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Hereditary multiple exostoses with cervical spine involvement: a case report: Retraction. [PDF]
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New England Journal of Medicine, 1949
HEREDITARY multiple exostoses are a distinct clinical entity more frequently encountered than is generally appreciated. We have recently had the opportunity of studying 4 members of a Negro family who had the condition. Few cases occurring in Negroes are reported in the American literature.1 2 3 To our knowledge this is the first Negro family studied ...
J, ROSE, P D, DOOLAN
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HEREDITARY multiple exostoses are a distinct clinical entity more frequently encountered than is generally appreciated. We have recently had the opportunity of studying 4 members of a Negro family who had the condition. Few cases occurring in Negroes are reported in the American literature.1 2 3 To our knowledge this is the first Negro family studied ...
J, ROSE, P D, DOOLAN
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Radiology, 1952
Hereditary multiple exostoses is a familial disturbance in the growth of cartilaginous bone tissue, most marked at the diaphyso-epiphyseal junction of the long bones. Until the report of Ehrenfried (1) in 1917, mention of this disease was relatively infrequent in the American literature, but since that time numerous cases have been reported (2).
J D, STARK, N N, ADLER, W H, ROBINSON
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Hereditary multiple exostoses is a familial disturbance in the growth of cartilaginous bone tissue, most marked at the diaphyso-epiphyseal junction of the long bones. Until the report of Ehrenfried (1) in 1917, mention of this disease was relatively infrequent in the American literature, but since that time numerous cases have been reported (2).
J D, STARK, N N, ADLER, W H, ROBINSON
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Hereditary Multiple Exostoses with Pseudoaneurysm
CardioVascular and Interventional Radiology, 2007A 16-year-old male patient with hereditary multiple exostoses (HME) was found to have a pseudoaneurysm of the left popliteal artery caused by osteochondroma in the lower femur. The diagnosis was confirmed by ultrasound, magnetic resonance imaging and magnetic resonance angiography without the need to perform an angiogram. The osteochondroma was excised
Azmy M, Al-Hadidy +5 more
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The hip in hereditary multiple exostoses
The Journal of Bone and Joint Surgery. British volume, 2001We defined the characteristics of dysplasia and coxa valga in hereditary multiple exostoses (HME) by radiological analysis of 24 hips in 12 patients. The degree and effect of the ‘osteochondroma load’ around the hip were quantified. We investigated the pathology of the labrum and the incidence of osteoarthritis and of malignant change in these ...
D E, Porter, M K, Benson, G A, Hosney
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Manifestations of Hereditary Multiple Exostoses
Journal of the American Academy of Orthopaedic Surgeons, 2005The solitary osteochondroma, a common pediatric bone tumor, is a cartilage-capped exostosis. Hereditary multiple exostosis is an autosomal dominant disorder manifested by the presence of multiple osteochondromas. Linkage analysis has implicated mutations in the EXT gene family, resulting in an error in the regulation of normal chondrocyte proliferation
Jonathan R, Stieber, John P, Dormans
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Hereditary Multiple Exostoses With Myelopathy
Archives of Neurology, 1979A 58-year-old woman with hereditary multiple exostoses had slowly progressive myelopathy due to a vertebral exostosis that compressed the spinal cord at T1-2. She did not show skeletal deformities, but had numerous palpable long-bone exostoses. While CNS complications are rare in hereditary multiple exostosis, 17 other cases have been reported.
S U, Ho, H L, Lipton
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