Results 301 to 310 of about 9,361,467 (352)

Tooth extraction in patients with heart disease [PDF]

open access: possibleBritish Dental Journal, 1991
A combination of fear and declining compensation may induce cardiovascular accidents in the elderly with heart disease. An accurate cardiac diagnosis and relief of stress and pain during tooth extraction are important. The range of cardiac abnormalities and the regime followed in two clinics in the People's Republic of China are reviewed, together with
Z X Lim, W G Geng
openaire   +2 more sources
Some of the next articles are maybe not open access.

Related searches:

Charcot-Marie-Tooth Disease

Archives of Neurology, 2001
I n 1886, Jean-Martin Charcot and Pierre Marie 1,2 and Henry Tooth independently described the hereditary motor and sensory neuropathy that now bears their names. Their precise clinical description provided the foundation on which later physiological and genetic understanding of hereditary neuropathies is based.
openaire   +2 more sources

Charcot-Marie-Tooth Disease and Vincristine

Journal of the American Podiatric Medical Association, 2003
This article reports on a case of sensorimotor neuropathy in a 55-year-old man that developed after vincristine therapy. Subsequent biopsy of the sural nerve and electromyographic studies revealed the presence of Charcot-Marie-Tooth disease. Only 17 patients who developed severe neuropathy with very low accumulated doses of vincristine have been ...
Javier Pascual-Huerta   +2 more
openaire   +3 more sources

Pathophysiology of Charcot-Marie-Tooth Disease

Clinical Orthopaedics and Related Research, 1988
The etiology of the foot deformity in patients with Charcot-Marie-Tooth disease has not previously been discussed in relation to the extrinsic muscle function around the foot and ankle. Eight adult patients with a strong familial history were evaluated, and their foot findings were remarkably similar.
Roger A. Mann, John Missirian
openaire   +3 more sources

Charcot-Marie-Tooth Disease

JAMA: The Journal of the American Medical Association, 1974
To the Editor.— Charcot-Marie-Tooth disease has traditionally been regarded as a pure neuropathic disease, and Siegel (228:873, 1974) suggested that the myopathic changes in two brothers with this disease could be caused by the neuropathy, in accordance with the "neurogenic hypothesis" of muscle disease.
openaire   +3 more sources

Surgical treatment of cavus foot in Charcot-Marie-tooth disease: a review of twenty-four cases: AAOS exhibit selection.

Journal of Bone and Joint Surgery. American volume, 2015
Charcot-Marie-Tooth disease is the single most common diagnosis associated with cavus foot. The imbalance involving intrinsic and extrinsic muscles has been suggested as the main pathogenetic cause of cavus foot in this disease.
C. Faldini   +7 more
semanticscholar   +1 more source

Axonal Charcot–Marie–Tooth disease

Current Opinion in Neurology, 2011
The aim is to specify the genetic causes of dominantly and recessively inherited axonal forms of Charcot-Marie-Tooth disease (CMT) and review the biological basis for these disorders.More than 10 genes that cause axonal CMT have been identified over the past decade. Many of these genes express proteins that are ubiquitously expressed.
Agnes Patzko, Michael E. Shy
openaire   +2 more sources

Tooth Loss and Alzheimer’s Disease

Current Oral Health Reports, 2019
Alzheimer’s disease (AD) is a major subtype of dementia. Recent cohort studies have demonstrated that loss of masticatory function, periodontitis, and/or tooth loss are risk factors for AD. The present review provides an overview of the existing literature as well as recent evidence regarding the relationship between tooth loss and the onset of AD.
Tetsuya Goto, W. Keung Leung
openaire   +2 more sources

The Hand in Charcot-Marie-Tooth Disease

Journal of Hand Surgery, 1991
The upper extremity was evaluated in 68 symptomatic individuals previously diagnosed as having Charcot-Marie-Tooth disease. Consistent patterns of motor and sensory involvement were found noted as well as a predictable progression of neuromuscular deficits.
L. L. Williams   +3 more
openaire   +3 more sources

Charcot-Marie-Tooth disease type 2A: from typical to rare phenotypic and genotypic features.

JAMA Neurology, 2014
IMPORTANCE Axonal Charcot-Marie-Tooth disease (CMT) is genetically heterogeneous, with 11 genes identified. Axonal CMT has most frequently been associated with mutations in the MFN2 gene (CMT2A).
F. Bombelli   +11 more
semanticscholar   +1 more source

Home - About - Disclaimer - Privacy