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MILAD SANATI, PHARMD
PHARMD
Pharmacist
NPI: 1720690001Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
051.301674(IL)051301674(IL)
Research & Publications (20)
IgG subclasses pattern and high-avidity antibody to the C-terminal region of merozoite surface protein 1 of Plasmodium vivax in an unstable hypoendemic region in Iran.
PMID 19481997·Acta Trop·2009
7-preclinical
Mitochondrial mutation in Iranian patients with multiple sclerosis, correlation between haplogroups H, A and clinical manifestations.
PMID 19009343·Cell Mol Neurobiol·2009
8-other
Alternative splicing in the synaptic protein interaction site of rat Ca(v)2.2 (alpha (1B)) calcium channels: changes induced by chronic inflammatory pain.
PMID 19125229·J Mol Neurosci·2009
7-preclinical
The immunobiology of CD154-CD40-TRAF interactions in atherosclerosis.
PMID 19616449·Semin Immunol·2009
6-review
Plasmodium falciparum: sequence analysis of the gene encoding the C-terminus region of the merozoite surface protein-1, a potential malaria vaccine antigen, in Iranian clinical isolates.
PMID 18053992·Exp Parasitol·2008
7-preclinical
The autoimmune diseases manifested by production of autoantibodies: the autoantigens identified by random peptide library.
PMID 18780947·Iran J Allergy Asthma Immunol·2008
6-review
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11.
PMID 18616530·Clin Genet·2008
8-other
A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.
PMID 18394579·Am J Hum Genet·2008
7-preclinical
The influence of uric acid treatments on liver glutathione system prevent oxidative damages in experimental autoimmune encephalomyelitis mice.
PMID 18501514·Neurosci Lett·2008
7-preclinical
Variation of DAT1 VNTR alleles and genotypes among old ethnic groups in Mesopotamia to the Oxus region.
PMID 18505046·Hum Biol·2008
8-other
A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.
PMID 18022253·Int J Pediatr Otorhinolaryngol·2008
8-other
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
PMID 17591938·J Mol Diagn·2007
4-observational
Relationship between the clinical scoring and demyelination in central nervous system with total antioxidant capacity of plasma during experimental autoimmune encephalomyelitis development in mice.
PMID 17157437·Neurosci Lett·2007
7-preclinical
Gene dosage is not responsible for the upregulation of MRP1 gene expression in adult leukemia patients.
PMID 17350479·Arch Med Res·2007
8-other
A comprehensive study on the major mutations in glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in the coastal provinces of Caspian Sea in the north of Iran.
PMID 17499234·Clin Biochem·2007
8-other
Use of D11S2179 and D11S1343 as markers for prenatal diagnosis of ataxia telangiectasia in Iranian patients.
PMID 17845903·Arch Med Res·2007
8-other
Growth kinetics and Pho84 phosphate transporter activity of Saccharomyces cerevisiae under phosphate-limited conditions.
PMID 17109161·J Ind Microbiol Biotechnol·2007
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
- 900 DODGE AVE
EVANSTON, IL 60202 - Phone
- (847) 475-7287
Quick Facts
- NPI
- 1720690001
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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