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Charcot-Marie-Tooth Disease

Archives of Neurology, 1963
Charcot-Marie-Tooth disease (CMTD), or peroneal muscular atrophy (PMA), is an uncommon inherited affection of peripheral nerve and probably root, spinal cord, and muscle of young people. Many aspects of the pathology, etiology, and genetics are unresolved and demand a review of previous findings as well as new approaches in future investigations.
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Charcot-Marie-Tooth Disease

2023
Abstract Charcot-Marie-Tooth (CMT) disease is the most common inherited neuromuscular disease and presents many potential considerations for the administration of anesthesia. Type 1 CMT (CMT1) is the most common, of which 70% of cases are CMT1A.
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Charcot—Marie—Tooth disease

1996
The incidence of Charcot—Marie—Tooth disease is undetermined, but it is estimated that around 130 000 Europeans are affected. There are a number of variations of Charcot—Marie—Tooth disease in which deafness and kidney disease are more apparent, and these variations are thought probably to be more common than Charcot—Marie—Tooth without these aspects ...
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Charcot-Marie-Tooth disease.

Journal of manipulative and physiological therapeutics, 1995
To discuss the similarities and differences in the clinical presentation of Charcot-Marie-Tooth Disease, an inherited peripheral neuropathy, and acquired lumbar spinal stenosis.Patients with lumbar spinal stenosis causing nerve root entrapment often have leg pain and weakness during such activities as walking or standing.
J, Martel, D, Mierau, J, Donat
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Bolezen Charcot-Marie-Tooth: Charcot-Marie-Tooth disease:

2003
Background. Charcot-Marie-Tooth (CMT) disease is a common inherited disorder of the peripheral nervous system. In our paper, different types of CMT are described with their typical clinical pictures, electrophysiological signs andmolecular genetic studies. CMT is classified as demyelinative and axonal type and distal motor neuronopathy.
Leonardis, Lea   +2 more
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Periodontal diseases and tooth loss

Periodontology 2000, 1993
R C, Oliver, L J, Brown
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Intermediate Charcot–Marie–Tooth disease: an electrophysiological reappraisal and systematic review

Journal of Neurology, 2017
J. Berciano   +9 more
semanticscholar   +1 more source

Clinical and mutational spectrum of Charcot–Marie–Tooth disease type 2Z caused by MORC2 variants in Japan

European Journal of Neurology, 2017
M. Ando   +15 more
semanticscholar   +1 more source

The role of biomineralization in disorders of skeletal development and tooth formation

Nature Reviews Endocrinology, 2021
Christopher S Kovacs   +2 more
exaly  

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