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ALBERT SHU, MD
MD
Internal Medicine Physician
NPI: 1639602071IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
S03-009-797(KY)
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
MD210002623(DC)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
UNIVERSITY OF LOUISVILLE SCHOOL OF MEDICINE
Class of 2019
Research & Publications (20)
Adherence to osteoporosis medications after patient and physician brief education: post hoc analysis of a randomized controlled trial.
PMID 19589009·Am J Manag Care·2009
2-rct
Systematic screening for polymorphisms within the UGT1A6 gene in three Chinese populations and function prediction through structural modeling.
PMID 19450126·Pharmacogenomics·2009
8-other
Pharmacokinetics and brain penetration of casopitant, a potent and selective neurokinin-1 receptor antagonist, in the ferret.
PMID 18556439·Drug Metab Dispos·2008
7-preclinical
Evidence of DNA transfer through F-pilus channels during Escherichia coli conjugation.
PMID 18522439·Langmuir·2008
8-other
[Genetic analysis of a Chinese pedigree with split hand and foot malformation].
PMID 18067070·Zhonghua Yi Xue Yi Chuan Xue Za Zhi·2007
8-other
Differences in CYP3A41G genotype distribution and haplotypes of CYP3A4, CYP3A5 and CYP3A7 in 3 Chinese populations.
PMID 17582393·Clin Chim Acta·2007
8-other
Screening for SNPs and haplotypes in the CYP3A7 gene in Chinese populations.
PMID 17559345·Pharmacogenomics·2007
4-observational
Chimeric protein for selective cell attachment onto cellulosic substrates.
PMID 17430973·Protein Eng Des Sel·2007
7-preclinical
Systematic screening for polymorphisms in the CYP3A4 gene in the Chinese population.
PMID 16981844·Pharmacogenomics·2006
8-other
A novel mutation of PAX3 in a Chinese family with Waardenburg syndrome.
PMID 16971891·Mol Vis·2006
8-other
[Mutation analysis of 12S rRNA and tRNA-Ser(UCN) genes in a large Chinese family with maternally inherited nonsyndromic hearing loss by intermarriage].
PMID 16767669·Zhonghua Yi Xue Yi Chuan Xue Za Zhi·2006
8-other
[A family with nonsyndromic hearing impairment caused by intermarry].
PMID 16120576·Yi Chuan·2005
8-other
[Mutation detection of COL1A1 gene in a pedigree with osteogenesis imperfecta].
PMID 15931785·Yi Chuan Xue Bao·2005
8-other
Improved methods for 1H-3H heteronuclear shift correlation.
PMID 15593350·Magn Reson Chem·2005
8-other
Inhibition of wild-type and mutant human immunodeficiency virus type 1 proteases by GW0385 and other arylsulfonamides.
PMID 15533054·Biochemistry·2004
4-observational
A novel insertion mutation in the FOXL2 gene is detected in a big Chinese family with blepharophimosis-ptosis-epicanthus inversus.
PMID 15450400·Mutat Res·2004
8-other
[Genetic analysis of a Chinese pedigree with congenital synpolydactyly].
PMID 14669516·Yi Chuan Xue Bao·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
- 2233 WISCONSIN AVE NW STE 300
WASHINGTON, DC 20007 - Phone
- (202) 714-1250
Quick Facts
- NPI
- 1639602071
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 7
- Publications
- 20
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