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ERIN AKAR, MD
MD
General Practice Physician
NPI: 1528359429Individual
Specialties, Licenses & Credentials
General Practice PhysicianPrimary
General Practice
Code: 208D00000X
A133190(CA)
Research & Publications (20)
The reliability of mediastinoscopic frozen sections in deciding on oncological surgery in bronchogenic carcinoma.
PMID 18523735·Adv Ther·2008
8-other
Congenital chest wall deformities: a modified surgical technique.
PMID 17685260·Acta Chir Belg·2007
8-other
Dilemma on the treatment of haemoptysis: an analysis of 249 patients.
PMID 17685258·Acta Chir Belg·2007
8-other
First observation of homozygous hemoglobin hamadan (B 56 (D7) GLY-ARG) and beta thalassemia (-29 G>A)- hemoglobin Hamadan combination in a Turkish family.
PMID 14635211·Am J Hematol·2003
8-other
Serum amyloid A1 and tumor necrosis factor-alpha alleles in Turkish familial Mediterranean fever patients with and without amyloidosis.
PMID 12762136·Amyloid·2003
8-other
A note on mutation analysis in familial Mediterranean fever.
PMID 12632594·Pediatr Nephrol·2003
8-other
Endothelial cell protein C receptor (EPCR) gene exon III, 23 bp insertion mutation in the Turkish pediatric thrombotic patients.
PMID 12529763·Thromb Haemost·2002
8-other
657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.
PMID 12123493·Clin Genet·2002
5-case
Familial Mediterranean fever gene (MEFV) mutations in patients with rheumatic heart disease.
PMID 12010946·Heart·2002
8-other
E148Q of the MEFV gene causes amyloidosis in familial Mediterranean fever patients.
PMID 11452963·Pediatrics·2001
8-other
Plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish children with cerebral infarct and effect on factor V 1691 A mutation.
PMID 11332466·J Child Neurol·2001
8-other
The alpha2 Gene alleles of the platelet collagen receptor integrin alpha2 beta1 in Turkish children with cerebral infarct.
PMID 11323022·Thromb Res·2001
8-other
Common mutations at the homocysteine metabolism pathway and pediatric stroke.
PMID 11323021·Thromb Res·2001
8-other
Isolated recurrent pericarditis in a patient with familial Mediterranean fever.
PMID 11317655·Eur J Pediatr·2001
5-case
Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction.
PMID 11303694·Clin Cardiol·2001
8-other
Is the Ala138Gly alteration of MEFV gene important for amyloidosis?
PMID 11139244·Hum Mutat·2001
8-other
The role of prothrombotic mutations in patients with Buerger's disease.
PMID 11108900·Thromb Res·2000
8-other
Familial Mediterranean fever and systemic amyloidosis in untreated Turkish patients.
PMID 11029479·QJM·2000
8-other
Coexistence of factor V 1691 G-A and factor V 4070 A-G mutation in turkish thromboembolic patients.
PMID 10936874·Am J Hematol·2000
8-other
No association between Glu/Asp polymorphism of NOS3 gene and ischemic stroke.
PMID 10932305·Neurology·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
- 19270 SONOMA HWY 12
SONOMA, CA 95476 - Phone
- (707) 939-6070
Quick Facts
- NPI
- 1528359429
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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