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ABDOLAZIZ ARDALAN, M.D
M.D
Vascular Surgery Physician
NPI: 1487761607Individual
Specialties, Licenses & Credentials
Vascular Surgery PhysicianPrimary
Surgery — Vascular Surgery
Code: 2086S0129X
010267201(IN)
Research & Publications (16)
Evaluation of Golestan Province's Early Warning System for flash floods, Iran, 2006-7.
PMID 19219465·Int J Biometeorol·2009
8-other
Intrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20.
PMID 16158442·Am J Med Genet A·2005
5-case
Prevalence of primary infertility in the Islamic Republic of Iran in 2004-2005.
PMID 19443880·Asia Pac J Public Health·2009
8-other
Gender influence on hospital mortality after coronary artery bypass surgery.
PMID 18515674·Asian Cardiovasc Thorac Ann·2008
8-other
Rapid alpha-1-antitrypsin M-variant genotyping by primer-induced restriction analysis.
PMID 17471159·Diagn Mol Pathol·2007
8-other
Seroprevalence of hepatitis B in Nahavand, Islamic Republic of Iran.
PMID 17333790·East Mediterr Health J·2006
8-other
Pure direct duplication (12)(q24.1-->q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomalies.
PMID 16411218·Am J Med Genet A·2006
5-case
Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients.
PMID 16320736·Mult Scler·2005
8-other
22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.
PMID 16007629·Am J Med Genet A·2005
5-case
A new case of a severe clinical phenotype of the cat-eye syndrome.
PMID 15658620·Genet Couns·2004
5-case
Effectiveness of hepatitis B vaccination in children of chronic hepatitis B mothers.
PMID 15494813·Saudi Med J·2004
4-observational
Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens.
PMID 15333598·Hum Reprod·2004
8-other
Functional disomy of Xp including duplication of DAX1 gene with sex reversal due to t(X;Y)(p21.2;p11.3).
PMID 15216557·Am J Med Genet A·2004
8-other
Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation.
PMID 11005144·Clin Genet·2000
5-case
Prenatal detection by real-time quantitative PCR and characterization of a new CFTR deletion, 3600+15kbdel5.3kb (or CFTRdele19).
PMID 10973878·Clin Chem·2000
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
- 9737 DECATUR DR
INDIANAPOLIS, IN 46256 - Phone
- (317) 578-1133
Quick Facts
- NPI
- 1487761607
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 16
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