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GABRIELLE BRICE, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1629798798Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.
PMID 12114478·J Med Genet·2002
8-other
Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.
PMID 19002718·Hum Genet·2009
8-other
Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2.
PMID 18197197·Eur J Hum Genet·2008
8-other
Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.
PMID 17932119·J Med Genet·2008
8-other
A new locus (GLC1H) for adult-onset primary open-angle glaucoma maps to the 2p15-p16 region.
PMID 17210857·Arch Ophthalmol·2007
8-other
Three children with Milroy disease and de novo mutations in VEGFR3.
PMID 17250670·Clin Genet·2007
5-case
A family with lymphoedema-distichiasis where identical twins have a discordant phenotype.
PMID 17309653·Clin Genet·2007
8-other
Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb.
PMID 17372167·Circulation·2007
8-other
The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193 FBN1 mutations.
PMID 17657824·Hum Mutat·2007
8-other
Respiratory virus panels for global surveillance of emerging infectious diseases.
PMID 18162260·J Clin Virol·2007
6-review
The US capitol bioterrorism anthrax exposures: clinical epidemiological and immunological characteristics.
PMID 17191162·J Infect Dis·2007
8-other
Extended immunization intervals enhance the immunogenicity and protective efficacy of plasmid DNA vaccines.
PMID 17913540·Microbes Infect·2007
7-preclinical
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.
PMID 16389592·Am J Med Genet B Neuropsychiatr Genet·2006
8-other
Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutations.
PMID 15906099·Hum Genet·2005
8-other
Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin gene.
PMID 16043855·Invest Ophthalmol Vis Sci·2005
8-other
Influence of contraction velocity in untrained individuals over the initial early phase of resistance training.
PMID 16287371·J Strength Cond Res·2005
2-rct
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2301 ERWIN ROAD
DURHAM, NC 27710 - Phone
- (919) 684-8111
Quick Facts
- NPI
- 1629798798
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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