Back to Search

KEVIN SPERLING, MD

MD

Nephrology Physician

NPI: 1285832543IndividualAccepts Medicare

Specialties, Licenses & Credentials

Nephrology PhysicianPrimary

Internal Medicine — Nephrology

Code: 207RN0300X

MD431835(PA)

CMS Specialties

PrimaryNEPHROLOGY

Education

UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE

Class of 2000

Research & Publications (20)

The orthopoxvirus 68-kilodalton ankyrin-like protein is essential for DNA replication and complete gene expression of modified vaccinia virus Ankara in nonpermissive human and murine cells.
PMID 19357172·J Virol·2009
7-preclinical
The highly conserved orthopoxvirus 68k ankyrin-like protein is part of a cellular SCF ubiquitin ligase complex.
PMID 18353424·Virology·2008
7-preclinical
Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.
PMID 19262743·Mol Vis·2009
5-case
A systematic proteomic study of irradiated DNA repair deficient Nbn-mice.
PMID 19412544·PLoS One·2009
7-preclinical
Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.
PMID 19309273·Genet Test Mol Biomarkers·2009
8-other
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations.
PMID 17965227·J Med Genet·2008
7-preclinical
A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.
PMID 18587493·Mol Vis·2008
8-other
High-affinity binding of southern African HIV type 1 subtype C envelope protein, gp120, to the CCR5 coreceptor.
PMID 19018669·AIDS Res Hum Retroviruses·2008
8-other
A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.
PMID 18334946·Mol Vis·2008
8-other
Extreme variation in apoptosis capacity amongst lymphoid cells of Nijmegen breakage syndrome patients.
PMID 17977616·Eur J Cell Biol·2008
8-other
Hereditary prosopagnosia: the first case series.
PMID 17710825·Cortex·2007
8-other
A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.
PMID 17893674·Mol Vis·2007
8-other
Nijmegen breakage syndrome (NBS) due to maternal isodisomy of chromosome 8.
PMID 17103455·Am J Med Genet A·2007
5-case
Polymorphisms in the DNA ligase IV gene might influence the risk of acute lymphoblastic leukemia in children.
PMID 17541392·Leukemia·2007
8-other
Cancer risk of heterozygotes with the NBN founder mutation.
PMID 18073374·J Natl Cancer Inst·2007
8-other
Molecular genetic analysis of NBS1 in German melanoma patients.
PMID 17496786·Melanoma Res·2007
8-other
A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin.
PMID 18079676·Mol Vis·2007
8-other
The granulocyte nucleus and lamin B receptor: avoiding the ovoid.
PMID 17245605·Chromosoma·2007
6-review
Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS protein.
PMID 16840438·Carcinogenesis·2007
8-other
A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.
PMID 17110920·Mol Vis·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
601 CHADDS FORD DRIVE, SUITE 100
CHADDS FORD, PA 19317

Location

Practice Location

601 CHADDS FORD DRIVE, CHADDS FORD, PA
(610) 388-0536

Quick Facts

NPI
1285832543
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
26
Publications
20

Are you this provider?

Claim Your Profile