Results 201 to 210 of about 129,073 (257)
Balance Confidence and Falls in Individuals With Charcot-Marie-Tooth Disease: A Cross-Sectional Observational Study. [PDF]
Anderson KM +4 more
europepmc +1 more source
Clinical Characteristics of Gait Disturbance in Charcot-Marie-Tooth Disease and Future Directions in Physical Therapy. [PDF]
Kikuchi K.
europepmc +1 more source
Oesophageal Dysmotility in a Patient with Charcot-Marie-Tooth Disease: Report and Literature Review. [PDF]
Kloub M +6 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
Journal of the Peripheral Nervous System, 2011
Charcot‐Marie‐Tooth (CMT) disease is the commonest inherited neuromuscular disorder affecting at least 1 in 2,500. Over the last two decades, there have been rapid advances in understanding the molecular basis for many forms of CMT with more than 30 causative genes now described.
Reilly, Mary M +2 more
openaire +3 more sources
Charcot‐Marie‐Tooth (CMT) disease is the commonest inherited neuromuscular disorder affecting at least 1 in 2,500. Over the last two decades, there have been rapid advances in understanding the molecular basis for many forms of CMT with more than 30 causative genes now described.
Reilly, Mary M +2 more
openaire +3 more sources
JAMA, 1964
Peroneal muscular atrophy (Charcot-Marie-Tooth disease) in nine children often demonstrated characteristic, if not diagnostic, clinical features. A positive family history was highly suggestive. Biopsy specimens from two patients were of no value. Electromyelographic studies were not characteristic, but motor nerve conduction velocity studies done on ...
C W, DAWSON, J B, ROBERTS
openaire +2 more sources
Peroneal muscular atrophy (Charcot-Marie-Tooth disease) in nine children often demonstrated characteristic, if not diagnostic, clinical features. A positive family history was highly suggestive. Biopsy specimens from two patients were of no value. Electromyelographic studies were not characteristic, but motor nerve conduction velocity studies done on ...
C W, DAWSON, J B, ROBERTS
openaire +2 more sources

