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LAMEH FANANAPAZIR, M.D.
M.D.
Cardiovascular Disease Physician
NPI: 1568409415Individual
Specialties, Licenses & Credentials
Specialist
Specialist
Code: 174400000X
D0039832(MD)
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
D0039832(MD)
Clinical Cardiac Electrophysiology Physician
Internal Medicine — Clinical Cardiac Electrophysiology
Code: 207RC0001X
D0039832(MD)
Research & Publications (20)
Ventilatory efficiency and resting hemodynamics in hypertrophic cardiomyopathy.
PMID 18408621·Med Sci Sports Exerc·2008
8-other
Modification of human hearing loss by plasma-membrane calcium pump PMCA2.
PMID 15829536·N Engl J Med·2005
5-case
Left atrial volumetric remodeling is predictive of functional capacity in nonobstructive hypertrophic cardiomyopathy.
PMID 15990760·Am Heart J·2005
8-other
Molecular and phenotypic effects of heterozygous, homozygous, and compound heterozygote myosin heavy-chain mutations.
PMID 15528230·Am J Physiol Heart Circ Physiol·2005
8-other
Myocardial bridging in adult and pediatric patients with hypertrophic cardiomyopathy is not associated with poor outcome.
PMID 15028383·J Am Coll Cardiol·2004
8-other
Cerebellar ataxia, seizures, premature death, and cardiac abnormalities in mice with targeted disruption of the Cacna2d2 gene.
PMID 15331424·Am J Pathol·2004
4-observational
Chorein detection for the diagnosis of chorea-acanthocytosis.
PMID 15293285·Ann Neurol·2004
4-observational
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6).
PMID 15060111·J Med Genet·2004
8-other
Genomic organization, alternative splicing, and expression of human and mouse N-RAP, a nebulin-related LIM protein of striated muscle.
PMID 12789664·Cell Motil Cytoskeleton·2003
7-preclinical
Assessment of regional systolic and diastolic dysfunction in familial hypertrophic cardiomyopathy using MR tagging.
PMID 12939774·Magn Reson Med·2003
8-other
Efficacy of implantable cardioverter defibrillator therapy for primary and secondary prevention of sudden cardiac death in hypertrophic cardiomyopathy.
PMID 12930505·Pacing Clin Electrophysiol·2003
8-other
Utility of genetic screening in hypertrophic cardiomyopathy: prevalence and significance of novel and double (homozygous and heterozygous) beta-myosin mutations.
PMID 12820698·Genet Test·2003
8-other
Mutations of MYO6 are associated with recessive deafness, DFNB37.
PMID 12687499·Am J Hum Genet·2003
8-other
Systolic compression of epicardial coronary and intramural arteries in children with hypertrophic cardiomyopathy.
PMID 12484613·Tex Heart Inst J·2002
8-other
Microarray gene expression profiles in dilated and hypertrophic cardiomyopathic end-stage heart failure.
PMID 12118103·Physiol Genomics·2002
4-observational
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis.
PMID 12404112·Eur J Hum Genet·2002
8-other
Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.
PMID 11407343·N Engl J Med·2001
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
- 12502 WILLOWBROOK ROAD, SUITE 420
CUMBERLAND, MD 21502 - Phone
- (301) 777-1997
Quick Facts
- NPI
- 1568409415
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
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