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BENJAMIN ENG, M.D.
M.D.
Family Medicine Physician
NPI: 1992779144Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
0101032402(VA)
Research & Publications (20)
Characterization of a long-term rat mTAL cell line.
PMID 17670898·Am J Physiol Renal Physiol·2007
7-preclinical
Impact of a public antiretroviral program on TB/HIV mortality: Banteay Meanchey, Cambodia.
PMID 19323039·Southeast Asian J Trop Med Public Health·2009
8-other
Association between distance to HIV testing site and uptake of HIV testing for tuberculosis patients in Cambodia.
PMID 19146752·Int J Tuberc Lung Dis·2009
8-other
Novel 27.9 kb alpha(0)-thalassemia deletion in a Filipino woman.
PMID 19195033·Am J Hematol·2009
5-case
Characterisation of the British alpha 0-thalassaemia deletion: evidence of a founder effect in Newfoundland, Canada.
PMID 19622095·Br J Haematol·2009
8-other
Hb North York [beta 117(G19)His-->Asp]: a new beta chain hemoglobin variant.
PMID 19205973·Hemoglobin·2009
5-case
Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG).
PMID 19205977·Hemoglobin·2009
5-case
Systematic review on quality control for drug management programs: is quality reported in the literature?
PMID 19243591·BMC Health Serv Res·2009
1-meta
Three new beta-thalassemia mutations with varying degrees of severity.
PMID 19657836·Hemoglobin·2009
5-case
Systematic analysis of outcomes evaluations applied to drug management programs.
PMID 18991480·Am J Manag Care·2008
1-meta
Frameshift mutation in the alpha2-globin gene causing alpha+ -thalassemia: codon 49 (-GC).
PMID 18473249·Hemoglobin·2008
8-other
Three new beta-globin gene promoter mutations identified through newborn screening.
PMID 17486493·Hemoglobin·2007
5-case
Characterisation of a novel 49.3 kb Ggamma(Agamma delta beta)(0) -thalassaemia deletion in seven families of Asian descent.
PMID 17555456·Br J Haematol·2007
8-other
Prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLOS) by DHCR7 mutation analysis.
PMID 17441222·Prenat Diagn·2007
8-other
De novo mutation of the DHCR7 gene in a fetus with severe Smith-Lemli-Opitz (or RSH) syndrome.
PMID 17595012·Am J Med Genet A·2007
5-case
High oxygen affinity hemoglobin variant in a Canadian family: Hb Bunbury [beta94(FG1)Asp-->Asn, GAC-->AAC].
PMID 17365011·Hemoglobin·2007
5-case
Three new alpha-thalassemia point mutations ascertained through newborn screening.
PMID 16798638·Hemoglobin·2006
5-case
Economic impact of workplace productivity losses due to allergic rhinitis compared with select medical conditions in the United States from an employer perspective.
PMID 16846553·Curr Med Res Opin·2006
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 721 FAIRFAX AVE
NORFOLK, VA 23507 - Phone
- (757) 446-5955
Quick Facts
- NPI
- 1992779144
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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