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Archives of Otolaryngology - Head and Neck Surgery, 1972
The temporal bone findings from two patients with Mondini's genetic aplastic deafness are described. Profound sensorineural deafness was present in both cases and audiology and speech studies were available for the first patient. Cochlear changes which were similar for both, consisted of a flattened cochlear capsule, 1½ instead of 2½ cochlear turns ...
M M, Paparella, F M, el-Fiky
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The temporal bone findings from two patients with Mondini's genetic aplastic deafness are described. Profound sensorineural deafness was present in both cases and audiology and speech studies were available for the first patient. Cochlear changes which were similar for both, consisted of a flattened cochlear capsule, 1½ instead of 2½ cochlear turns ...
M M, Paparella, F M, el-Fiky
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JAMA: The Journal of the American Medical Association, 1971
To the Editor.— I wonder if anyone has considered the possibility of Paget's disease of the bone as the cause of Beethoven's deafness. At postmortem examination his skull was "of great density and a thickness amounting to about half an inch." If he had had this condition, death could conceivably have been due to high output heart failure.
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To the Editor.— I wonder if anyone has considered the possibility of Paget's disease of the bone as the cause of Beethoven's deafness. At postmortem examination his skull was "of great density and a thickness amounting to about half an inch." If he had had this condition, death could conceivably have been due to high output heart failure.
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Clinical Genetics, 2007
Non‐syndromic deafness can be caused by mutations in both nuclear and mitochondrial genes. More than 50 nuclear genes have been shown to be involved in non‐syndromic hearing loss, but mutations in mitochondrial DNA (mtDNA) might also cause hearing impairment.
H, Kokotas, M B, Petersen, P J, Willems
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Non‐syndromic deafness can be caused by mutations in both nuclear and mitochondrial genes. More than 50 nuclear genes have been shown to be involved in non‐syndromic hearing loss, but mutations in mitochondrial DNA (mtDNA) might also cause hearing impairment.
H, Kokotas, M B, Petersen, P J, Willems
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Veterinary Clinics of North America: Small Animal Practice, 2012
Conductive deafness, caused by outer or middle ear obstruction, may be corrected, whereas sensorineural deafness cannot. Most deafness in dogs is congenital sensorineural hereditary deafness, associated with the genes for white pigment: piebald or merle. The genetic cause has not yet been identified.
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Conductive deafness, caused by outer or middle ear obstruction, may be corrected, whereas sensorineural deafness cannot. Most deafness in dogs is congenital sensorineural hereditary deafness, associated with the genes for white pigment: piebald or merle. The genetic cause has not yet been identified.
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Nursing Standard, 1994
The third edition of the 199415 Directory from the Council for the Advancement of Communication with Deaf People (CACDP) is now available. Information on 192 sign language interpreters, lipspeakers, interpreters for deafblind people and speech to text reporters is provided. Details from CACDP on 0191 374 3607.
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The third edition of the 199415 Directory from the Council for the Advancement of Communication with Deaf People (CACDP) is now available. Information on 192 sign language interpreters, lipspeakers, interpreters for deafblind people and speech to text reporters is provided. Details from CACDP on 0191 374 3607.
openaire +2 more sources