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GAVIN RICHARD, PHARMD
PHARMD
Pharmacist
NPI: 1952275927Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
025988(LA)
Research & Publications (20)
[The reception in the school of the child with a chronic disease].
PMID 18546646·Rev Prat·2008
8-other
Comparative genomics and molecular dynamics of DNA repeats in eukaryotes.
PMID 19052325·Microbiol Mol Biol Rev·2008
6-review
Molecular evolution of minisatellites in hemiascomycetous yeasts.
PMID 16177231·Mol Biol Evol·2006
4-observational
A novel family of glucosyl 1,5-anhydro-d-fructose derivatives synthesised by transglucosylation with dextransucrase from Leuconostoc mesenteroides NRRL B-512F.
PMID 15680594·Carbohydr Res·2005
8-other
Comparative genomics of hemiascomycete yeasts: genes involved in DNA replication, repair, and recombination.
PMID 15647519·Mol Biol Evol·2005
8-other
Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.
PMID 15482471·J Invest Dermatol·2004
8-other
Contractions and expansions of CAG/CTG trinucleotide repeats occur during ectopic gene conversion in yeast, by a MUS81-independent mechanism.
PMID 12581639·J Mol Biol·2003
8-other
Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations.
PMID 12648223·J Invest Dermatol·2003
8-other
Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome.
PMID 11912510·Am J Hum Genet·2002
8-other
The spectrum of mutations in erythrokeratodermias--novel and de novo mutations in GJB3.
PMID 10798362·Hum Genet·2000
8-other
Mini- and microsatellite expansions: the recombination connection.
PMID 11265750·EMBO Rep·2000
6-review
[Scanpath of experienced and inexperienced drivers in motor sports].
PMID 19588157·Ophthalmologe·2010
4-observational
Neuronal activity influences hemodynamics in the paraoptic short posterior ciliary arteries: a comparison between healthy and glaucomatous subjects.
PMID 19578013·Invest Ophthalmol Vis Sci·2009
4-observational
Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).
PMID 19562689·Hum Mutat·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
- 1021 BEGLIS PKWY
SULPHUR, LA 70663 - Phone
- (337) 527-6575
Quick Facts
- NPI
- 1952275927
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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