Clinical Focus

  • Pulmonary Critical Care
  • Pulmonary Disease

Academic Appointments

Administrative Appointments

  • Cystic Fibrosis Director of Outpatient Services, SUMC (2008 - 2009)
  • Member, North American Cystic Fibrosis Foundation (2005 - Present)
  • Member, California Thoracic Society (2003 - Present)
  • Member, American Thoracic Society (2002 - Present)
  • Member, American College of Chest Physicians (2002 - Present)
  • Ethics Committee, SUMC (2006 - 2009)
  • Code Team Committee, SUMC (2009 - 2009)
  • Director Adult Cystic Firbosis, SUMC (2005 - 2008)
  • Member, Society of Critical Care Medicine (2005 - Present)

Honors & Awards

  • Teaching Award, Division Pulmonary and Critical Care (2007)

Professional Education

  • Board Certification: Critical Care Medicine, American Board of Internal Medicine (2006)
  • Residency:Michigan State University (2002) MI
  • Board Certification: Pulmonary Disease, American Board of Internal Medicine (2005)
  • Fellowship:Stanford University Medical Center (2005) CA
  • Fellowship:California Pacific Medical Center (2004) CA
  • Internship:Michigan State University (2000) MI
  • Medical Education:Ross University School of Medicine (1998) NJ
  • B.S., University of Toronto- Ontario, Chemistry & Zoology (Human Physiology) (1994)
  • MD, Ross University, Internal Medicine (1999)
  • Pulmonary Fellowship, California Pacific Med Center, Pulmonary Medicine (2004)
  • Critical Care Fellowship, Stanford University, Critical Care Medicine (2005)

Research & Scholarship

Clinical Trials

  • Rare Genetic Disorders of the Breathing Airways Recruiting

    Mucociliary clearance, in which mucus secretions are cleared from the breathing airways, is the primary defense mechanism for the lungs. Inhaled particles, including microbes that can cause infections, are normally entrapped in mucus on the airway surfaces and then cleared out by the coordinated action of tiny hair-like structures called cilia. Individuals with primary ciliary dyskinesia, variant cystic fibrosis, and pseudohypoaldosteronism have defective mucociliary clearance. The purpose of this study is to collect clinical and genetic information about these three airway diseases to improve current diagnostic procedures.

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2015-16 Courses