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BRENT CASTLE D.O.
D.O.
Emergency Medicine Physician
NPI: 1750677399IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
1750677399(OH)
Education
AT STILL UNIVERSITY OF HEALTH SCIENCES, COLLEGE OF OSTEO MED, KIRKSVILLE
Class of 2011
Research & Publications (16)
Phenotype and genotype in 17 patients with Goltz-Gorlin syndrome.
PMID 19586929·J Med Genet·2009
8-other
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
PMID 19372089·J Med Genet·2009
8-other
A simple and efficient approach to reversed-phase HPLC method screening.
PMID 19181471·J Pharm Biomed Anal·2009
8-other
ABCC6 mutations in pseudoxanthoma elasticum: an update including eight novel ones.
PMID 18253096·Mol Vis·2008
8-other
Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences.
PMID 17318843·Am J Med Genet A·2007
5-case
Language and literacy outcomes from a pilot intervention study for children with fetal alcohol spectrum disorders in South Africa.
PMID 17936509·Alcohol·2007
2-rct
Clinical features in a family with an R460H mutation in transforming growth factor beta receptor 2 gene.
PMID 16885183·J Med Genet·2006
8-other
Mid-trimester hyperechogenic bowel in a fetus of Japanese origin: caution in interpreting reported CFTR mutation (L548Q).
PMID 16941515·Prenat Diagn·2006
8-other
Sphingosine kinase 1 is a negative regulator of CD4+ Th1 cells.
PMID 16272312·J Immunol·2005
7-preclinical
BRCA1 mutation and neuronal migration defect: implications for chemoprevention.
PMID 15994867·J Med Genet·2005
5-case
BRCA1 mutation and neuronal migration defect: implications for chemoprevention.
PMID 15863656·J Med Genet·2005
5-case
Anophthalmia-esophageal-genital syndrome: a further case to define the phenotype.
PMID 15384104·Am J Med Genet A·2005
5-case
SHOX mutations in a family and a fetus with Langer mesomelic dwarfism.
PMID 15214013·Am J Med Genet A·2004
5-case
Expression of activation-induced cytidine deaminase in human B-cell non-Hodgkin lymphomas.
PMID 12511417·Blood·2003
4-observational
Evaluation of genotype-phenotype correlations in neurofibromatosis type 1.
PMID 14569132·J Med Genet·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
- 500 N RAINBOW BLVD STE 203
LAS VEGAS, NV 89107 - Phone
- (702) 259-1228
Quick Facts
- NPI
- 1750677399
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 15
- Publications
- 16
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