Back to Search
LINDSEY POLITANO, MD
MD
Obstetrics & Gynecology Physician
NPI: 1932553112IndividualAccepts Medicare
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
01001262993(VA)
CMS Specialties
PrimaryOBSTETRICS/GYNECOLOGY
Education
OTHER
Class of 2016
Research & Publications (20)
Reliability of the North Star Ambulatory Assessment in a multicentric setting.
PMID 19553120·Neuromuscul Disord·2009
3-trial
Risk of arrhythmia in type I myotonic dystrophy: the role of clinical and genetic variables.
PMID 19237383·J Neurol Neurosurg Psychiatry·2009
8-other
Intraocular pressure and corneal biomechanical properties in patients with myotonic dystrophy.
PMID 19019447·Ophthalmology·2009
4-observational
Log-PCR: a new tool for immediate and cost-effective diagnosis of up to 85% of dystrophin gene mutations.
PMID 18403565·Clin Chem·2008
8-other
Usefulness of heart rate variability as a predictor of sudden cardiac death in muscular dystrophies.
PMID 19472920·Acta Myol·2008
6-review
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H.
PMID 17994549·Hum Mutat·2008
7-preclinical
Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients.
PMID 19472917·Acta Myol·2008
8-other
Optimal site for atrial lead implantation in myotonic dystrophy patients: the role of Bachmann's Bundle stimulation.
PMID 18950304·Pacing Clin Electrophysiol·2008
3-trial
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm.
PMID 17122938·Neurol Sci·2006
6-review
Is heart rate variability a valid parameter to predict sudden death in patients with Becker's muscular dystrophy?
PMID 17041120·Heart·2006
8-other
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes.
PMID 16141003·J Med Genet·2005
8-other
Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosis.
PMID 15954112·Hum Mutat·2005
8-other
Molecular and muscle pathology in a series of caveolinopathy patients.
PMID 15580566·Hum Mutat·2005
8-other
Research against incurability. Treatment of lethal neuromuscular diseases focused on Duchenne Muscular Dystrophy.
PMID 15938575·Acta Myol·2004
5-case
Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols.
PMID 15336688·Neuromuscul Disord·2004
3-trial
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?
PMID 15221789·Hum Mutat·2004
8-other
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia.
PMID 14981715·Am J Med Genet A·2004
6-review
Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes.
PMID 14684700·J Med Genet·2003
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
- 13801 ST FRANCIS BLVD STE 100
MIDLOTHIAN, VA 23114 - Phone
- (804) 288-4084
Quick Facts
- NPI
- 1932553112
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 10
- Publications
- 20
Are you this provider?
Claim Your Profile