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Larissa V. Furtado, M.D. - Pathology Resident

last modified 2009-08-04 16:39 — by Amy Motta

Larissa V. Furtado, M.D.

Larissa Furtado, M.D.

Rank: PGY- 2

Residency Program: AP/CP

Contact Info

Email Address: larissa.furtado {AT} aruplab.com

Office Phone Number: 801-587-4281

Pager Number: 339-9734

Location:   University of Utah Hospital

Division: Residency Program

 

Professional Education

  • 2008, Clinical Biochemical Genetics Fellowship, University of Utah/ARUP Laboratories, Salt Lake City, Utah
  • 2006, Medical Genetics Residency, Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto - Universidade de Sao Paulo (University of Sao Paulo), Ribeirao Preto SP, Brazil
  • 2002, Medical Internship, Hospital of Santa Casa de Misericordia, Goiania GO, Brazil
  • 2002, M.D. Centro Universitario de Volta Redonda (Central University of Volta Redonda) (UNIFOA), former Escuela de Ciencias Medicas de Volta Redonda, Volta Redonda RJ, Brazil

Presentations

  • Male Infant with ectodermal and biochemical phenotype of CDPX2 without chondrodysplasia punctata, Poster, 28th Annual David W. Smith Workshop on Malformations and Morphogenesis, Williamsburg, Virginia, August, 2007
  • Trissomy 18 syndrome in a girl with 13 year old: a case report, Poster, The Brazilian Society of Clinical Genetics XVII Annual Meeting, Curitiba, Brazil, June, 2005
  • Differential Diagnosis between Joubert Syndrome and Dysequilibrium Syndrome: a case report, Poster, The Brazilian Society of Clinical Genetics XVII Annual Meeting, Curitiba, Brazil, June, 2005
  • Chromosome-phenotype correlations in a carrier of a ring 18 chromosome, Poster, The Brazilian Society of Genetics 50th Annual Meeting, Florianopolis, Brazil, September, 2004
  • A case report of a Brazilian family with triphalangeal thumb-brachyectrodactyly syndrome, Poster, The Brazilian Society of Clinical Genetics XVI Annual Meeting, Belem, Brazil, June, 2004
  • Analysis of electroencephalogram and epilepsy in Lowe Syndrome, Poster, XXIX Brazilian Epilepsy Congress and XV Brazilian Clinical Neurophysiology Meeting, Ribeirao Preto, Brazil, June, 2004
  • Hyperammonemia due to valproate: Differential diagnosis with urea cycle disorder, Poster, XXIX Brazilian Epilepsy Congress and XV Brazilian Clinical Neurophysiology Meeting, Ribeirao Preto, Brazil, June, 2004
  • Daltonism and Turner Syndrome: A case report of a X-linked recessive syndrome in this patient, Poster, The Brazilian Society of Clinical Genetics XVI Annual Meeting, Belem, Brazil, June, 2004
  • Yellow Nail Syndrome: Evidence of autossomal recessive trait, Poster, The American Society of Human Genetics (ASHG) 53rd Annual Meeting, Los Angeles, California, November, 2003
  • Meier-Gorlin Syndrome: A Brazilian case report, Poster, The Brazilian Society of Clinical Genetics XV Annual Meeting, Porto, Alegre, Brazil, June, 2003
  • Neonatal bone dysplasias: Uncommon and definitely important, Poster, The Brazilian Society of Clinical Genetics XV Annual Meeting, Porto Alegre, Brazil, June, 2003
  • Comparative analysis of prostatic mapping through biopsy with six and twelve prostatic fragments guided by ultrasound, Poster, IV Scientific Meeting of Medical Doctors and Medical Students of Santa Casa de Misericordia de Goiania, Goiania, Brazil, September, 2002
  • Epidemiological Profile of patients assisted in prostatic biopsy in the Hospital of Santa Casa de Misericordia de Goiania, Poster, IV Scientific Meeting of Medical Doctors and Medical Students of Santa Casa de Misericordia de Goiania, Goiania, Brazil, September, 2002