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EUGENE MCPHERSON, MD

MD

Internal Medicine Physician

NPI: 1972636108Individual

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

18836101(NY)

Research & Publications (20)

The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome.
PMID 19208384·Am J Med Genet A·2009
5-case
Ovarian failure and dilated cardiomyopathy due to a novel lamin mutation.
PMID 19283854·Am J Med Genet A·2009
5-case
A missense T (Brachyury) mutation contributes to vertebral malformations.
PMID 18466071·J Bone Miner Res·2008
8-other
Midflexion instability in revision total knee arthroplasty.
PMID 18802910·Surg Technol Int·2008
6-review
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management.
PMID 18580689·Genet Med·2008
6-review
Clinical genetics provider real-time workflow study.
PMID 18978682·Genet Med·2008
8-other
Revision total knee arthroplasty for excessive ligamentotaxis.
PMID 18078894·J Arthroplasty·2007
5-case
Renal anomalies in families of individuals with congenital solitary kidney.
PMID 17505207·Genet Med·2007
8-other
Incision stretching in primary TKA: what is the real length of our approach?
PMID 17539214·Orthopedics·2007
8-other
Reduction in early dislocation rate with large-diameter femoral heads in primary total hip arthroplasty.
PMID 17823033·J Arthroplasty·2007
8-other
Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations.
PMID 17888180·Scoliosis·2007
8-other
Exercise training improves cardiovascular and autonomic profiles in HIV.
PMID 18049834·Clin Auton Res·2007
8-other
Acute health events in adult patients with genetic disorders: the Marshfield Epidemiologic Study Area.
PMID 16912579·Genet Med·2006
8-other
Patellar tracking in primary total knee arthroplasty.
PMID 16958479·Instr Course Lect·2006
6-review
Robinow syndrome with variable neurologic features.
PMID 16418601·Genet Med·2006
5-case
Variable outcomes in mosaic trisomy 16: five case reports and literature analysis.
PMID 16557642·Prenat Diagn·2006
5-case
Evaluation of SLC35A3 as a candidate gene for human vertebral malformations.
PMID 16691598·Am J Med Genet A·2006
8-other
Genetic diagnosis and testing in clinical practice.
PMID 16809405·Clin Med Res·2006
6-review
Prenatal diagnosis of episodic tachypnea in an infant with OFD VI.
PMID 16906567·Am J Med Genet A·2006
5-case
DLL3 as a candidate gene for vertebral malformations.
PMID 17041936·Am J Med Genet A·2006
5-case

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
1752 PARK AVE
NEW YORK, NY 10035

Location

Practice Location

1752 PARK AVE, NEW YORK, NY
(646) 686-0000

Quick Facts

NPI
1972636108
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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