Dr. David Michael Roden M.D.
Ear-Nose and Throat Doctor (ENT)
2520 Mccandless Dr Midland MI, 48640About
Dr. David Roden is an ear, nose and throat (ENT) doctor, also known as an otolaryngologist, practicing in Midland, MI. Dr. Roden specializes in diseases and disorders of the ear, nose and throat as well as other parts of the head and neck. Such structures an ENT may work on include the sinuses, larynx (voice box) and mouth in addition to the ear, nose and throat. There are seven areas of expertise that an ENT might specialize in, and these are: allergies; facial reconstructive surgery; head and neck; laryngology; otology/neurotology; pediatric otolaryngology; and rhinology.
Education and Training
Univ of Mi Med Sch, Ann Arbor Mi 1990
Board Certification
OtolaryngologyAmerican Board of OtolaryngologyABOto
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Drug-induced J point elevation: a marker for genetic risk of sudden death or ECG curiosity?
- Calmodulin kinase inhibition prevents development of the arrhythmogenic transient inward current.
- Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.
- Modulation of effect of dietary salt on prehepatic first-pass metabolism: effects of beta-blockade and intravenous salt loading.
- Exaggerated QT prolongation after cardioversion of atrial fibrillation.
- An overview of contemporary approaches to antiarrhythmic therapy.
- A spotlight on electrophysiological remodeling and the molecular biology of ion channels.
- From genes to channels: normal mechanisms.
- Mechanisms underlying variability in response to drug therapy: implications for amiodarone use.
- Impact of recent molecular studies on evaluation of ventricular arrhythmias.
- Systemic administration of calmodulin antagonist W-7 or protein kinase A inhibitor H-8 prevents torsade de pointes in rabbits.
- A plethora of mechanisms in the HERG-related long QT syndrome. Genetics meets electrophysiology.
- Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X.
- The long QT syndromes: genetic basis and clinical implications.
- Congenital and acquired long QT syndrome.
Dr. David Michael Roden M.D.'s Practice location
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