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SARA VAN DRIEST, M.D., PH.D.
M.D., PH.D.
Pediatrics Physician
NPI: 1548317357Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
MD0000045016(TN)
Research & Publications (12)
Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: septal morphological features predict the presence of myofilament mutations.
PMID 16610565·Mayo Clin Proc·2006
4-observational
Are longitudinal, natural history studies the next step in genotype-phenotype translational genomics in hypertrophic cardiomyopathy?
PMID 16256879·J Am Coll Cardiol·2005
8-other
Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy.
PMID 16087648·Eur Heart J·2005
8-other
Yield of genetic testing in hypertrophic cardiomyopathy.
PMID 15945527·Mayo Clin Proc·2005
4-observational
Molecular and functional characterization of a human frataxin mutation found in hypertrophic cardiomyopathy.
PMID 15936968·Mol Genet Metab·2005
8-other
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy.
PMID 15519027·J Am Coll Cardiol·2004
4-observational
Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy.
PMID 15358028·J Am Coll Cardiol·2004
8-other
From malignant mutations to malignant domains: the continuing search for prognostic significance in the mutant genes causing hypertrophic cardiomyopathy.
PMID 14676227·Heart·2004
8-other
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy.
PMID 12860912·Circulation·2003
8-other
Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy.
PMID 12473556·Circulation·2002
5-case
A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood.
PMID 12423715·Am J Cardiol·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 practice · 2 locations total
- Address
- 2601 TVC
NASHVILLE, TN 37232 - Phone
- (615) 322-4916
Quick Facts
- NPI
- 1548317357
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 12
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