Results 251 to 260 of about 13,337 (295)
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Solitary Epiphyseal Enchondromas
The Journal of Bone and Joint Surgery (American), 2005Enchondromas originating in the epiphyses of long bones are rare. The purpose of the present study was to evaluate the prevalence as well as the radiographic and clinical characteristics of epiphyseal enchondromas among patients who had been referred to the Armed Forces Institute of Pathology and Walter Reed Army Medical Center.We performed a ...
Benjamin K, Potter +5 more
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Clinical Orthopaedics and Related Research, 1989
Hemichondrodiatasis is a technique of closed, gradual, asymmetric distraction of the growth plate to correct angular deformities in growing children. This report describes the technique and the results achieved in 35 operated lower extremity segments, 14 involving the femur and 21 involving the tibia.
ALDEGHERI, ROBERTO +2 more
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Hemichondrodiatasis is a technique of closed, gradual, asymmetric distraction of the growth plate to correct angular deformities in growing children. This report describes the technique and the results achieved in 35 operated lower extremity segments, 14 involving the femur and 21 involving the tibia.
ALDEGHERI, ROBERTO +2 more
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EPIPHYSEAL CHONDROBLASTOMA OF BONE
The Journal of Bone & Joint Surgery, 1951Epiphyseal chondroblastomata ate tumors of bone, occurring in the adolescent or early adult age group, involving the epiphyses of bones. The origin of this tumor is considered to be a reticulohistiocytic cell which differentiates into chondroblasts and then into cartilage. In the eight cases of this tumor reported, conservative therapy was curative in
J, VALLS, C E, OTTOLENGHI, F, SCHAJOWICZ
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Journal of the American Academy of Orthopaedic Surgeons, 2015
Multiple epiphyseal dysplasia is a genotypically and phenotypically heterogeneous disorder affecting the epiphysis of long bones. Inheritance may be autosomal dominant or autosomal recessive. Autosomal dominant variants include mutations of the collagen oligomeric matrix protein, collagen type IX α-1, collagen type IX α-2, collagen type IX α-3, and ...
Steven, Anthony +3 more
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Multiple epiphyseal dysplasia is a genotypically and phenotypically heterogeneous disorder affecting the epiphysis of long bones. Inheritance may be autosomal dominant or autosomal recessive. Autosomal dominant variants include mutations of the collagen oligomeric matrix protein, collagen type IX α-1, collagen type IX α-2, collagen type IX α-3, and ...
Steven, Anthony +3 more
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Clinical Orthopaedics and Related Research, 1976
The epiphyseal dysplasias are a group of heterogeneous disorders characterized by defective or excessive bone formation in the secondary ossification centers of the tubular bones and sometimes the vertebrae. Most of them are caused by the defective action of mutant genes. Their pathogenesis is unknown.
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The epiphyseal dysplasias are a group of heterogeneous disorders characterized by defective or excessive bone formation in the secondary ossification centers of the tubular bones and sometimes the vertebrae. Most of them are caused by the defective action of mutant genes. Their pathogenesis is unknown.
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The Physician and Sportsmedicine, 1982
In brief In this evaluation of 203 acute epiphyseal fractures in the long bones of 183 patients aged 3 to 18, 79 fractures (39%) were related to the following ten sports activities: football, hockey, basketball, downhill skiing, baseball/softball, wrestling, soccer, gymnastics, tennis, and volleyball.
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In brief In this evaluation of 203 acute epiphyseal fractures in the long bones of 183 patients aged 3 to 18, 79 fractures (39%) were related to the following ten sports activities: football, hockey, basketball, downhill skiing, baseball/softball, wrestling, soccer, gymnastics, tennis, and volleyball.
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The Indian Journal of Pediatrics, 1978
Two families involving 8 members out of a total of 15, studied in more than two generations showing association of interesting radiological and ocular findings, is reported.
V M, Soodan, V, Mohan, S P, Padha
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Two families involving 8 members out of a total of 15, studied in more than two generations showing association of interesting radiological and ocular findings, is reported.
V M, Soodan, V, Mohan, S P, Padha
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1997
Abstract The physis is weaker than the ligaments and so is liable to injury. Beware missing a type V injury, as it may lead to deformity with growth. These are sometimes described as fractures and some¬ times as fracture dislocations.
G R Wilson +3 more
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Abstract The physis is weaker than the ligaments and so is liable to injury. Beware missing a type V injury, as it may lead to deformity with growth. These are sometimes described as fractures and some¬ times as fracture dislocations.
G R Wilson +3 more
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Epiphyseal stippling in acrodysostosis
American Journal of Medical Genetics, 1991AbstractWidespread epiphyseal stippling was demonstrated radiologically during the early months of life in 7 children with acrodysostosis. This finding, which does not seem to have been previously documented in this disorder, is important in the differential diagnosis.
D, Viljoen, P, Beighton
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Disorders of Epiphyses and Metaphyses with Predominant Epiphyseal Involvement
1982The most important disorders in this category are achondroplasia, hypochondroplasia and the metaphyseal dysplasias. The spine and epiphyses may be involved to some degree in each, but metaphyseal changes predominate.
Frank Horan, Peter Beighton
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