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SHADAIN AKHAVAN MD
MD
Obstetrics & Gynecology Physician
NPI: 1851970024IndividualAccepts Medicare
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
116035862(VA)MD224356(OR)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Education
EASTERN VIRGINIA MEDICAL SCHOOL
Class of 2021
Research & Publications (20)
Clinical outcome of a fibermetal taper stem: minimum 5-year followup.
PMID 17767076·Clin Orthop Relat Res·2007
8-other
Health in relation to unemployment and sick leave among immigrants in Sweden from a gender perspective.
PMID 15269514·J Immigr Health·2004
8-other
Phenotypic and genetic analysis of a compound heterozygote for dys- and hypoprothrombinaemia.
PMID 12492590·Br J Haematol·2003
5-case
Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype.
PMID 12149217·Blood·2002
5-case
Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiency.
PMID 11154146·Thromb Haemost·2000
8-other
Natural variability of NS3 protease in patients infected with genotype 4 hepatitis C virus (HCV): implications for antiviral treatment using specifically targeted antiviral therapy for HCV.
PMID 19604114·J Infect Dis·2009
8-other
Impact of hepatitis B virus genotypes and surface antigen variants on the performance of HBV real time PCR quantification.
PMID 19406163·J Virol Methods·2009
4-observational
Complications of anterior cruciate ligament reconstruction.
PMID 19385548·Instr Course Lect·2009
8-other
Steroids and risk factors for airway compromise in multilevel cervical corpectomy patients: a prospective, randomized, double-blind study.
PMID 19148042·Spine (Phila Pa 1976)·2009
2-rct
A two adenine insertion polymorphism in the 3' untranslated region of factor VII gene is associated with peripheral arterial disease but not with venous thrombosis. Results of case-control studies.
PMID 17938795·Thromb Haemost·2007
7-preclinical
Recurrence of a Phe31Ser mutation in the Gla domain of blood coagulation factor X, in unrelated Algerian families: a founder effect?
PMID 17391309·Eur J Haematol·2007
7-preclinical
Clinical and histologic results related to a low-modulus composite total hip replacement stem.
PMID 16757765·J Bone Joint Surg Am·2006
8-other
The natural mutation by deletion of Lys9 in the thrombin A-chain affects the pKa value of catalytic residues, the overall enzyme's stability and conformational transitions linked to Na+ binding.
PMID 16367756·FEBS J·2006
4-observational
A critical role for Gly25 in the B chain of human thrombin.
PMID 15634277·J Thromb Haemost·2005
7-preclinical
A natural prothrombin mutant reveals an unexpected influence of A-chain structure on the activity of human alpha-thrombin.
PMID 14722067·J Biol Chem·2004
7-preclinical
The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiency.
PMID 15566361·Br J Haematol·2004
5-case
Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency.
PMID 12028042·Br J Haematol·2002
8-other
Two naturally occurring mutations on FVII gene (S363I-W364C) altering intrinsic catalytic activity.
PMID 12428089·Thromb Haemost·2002
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via INOVA FAIRFAX HOSPITAL · 3 locations total
- Address
- 3300 GALLOWS RD
FALLS CHURCH, VA 22042 - Phone
- (703) 776-2745
Quick Facts
- NPI
- 1851970024
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 3
- Years in Practice
- 5
- Publications
- 20
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