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BONAVENTURE ENG, MD
MD
Gastroenterology Physician
NPI: 1538366489Individual
Specialties, Licenses & Credentials
Gastroenterology PhysicianPrimary
Internal Medicine — Gastroenterology
Code: 207RG0100X
G22291(CA)
Research & Publications (20)
Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG).
PMID 19205977·Hemoglobin·2009
5-case
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
Frameshift mutation in the alpha2-globin gene causing alpha+ -thalassemia: codon 49 (-GC).
PMID 18473249·Hemoglobin·2008
8-other
Characterization of a long-term rat mTAL cell line.
PMID 17670898·Am J Physiol Renal Physiol·2007
7-preclinical
Three new beta-globin gene promoter mutations identified through newborn screening.
PMID 17486493·Hemoglobin·2007
5-case
Three new alpha-thalassemia point mutations ascertained through newborn screening.
PMID 16798638·Hemoglobin·2006
5-case
Characterization of a rare single alpha-globin gene deletion in a Chinese woman with Hb H disease.
PMID 16370493·Hemoglobin·2005
5-case
Identification of nine novel arylsulfatase a (ARSA) gene mutations in patients with metachromatic leukodystrophy (MLD).
PMID 14517960·Hum Mutat·2003
8-other
Detection of severe nondeletional alpha-thalassemia mutations using a single-tube multiplex ARMS assay.
PMID 11960579·Genet Test·2001
8-other
PCR-based diagnosis of the Filipino (--(FIL)) and Thai (--(THAI)) alpha-thalassemia-1 deletions.
PMID 10602170·Am J Hematol·2000
8-other
Hb North York [beta 117(G19)His-->Asp]: a new beta chain hemoglobin variant.
PMID 19205973·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
Characterisation of the British alpha 0-thalassaemia deletion: evidence of a founder effect in Newfoundland, Canada.
PMID 19622095·Br J Haematol·2009
8-other
Novel 27.9 kb alpha(0)-thalassemia deletion in a Filipino woman.
PMID 19195033·Am J Hematol·2009
5-case
Three new beta-thalassemia mutations with varying degrees of severity.
PMID 19657836·Hemoglobin·2009
5-case
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
Systematic analysis of outcomes evaluations applied to drug management programs.
PMID 18991480·Am J Manag Care·2008
1-meta
Prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLOS) by DHCR7 mutation analysis.
PMID 17441222·Prenat Diagn·2007
8-other
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
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2230 LYNN ROAD, SUITE 104
THOUSAND OAKS, CA 91360 - Phone
- (805) 497-0961
Quick Facts
- NPI
- 1538366489
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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