Results 221 to 230 of about 27,612 (251)
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Archives of Otolaryngology - Head and Neck Surgery, 1995
To review the characteristics of congenital cholesteatomata.Case series.Tertiary care (referral-based) private practice.Fourteen patients were included in the study. The diagnosis of congenital cholesteatoma was based on an intact tympanic membrane on physical examination; a history that excluded tympanic membrane perforation, otorrhea, or previous ...
J J, Zappia, R J, Wiet
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To review the characteristics of congenital cholesteatomata.Case series.Tertiary care (referral-based) private practice.Fourteen patients were included in the study. The diagnosis of congenital cholesteatoma was based on an intact tympanic membrane on physical examination; a history that excluded tympanic membrane perforation, otorrhea, or previous ...
J J, Zappia, R J, Wiet
openaire +2 more sources
Endoscopic Versus Microscopic Management of Attic Cholesteatoma: A Randomized Controlled Trial
The Laryngoscope, 2019To compare endoscopic transcanal approach to attic cholesteatoma with conventional microscopic transcanal ...
Arindam Das +3 more
semanticscholar +1 more source
Pediatric Annals, 2016
Congenital cholesteatoma is one of the more common causes of the onset of childhood conductive hearing loss unrelated to middle ear effusion. If undiagnosed, the disease can progress to irreversibly destroy the conductive hearing architecture, as well as the surrounding skull base of the lateral temporal bone.
David, Walker, Michael J, Shinners
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Congenital cholesteatoma is one of the more common causes of the onset of childhood conductive hearing loss unrelated to middle ear effusion. If undiagnosed, the disease can progress to irreversibly destroy the conductive hearing architecture, as well as the surrounding skull base of the lateral temporal bone.
David, Walker, Michael J, Shinners
openaire +2 more sources
Otology and Neurotology, 2019
OBJECTIVE Assessment of validity of the Japanese Otological Society and the European Academy of Otology and Neurotology (EAONO-JOS) cholesteatoma staging system (EJS) through international collaboration to investigate: (a) feasibility of retrospectively ...
A. James +9 more
semanticscholar +1 more source
OBJECTIVE Assessment of validity of the Japanese Otological Society and the European Academy of Otology and Neurotology (EAONO-JOS) cholesteatoma staging system (EJS) through international collaboration to investigate: (a) feasibility of retrospectively ...
A. James +9 more
semanticscholar +1 more source
Urology, 1988
Renal cholesteatoma is being reported more frequently in the literature. A case with a twenty-year documented history is presented, together with observations on differential diagnosis.
R P, Molina, D A, Dulabon, R B, Roth
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Renal cholesteatoma is being reported more frequently in the literature. A case with a twenty-year documented history is presented, together with observations on differential diagnosis.
R P, Molina, D A, Dulabon, R B, Roth
openaire +2 more sources
Otology and Neurotology, 2019
OBJECTIVES To evaluate non echo-planar diffusion weighted magnetic resonance imaging (non-EP DW MRI) at 9 months after primary surgery to rule out residual cholesteatoma in patients scheduled before second-look-surgical exploration.
R. J. Horn +4 more
semanticscholar +1 more source
OBJECTIVES To evaluate non echo-planar diffusion weighted magnetic resonance imaging (non-EP DW MRI) at 9 months after primary surgery to rule out residual cholesteatoma in patients scheduled before second-look-surgical exploration.
R. J. Horn +4 more
semanticscholar +1 more source
Otolaryngologic Clinics of North America
Congenital cholesteatoma is a cyst of keratinizing squamous cell epithelium in the setting of an intact tympanic membrane, in a patient without a history of otorrhea, tympanic membrane perforation, or otologic surgery. The most common presentation of a congenital cholesteatoma is that of an asymptomatic pearly white mass in the anterosuperior quadrant ...
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Congenital cholesteatoma is a cyst of keratinizing squamous cell epithelium in the setting of an intact tympanic membrane, in a patient without a history of otorrhea, tympanic membrane perforation, or otologic surgery. The most common presentation of a congenital cholesteatoma is that of an asymptomatic pearly white mass in the anterosuperior quadrant ...
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International Journal of Pediatric Otorhinolaryngology, 2021
G. Piras +6 more
semanticscholar +1 more source
G. Piras +6 more
semanticscholar +1 more source
Microbiome Analysis of Cholesteatoma by Gene Sequencing.
Otology and Neurotology, 2019OBJECTIVE To compare the microbial flora of cholesteatoma and normal middle ears using gene-based sequencing analysis. STUDY DESIGN Controlled ex vivo human study. SETTING Academic, tertiary medical center.
Joshua P. Weiss +2 more
semanticscholar +1 more source

