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HENRY ALEXANDER ARTS MD
MD
Otology & Neurotology Physician
NPI: 1801983655IndividualAccepts Medicare
Specialties, Licenses & Credentials
Otolaryngology Physician
Otolaryngology
Code: 207Y00000X
4301062152(MI)39186(AL)
Otology & Neurotology PhysicianPrimary
Otolaryngology — Otology & Neurotology
Code: 207YX0901X
39186(AL)4301062152(MI)
Education
BAYLOR COLLEGE OF MEDICINE
Class of 1983
Research & Publications (20)
Reversible electrocochleographic abnormalities in superior canal dehiscence.
PMID 19092559·Otol Neurotol·2009
8-other
Hearing preservation and facial nerve outcomes in vestibular schwannoma surgery: results using the middle cranial fossa approach.
PMID 16436995·Otol Neurotol·2006
8-other
Prosthetic stimulation of the auditory system with intraneural electrodes.
PMID 14533840·Ann Otol Rhinol Laryngol Suppl·2003
7-preclinical
Time to stop ovarian cancer screening in BRCA1/2 mutation carriers?
PMID 19035463·Int J Cancer·2009
8-other
Total laparoscopic hysterectomy versus abdominal hysterectomy in the treatment of patients with early stage endometrial cancer: a randomized multi center study.
PMID 19146684·BMC Cancer·2009
3-trial
Autoantibodies to recombinant human CTL2 in autoimmune hearing loss.
PMID 19319905·Laryngoscope·2009
8-other
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290.
PMID 18950740·Am J Hum Genet·2008
8-other
Endotoxin exposure in sewage treatment workers: investigation of exposure variability and comparison of analytical techniques.
PMID 19118445·Ann Agric Environ Med·2008
4-observational
Role of electrically evoked auditory brainstem response in cochlear implantation of children with inner ear malformations.
PMID 18520627·Otol Neurotol·2008
8-other
Cochlin isoforms and their interaction with CTL2 (SLC44A2) in the inner ear.
PMID 17926100·J Assoc Res Otolaryngol·2007
7-preclinical
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
PMID 17558407·Nat Genet·2007
7-preclinical
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.
PMID 17546029·Nat Genet·2007
7-preclinical
High percentage of abnormal findings on TVU needs further discussion.
PMID 17047659·Br J Cancer·2006
8-other
Influence of different cleaning practices on endotoxin exposure at sewage treatment plants.
PMID 16782738·Ann Occup Hyg·2006
8-other
Transient evoked otoacoustic emissions pattern as a prognostic indicator for hearing preservation in acoustic neuroma surgery.
PMID 16639277·Otol Neurotol·2006
8-other
Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations.
PMID 16339905·Proc Natl Acad Sci U S A·2005
7-preclinical
Fas and Fas ligand in cyst fluids, serum and tumors of patients with benign and (borderline) malignant ovarian tumors.
PMID 15645122·Int J Oncol·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 1500 EAST MEDICAL CENTER DR, 1ST FLOOR TAUBMAN CTR RECP A
ANN ARBOR, MI 48109 - Phone
- (734) 936-8051
Quick Facts
- NPI
- 1801983655
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 3
- Years in Practice
- 43
- Publications
- 20
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