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ERIC COTO, PHARMD
PHARMD
Pharmacist
NPI: 1578271953Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
87300(CA)
Research & Publications (20)
Clinical and analytical findings in Gitelman's syndrome associated with homozygosity for the c.1925 G>A SLC12A3 mutation.
PMID 19420906·Am J Nephrol·2009
8-other
Mutation analysis of the myocyte enhancer factor 2A gene (MEF2A) in patients with left ventricular hypertrophy/hypertrophic cardiomyopathy.
PMID 19161138·Am J Med Genet A·2009
8-other
Pharmacogenetics of calcineurin inhibitors in renal transplantation.
PMID 19667964·Transplantation·2009
8-other
[Pharmacogenetics of angiotensin system in non diabetic nephropathy].
PMID 16231503·Nefrologia·2005
4-observational
Recessive hyperekplexia due to a new mutation (R100H) in the GLRA1 gene.
PMID 16078201·Mov Disord·2005
5-case
5-Hydroxytryptamine 5-HT2A receptor and 5-hydroxytryptamine transporter polymorphisms in acute myocardial infarction.
PMID 12605580·Clin Sci (Lond)·2003
8-other
Variation at the Angiotensin-converting enzyme and endothelial nitric oxide synthase genes is associated with the risk of esophageal varices among patients with alcoholic cirrhosis.
PMID 11707686·J Cardiovasc Pharmacol·2001
4-observational
Matrix metalloproteinase 1 promoter polymorphisms and risk of myocardial infarction: a case-control study in a Spanish population.
PMID 19620856·Coron Artery Dis·2009
8-other
Mutational screening of the mortalin gene (HSPA9) in Parkinson's disease.
PMID 19657588·J Neural Transm (Vienna)·2009
8-other
Hypertrophic cardiomyopathy and athlete's heart: a tale of two entities.
PMID 18713777·Eur J Echocardiogr·2009
5-case
Differential role of serotonergic polymorphisms in alcohol and heroin dependence.
PMID 19328219·Prog Neuropsychopharmacol Biol Psychiatry·2009
8-other
Lack of association between endothelin-1 gene variants and myocardial infarction.
PMID 19672034·J Atheroscler Thromb·2009
8-other
Identification of epitopes and immunodominant regions on the MICA protein defined by alloantibodies from kidney transplant patients.
PMID 19667965·Transplantation·2009
8-other
Mutational screening of the mitochondrial transcription factors B1 and B2 (TFB1M and TFB2M) in Parkinson's disease.
PMID 18980857·Parkinsonism Relat Disord·2009
8-other
[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy].
PMID 19150014·Rev Esp Cardiol·2009
8-other
[Compound heterocygosis for intron 9 + 1 g > T and Leu850pro mutations in the SLC12A3 gene in Gitelman's syndrome].
PMID 19016647·Nefrologia·2008
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1855 COCHRAN ST
SIMI VALLEY, CA 93065 - Phone
- (805) 522-8063
Quick Facts
- NPI
- 1578271953
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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