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PAUL RICHARD, DO
DO
Family Medicine Physician
NPI: 1952810558IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
DO.2152(AL)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
ALABAMA COLLEGE OF OSTEOPATHIC MEDICINE
Class of 2017
Research & Publications (20)
D-galacturonic acid catabolism in microorganisms and its biotechnological relevance.
PMID 19159926·Appl Microbiol Biotechnol·2009
6-review
Angle-resolved photoemission spectroscopy of the Fe-Based Ba0.6K0.4Fe2As2 high temperature superconductor: evidence for an orbital selective electron-mode coupling.
PMID 19257465·Phys Rev Lett·2009
8-other
A synonymous CHRNE mutation responsible for an aberrant splicing leading to congenital myasthenic syndrome.
PMID 17363247·Neuromuscul Disord·2007
5-case
Inducible production of erythropoietin using intramuscular injection of block copolymer/DNA formulation.
PMID 15468192·J Gene Med·2005
7-preclinical
Amphiphilic block copolymers promote gene delivery in vivo to pathological skeletal muscles.
PMID 16259565·Hum Gene Ther·2005
7-preclinical
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
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
Identification of an agrin mutation that causes congenital myasthenia and affects synapse function.
PMID 19631309·Am J Hum Genet·2009
5-case
DNA/amphiphilic block copolymer nanospheres promote low-dose DNA vaccination.
PMID 19417740·Mol Ther·2009
7-preclinical
A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy.
PMID 19429631·Eur Heart J·2009
4-observational
Visual neurophysiological dysfunction in infants exposed to hydroxychloroquine in utero.
PMID 19500079·Acta Paediatr·2009
8-other
Band structure and fermi surface of an extremely overdoped iron-based superconductor KFe2As2.
PMID 19659391·Phys Rev Lett·2009
8-other
Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia.
PMID 19364651·Neuromuscul Disord·2009
8-other
Evolution of a pairing-induced pseudogap from the superconducting gap of (Bi,Pb)2Sr2CuO6.
PMID 19658895·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
- 4371 NARROW LANE RD STE 100
MONTGOMERY, AL 36116 - Phone
- (334) 613-3680
Quick Facts
- NPI
- 1952810558
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 9
- Publications
- 20
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