Results 271 to 280 of about 33,888 (298)
Some of the next articles are maybe not open access.
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
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
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
Recidivism After Endoscopic Treatment of Cholesteatoma.
Otology and Neurotology, 2019OBJECTIVE To investigate the recidivism rate of cholesteatoma treated via endoscopic ear surgery (EES), either via transcanal endoscopic ear surgery or endoscopic assisted tympanomastoidectomy compared with a microscopic postauricular approach.
Daniel E. Killeen +4 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
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 ...
openaire +2 more sources
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 ...
openaire +2 more sources
Journal of the American Academy of Nurse Practitioners, 1990
Peter D. Phelps, Glyn A. S. Lloyd
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Peter D. Phelps, Glyn A. S. Lloyd
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Minerva urologica e nefrologica = The Italian journal of urology and nephrology, 1991
Renal cholesteatoma is an extremely uncommon disease. The renal pelvis is the most common site, but the lesion can be localized, even if rarely, in a calix or in the ureter. Histologically it consists of a keratinizing desquamative squamous metaplasia, with absence of cellular atypia in the urothelium, therefore cholesteatoma is not considered as a ...
LIBERTI, Marcello +4 more
openaire +2 more sources
Renal cholesteatoma is an extremely uncommon disease. The renal pelvis is the most common site, but the lesion can be localized, even if rarely, in a calix or in the ureter. Histologically it consists of a keratinizing desquamative squamous metaplasia, with absence of cellular atypia in the urothelium, therefore cholesteatoma is not considered as a ...
LIBERTI, Marcello +4 more
openaire +2 more sources