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JOHN GREINWALD, M.D.
M.D.
Pediatric Otolaryngology Physician
NPI: 1275547457IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatric Otolaryngology PhysicianPrimary
Otolaryngology — Pediatric Otolaryngology
Code: 207YP0228X
35.077959(OH)
CMS Specialties
PrimaryOTOLARYNGOLOGY
Education
MEDICAL UNIVERSITY OF SOUTH CAROLINA COLLEGE OF MEDICINE
Class of 1987
Research & Publications (20)
Massive lymphatic malformations of the head, neck, and chest.
PMID 19128607·J Otolaryngol Head Neck Surg·2008
8-other
The evaluation of children with sensorineural hearing loss.
PMID 11784264·Arch Otolaryngol Head Neck Surg·2002
8-other
A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness.
PMID 19144107·BMC Med Genet·2009
8-other
Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations.
PMID 19235794·Laryngoscope·2009
4-observational
Aminoglycoside ototoxicity in Nicaraguan children: patient risk factors and mitochondrial DNA results.
PMID 19130971·Otolaryngol Head Neck Surg·2009
8-other
Macrophage inflammatory proteins in cytomegalovirus-related inner ear injury.
PMID 17903579·Otolaryngol Head Neck Surg·2007
7-preclinical
The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct.
PMID 17309986·Arch Otolaryngol Head Neck Surg·2007
8-other
Prevalence and etiology of hearing loss in rural Nicaraguan children.
PMID 17334299·Laryngoscope·2007
6-review
The large vestibular aqueduct: a new definition based on audiologic and computed tomography correlation.
PMID 17547990·Otolaryngol Head Neck Surg·2007
8-other
Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.
PMID 17698299·Gene·2007
8-other
A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort.
PMID 17666888·Genet Med·2007
4-observational
GJB2 mutations and additional disabilities in a pediatric cochlear implant population.
PMID 16154643·Int J Pediatr Otorhinolaryngol·2006
8-other
Molecular mechanisms underlying inner ear patterning defects in kreisler mutants.
PMID 16325169·Dev Biol·2006
7-preclinical
Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
PMID 15708009·Biochem Biophys Res Commun·2005
8-other
Cortical reorganization in children with unilateral sensorineural hearing loss.
PMID 15770152·Neuroreport·2005
3-trial
Improved diagnostic effectiveness with a sequential diagnostic paradigm in idiopathic pediatric sensorineural hearing loss.
PMID 16015155·Otol Neurotol·2005
4-observational
Audiometric, clinical and educational outcomes in a pediatric symptomatic congenital cytomegalovirus (CMV) population with sensorineural hearing loss.
PMID 16061110·Int J Pediatr Otorhinolaryngol·2005
8-other
Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.
PMID 16152638·Am J Med Genet A·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 3333 BURNET AVE, ML 2018
CINCINNATI, OH 45229 - Phone
- (513) 636-4355
Quick Facts
- NPI
- 1275547457
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 39
- Publications
- 20
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