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Charcot-Marie-Tooth disease

Current Treatment Options in Neurology, 2008
The family of hereditary peripheral neuropathies that makes up Charcot-Marie-Tooth disease (CMT) comprises some of the most common neuromuscular disorders. Over the past decade, understanding of the molecular basis of CMT has increased enormously. In addition, the neurophysiologic deficits and clinical problems associated with CMT are more clearly ...
Gregory T, Carter   +4 more
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Periodontal diseases and tooth loss

Periodontology 2000, 1993
L Jackson Brown, R C Oliver, L J Brown
exaly   +3 more sources

Charcot-Marie-Tooth disease

The Journal of Pediatrics, 1953
Summary A review of Charcot-Marie-Toothdisease is presented with illustrative cases. This condition can be differentiated from other neuromuscular conditions and diagnosed at a relatively early stage. It is self-limiting and surgery is of great help in restoring the affected individual to a more normal way of life.
R T, LIDGE, F A, CHANDLER
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Tooth mobility and periodontal Disease

Journal of Clinical Periodontology, 1997
Abstract Tooth mobility (TM) is an important feature of periodontal disease. This is evidenced by the large number of devices and methods of TM assessment that have been developed and tested. TM had been considered and investigated as an indirect measure of the functional condition of the periodontium as well as possible aggravating co‐factor for ...
M, Giargia, J, Lindhe
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Charcot-Marie-Tooth Disease

Archives of Neurology, 1967
THE credit for discovering a "new disease" is often given not to the one who describes it first but to the one who describes it when the time is ripe. Thus, Virchow,1Schultze,2and others had reported cases of peroneal atrophy previously, but in 1886 medical knowledge had advanced sufficiently to accept this entity as a nosologic addition.
L A, Brody, R H, Wilkins
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