Professor, Otolaryngology/Head and Neck Surgery, University of Cincinnati College of Medicine
Otolaryngology (ENT)
Dr. John H. Greinwald, MD
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John H. Greinwald, MD is an expert in the field of Otolaryngology (ENT). He graduated from Medical University of South Carolina College of Medicine. He has 2 awards "Fellow (FAAO-HNS)" and "Fellow (FAAP)". Dr. John H. Greinwald is also a published doctor. He has 76 publication published. The most recent publication is: An update on the treatment of hemangiomas in children with interferon alfa-2a.
Publications
- High-frequency sensorineural Hearing loss in children.
- Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 Hearing loss.
- Codeine-related adverse drug reactions in children following tonsillectomy: A prospective study.
- Genetic Analysis through OtoSeq of Pakistani Families Segregating Prelingual Hearing Loss.
- Performance Evaluation of the Next-Generation Sequencing Approach for Molecular Diagnosis of Hereditary Hearing Loss.
- Significance of unilateral enlarged vestibular aqueduct.
- Characteristics of children diagnosed as having coagulopathies following posttonsillectomy bleeding.
- Genetic mutations and aminoglycoside-induced ototoxicity in neonates.
- H1N1 influenza A presenting as bacterial tracheitis.
- Neuroanatomic differences in children with unilateral sensorineural Hearing loss detected using functional magnetic resonance imaging.
- An overview of custom array sequencing.
- Audiologic and temporal bone imaging findings in patients with sensorineural Hearing loss and GJB2 mutations.
- Aminoglycoside ototoxicity in Nicaraguan children: patient risk factors and mitochondrial DNA results.
- The role of CMV inflammatory genes in Hearing loss.
- Macrophage inflammatory proteins in cytomegalovirus-related inner ear injury.
- A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort.
- Prevalence and etiology of Hearing loss in rural Nicaraguan children.
- 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 an...
- Improved diagnostic effectiveness with a sequential diagnostic paradigm in idiopathic pediatric sensorineural Hearing loss.
- Extremely low penetrance of Hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
- Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.
- A diagnostic paradigm for childhood idiopathic sensorineural Hearing loss.
- Bacterial tracheitis reexamined: is there a less severe manifestation?
- Co-expression of pendrin, vacuolar H+-ATPase alpha4-subunit and carbonic anhydrase II in epithelial cells of the murine endolymphatic sac.
- The cochlear cleft.
- Temporal bone abnormalities associated with Hearing loss in Waardenburg syndrome.
- Genotypic and phenotypic correlations of DFNB1-related Hearing impairment in the Midwestern United States.
- Expression of aquaporin 1 and 5 in the developing mouse inner ear and audiovestibular assessment of an Aqp5 null mutant.
- Adult laryngomalacia: an uncommon clinical entity.
- Treatment of lymphangiomas with OK-432 (Picibanil) sclerotherapy: a prospective multi-institutional trial.
- Clinical and audiological features in auditory neuropathy.
- Ectopic cervical thymus: an uncommon diagnosis in the evaluation of pediatric Neck masses.
- The evaluation of children with sensorineural Hearing loss.
- When is the vestibular aqueduct enlarged? A statistical analysis of the normative distribution of vestibular aqueduct size.
- GJB2 mutations and additional disabilities in a pediatric cochlear implant population.
- Management of massive Head and neck neurofibromas in children.
- Absorption of topical cocaine in rhinologic procedures.
- Hereditary thyrogLossal duct cysts.
- Lipomas of the internal auditory canal.
- Pathologic quiz case 2. Congenital cartilaginous rests of the Neck (CCRNs) (wattles).
- Electrocautery versus carbon dioxide laser for uvulopalatoplasty in the treatment of snoring.
- Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.
- Thoracic duct injury during anterior cervical discectomy: a rare complication. Case report.
- Presymptomatic diagnosis of nonsyndromic Hearing loss by genotyping.
- Refined mapping of a gene for autosomal dominant progressive sensorineural Hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed i...
- Diagnosis and management of middle ear osteomas: a case report and literature review.
- Localization of a novel gene for nonsyndromic Hearing loss (DFNB17) to chromosome region 7q31.
- Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn Hearing-loss loci on human chromosome 9q and mouse chromo...
- An update on the treatment of hemangiomas in children with interferon alfa-2a.
- Effects of dimethylthiourea, melatonin, and hyperbaric oxygen therapy on the survival of reimplanted rabbit auricular composite grafts.
- Treatment of lymphangiomas in children: an update of Picibanil (OK-432) sclerotherapy.
- Laryngomalacia and its treatment.
- Larsen's syndrome.
- Effect of pentoxifylline on the healing of guinea pig tympanic membrane.
- Endobronchial tumors in children: an uncommon clinical entity.
- Simulated Reflux and laryngotracheal reconstruction: a rabbit model.
- Nontraumatic atlantoaxial rotary subluxation in the pediatric otolaryngology patient. A report of four cases.
- Audiometric, clinical and educational outcomes in a pediatric symptomatic congenital cytomegalovirus (CMV) population with sensorineural Hearing loss.
- Optimal concentration of epinephrine for vasoconstriction in ear surgery.
- Pediatric cochlear implantation in auditory neuropathy.
- Cortical reorganization in children with unilateral sensorineural Hearing loss.
- Genomic organization and expression analysis of the murine Fam3c gene.
- Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic Hearing loss.
- Refining the DFNB17 interval in consanguineous Indian families.
- Enlarged vestibular aqueduct syndrome in the pediatric population.
- Molecular mechanisms underlying inner ear patterning defects in kreisler mutants.
- The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct.
- The large vestibular aqueduct: a new definition based on audiologic and computed tomography correlation.
- Hearing loss progression and contralateral involvement in children with unilateral sensorineural Hearing loss.
- A rapid method for detection of five known mutations associated with aminoglycoside-induced Deafness.
- Massive lymphatic malformations of the Head, neck, and chest.
- Maternally inherited aminoglycoside-induced and nonsyndromic Hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.
- High-throughput detection of mutations responsible for childhood Hearing loss using resequencing microarrays.
- Peritonsillar abscess: an unlikely cause of necrotizing fasciitis.
- Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital Hearing loss.
Schools
Medical University of South Carolina
Naval Hospital
Naval Med Center
University Iowa
Procedures Preformed
- Cochlear Implant Insertion
- Ear Tube Placement
- Excision or Destruction of Tongue Lesion
- Intranasal or Sinus Procedure
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Conditions Treated
- Acoustic Neuroma
- Cholesteatoma
- Chronic Sinusitis
- Conductive Hearing Loss
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Doctors Specialties
- Ear, Nose, and Throat
- Otolaryngology (ENT)
Accepted Insurances
Awards
- Fellow (FAAO-HNS)
- Fellow (FAAP)
Education
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Naval Medical Center -
Medical University of South Carolina College of Medicine
Hospital
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Cincinnati Children's Hospital Medical Center
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