 132660(CA)
Hospitalist Physician
Hospitalist
Code: 208M00000X
A 132660(CA)
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
Mild renal dysfunction predicts in-hospital mortality and post-discharge survival following cardiac surgery.
PMID 18502144·Eur J Cardiothorac Surg·2008
8-other
Concentrations of polychlorinated biphenyls (PCBs) in water, sediment, and aquatic biota in the Houston Ship Channel, Texas.
PMID 17850847·Chemosphere·2008
7-preclinical
Relative rates of evolution in the coding and control regions of African mtDNAs.
PMID 17642471·Mol Biol Evol·2007
8-other
Patient-prosthesis mismatch does not affect survival following aortic valve replacement.
PMID 16723251·Eur J Cardiothorac Surg·2006
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
LHON and other optic nerve atrophies: the mitochondrial connection.
PMID 12876832·Dev Ophthalmol·2003
6-review
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
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
mtDNA analysis of Leber hereditary optic neuropathy associated with spondyloepiphyseal dysplasia.
PMID 11343307·Am J Med Genet·2001
5-case
Elucidation of protein-lipid interactions in a lysozyme-corn oil system by Fourier transform Raman spectroscopy.
PMID 11312891·J Agric Food Chem·2001
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
Longitudinal analysis of the segregation of mtDNA mutations in heteroplasmic individuals.
PMID 10620652·J Neurol Sci·2000
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
- 9300 VALLEY CHILDRENS PL
MADERA, CA 93636 - Phone
- (559) 353-5068
Quick Facts
- NPI
- 1396037750
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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