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DUC VU, M.D.
M.D.
Neurology Physician
NPI: 1821431479IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
A135611(CA)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
CMS Specialties
PrimaryNEUROLOGY
Education
JEFFERSON MEDICAL COLLEGE OF THOMAS JEFFERSON UNIVERSITY
Class of 2012
Research & Publications (20)
Pseudohepatic cavernous hemangioma resulting from a prominent left portal vein of a portal systemic shunt collateral on Tc-99m SPECT red blood cell scintigraphy.
PMID 11290900·Clin Nucl Med·2001
5-case
Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants.
PMID 18223281·Haematologica·2008
7-preclinical
Quality of life evaluation for patients receiving vascularized versus nonvascularized bone graft reconstruction of segmental mandibular defects.
PMID 18718392·J Oral Maxillofac Surg·2008
4-observational
Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins.
PMID 17635718·J Thromb Haemost·2007
6-review
Safety and tolerability of oseltamivir prophylaxis in hematopoietic stem cell transplant recipients: a retrospective case-control study.
PMID 17578777·Clin Infect Dis·2007
8-other
Priming for immunologic memory in adults by meningococcal group C conjugate vaccination.
PMID 16760316·Clin Vaccine Immunol·2006
3-trial
Effectiveness analyses may underestimate protection of infants after group C meningococcal immunization.
PMID 16779730·J Infect Dis·2006
8-other
Antibody persistence 3 years after immunization of adolescents with quadrivalent meningococcal conjugate vaccine.
PMID 16479517·J Infect Dis·2006
2-rct
Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion.
PMID 16141000·J Med Genet·2005
5-case
Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia.
PMID 16195396·Hum Mol Genet·2005
4-observational
Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.
PMID 12893758·Blood·2003
5-case
Examination of the folding of E. coli CspA through tryptophan substitutions.
PMID 11567094·Protein Sci·2001
8-other
Developmental changes in cerebral white matter microstructure in a disorder of lysosomal storage.
PMID 19427638·Cortex·2010
8-other
Neisseria sicca/subflava bacteremia presenting as cutaneous nodules in an immunocompromised host.
PMID 19483662·Pediatr Infect Dis J·2009
5-case
NF-kappaB p52:RelB heterodimer recognizes two classes of kappaB sites with two distinct modes.
PMID 19098713·EMBO Rep·2009
7-preclinical
CD133+ endothelial progenitor cells as a potential cell source for a bioartificial glomerulus.
PMID 19358628·Tissue Eng Part A·2009
8-other
Regulation of Rxfp2 (Lgr8) expression in the mouse fetal kidney by the transcription factor Pod1 (Tcf 21).
PMID 19416211·Ann N Y Acad Sci·2009
7-preclinical
Anatomy of the subtalar joint and imaging of talo-calcaneal coalition.
PMID 19096839·Skeletal Radiol·2009
6-review
Dual-beam Fourier domain optical Doppler tomography of zebrafish.
PMID 18772973·Opt Express·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 101 THE CITY DR S
ORANGE, CA 92868 - Phone
- (714) 456-7890
Quick Facts
- NPI
- 1821431479
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 14
- Publications
- 20
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