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PAMELA RICHARD, M.D.
M.D.
Pediatrics Physician
NPI: 1730183674Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
11187(LA)MD11187R(LA)
Research & Publications (20)
D-galacturonic acid catabolism in microorganisms and its biotechnological relevance.
PMID 19159926·Appl Microbiol Biotechnol·2009
6-review
Cotranscriptional recognition of human intronic box H/ACA snoRNAs occurs in a splicing-independent manner.
PMID 16537900·Mol Cell Biol·2006
8-other
Amphiphilic block copolymers promote gene delivery in vivo to pathological skeletal muscles.
PMID 16259565·Hum Gene Ther·2005
7-preclinical
Inducible production of erythropoietin using intramuscular injection of block copolymer/DNA formulation.
PMID 15468192·J Gene Med·2005
7-preclinical
A common sequence motif determines the Cajal body-specific localization of box H/ACA scaRNAs.
PMID 12912925·EMBO J·2003
8-other
Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes.
PMID 12807980·J Med Genet·2003
4-observational
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
PMID 12707239·Circulation·2003
8-other
Production of ethanol from L-arabinose by Saccharomyces cerevisiae containing a fungal L-arabinose pathway.
PMID 12702451·FEMS Yeast Res·2003
8-other
The missing link in the fungal L-arabinose catabolic pathway, identification of the L-xylulose reductase gene.
PMID 12009906·Biochemistry·2002
8-other
Cloning and expression of a fungal L-arabinitol 4-dehydrogenase gene.
PMID 11514550·J Biol Chem·2001
8-other
Impact of fluoroquinolone administration on the emergence of fluoroquinolone-resistant gram-negative bacilli from gastrointestinal flora.
PMID 11112677·Clin Infect Dis·2001
8-other
Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy.
PMID 10900182·J Mol Cell Cardiol·2000
8-other
The role of xylulokinase in Saccharomyces cerevisiae xylulose catabolism.
PMID 10981687·FEMS Microbiol Lett·2000
8-other
Visual neurophysiological dysfunction in infants exposed to hydroxychloroquine in utero.
PMID 19500079·Acta Paediatr·2009
8-other
Identification of an agrin mutation that causes congenital myasthenia and affects synapse function.
PMID 19631309·Am J Hum Genet·2009
5-case
Evolution of a pairing-induced pseudogap from the superconducting gap of (Bi,Pb)2Sr2CuO6.
PMID 19658895·Phys Rev Lett·2009
8-other
Band structure and fermi surface of an extremely overdoped iron-based superconductor KFe2As2.
PMID 19659391·Phys Rev Lett·2009
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
- 101 EAST FAIRWAY DRIVE, SUITE 302
COVINGTON, LA 70433 - Phone
- (985) 809-5800
Quick Facts
- NPI
- 1730183674
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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