Dr. Mauricio Javier Trujillo M.D.
Emergency Physician
3663 S Miami Ave Miami FL, 33133About
Dr. Mauricio Trujillo practices Emergency Medicine in Miami, FL. Dr. Trujillo assesses patients who seek immediate medical attention at any time of day or night. Emergency Medicine Physicians are trained to efficiently work with each patient and situation no matter how acute or life-threatening. Dr. Trujillo examines patients, determines means of testing, diagnoses conditions, and decides the best treatment methods.
Education and Training
Univ of Miami Sch of Med, Miami Fl 2000
University of Miami Leonard M. Miller School of Medicine 2000
Board Certification
Emergency MedicineAmerican Board of Emergency MedicineABEM- Undersea and Hyperbaric Medicine
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Retinitis pigmentosa, mental retardation, marked short stature, and brachydactyly in two sibs.
- Identification of three novel mutations in the MYO7A gene.
- Three novel RDS-peripherin mutations (689delT, 857del17, G208D) in Spanish families affected with autosomal dominant retinal degenerations. Mutations in brief no. 147. Online.
- First mutation (S340X) in choroideremia gene in a Spanish family. Mutations in brief no. 173. Online.
- Identification of two rare variants (G-->A at nucleotide 721; C-->T at nucleotide 5200) in the rhodopsin gene. Mutations in brief no. 187. Online.
- Three novel mutations (P215L, T289P, and 3811-2 A-->G) in the rhodopsin gene in autosomal dominant retinitis pigmentosa in Spanish families.
- Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2).
- Choroideremia, sensorineural deafness, and primary ovarian failure in a woman with a balanced X-4 translocation.
- A MELAS phenotype and a paternal inherited inversion of chromosome 10 in a female patient.
- Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) family.
- Two novel mutations (Y141H; C214Y) and previously published mutation (R142W) in the RDS-peripherin gene in autosomal dominant macular dystrophies in Spanish families.
- [Asp-190-Tyr mutation in the rhodopsin gene in a Spanish family with autosomic dominant pigmentary retinosis].
- [Retinitis pigmentosa, pattern dystrophy and fundus flavimaculatus not related to mutations in rhodopsine, peripherin/RDS and ROM-1 genes].
- Facets: computer software for evaluating assessment tools.
- Allergy to calcitonin.
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