Zobrazeno 1 - 10
of 34
pro vyhledávání: '"M. D. Fallon"'
Publikováno v:
Clinical orthopaedics and related research. (294)
Spinal bone density was measured in eight patients with osteopetrosis to assess the natural history of the disease and to monitor the response to therapy. Quantitative computed tomographic scans of the lumbar vertebra were obtained in seven patients,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::033b922cb72242d7cd54d21e43beb039
https://pubmed.ncbi.nlm.nih.gov/8358948
https://pubmed.ncbi.nlm.nih.gov/8358948
Publikováno v:
Clinical orthopaedics and related research. (294)
Rickets is a common and paradoxical feature of infantile malignant osteopetrosis and results from the inability of osteoclasts to maintain a normal calcium-phosphorus balance in the extracellular fluid. Despite a markedly positive total body calcium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2afd1afe54353b0cc53bd4776334e52
https://pubmed.ncbi.nlm.nih.gov/8395371
https://pubmed.ncbi.nlm.nih.gov/8395371
Publikováno v:
Clinical orthopaedics and related research. (294)
Fibrodysplasia ossificans progressiva (FOP) is a rare heritable disorder characterized by progressive heterotopic endochondral bone formation arising in ligament, tendon, and the fibrous connective tissue of skeletal muscle. The disorder is almost in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c8e18825fb69fbcdeb31ecdba2e0b587
https://pubmed.ncbi.nlm.nih.gov/8358928
https://pubmed.ncbi.nlm.nih.gov/8358928
Publikováno v:
Clinical orthopaedics and related research. (293)
Osteogenesis imperfecta (OI) Type II is a rare heritable disorder of bone matrix that results in catastrophic congenital skeletal dysplasia. Two cases of OI Type II had symmetric rhizomelic skeletal dysplasia apparent on ultrasound at 16 and 20 weeks
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::47ed53fd98f4f72a0d894a38201da391
https://pubmed.ncbi.nlm.nih.gov/8339500
https://pubmed.ncbi.nlm.nih.gov/8339500
Publikováno v:
Cancer. 71(10)
The combination of a primary osteosarcoma of bone with a second carcinomatous cell type has been recognized, although immunohistochemical studies currently have not been performed in an attempt to understand the histogenesis of such a tumor.In this r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd4528457fe593286772c51d6b02c9d7
https://pubmed.ncbi.nlm.nih.gov/7683966
https://pubmed.ncbi.nlm.nih.gov/7683966
Publikováno v:
Clinical orthopaedics and related research. (285)
Disorders of joints are commonly associated with Paget's disease of bone but are often disregarded or attributed to the underlying Pagetic condition. The authors evaluated a 69-year-old man with extensive Paget's disease of bone, degenerative arthrit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ea838525249554bdc82949b4a0d4fd1e
https://pubmed.ncbi.nlm.nih.gov/1446446
https://pubmed.ncbi.nlm.nih.gov/1446446
Publikováno v:
Clinical orthopaedics and related research. (280)
Estrogen has profound effects on the regulation of bone metabolism, but its role in fracture healing is unknown. Several recent reports have documented the presence of estrogen receptors in vitro and in diseased tissue. The authors investigated estro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e1e487084eacdd6602bc2216be4f0620
https://pubmed.ncbi.nlm.nih.gov/1611758
https://pubmed.ncbi.nlm.nih.gov/1611758
Publikováno v:
Transplantation. 52(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::968187925cd002a5149bbdbd1da8e073
https://pubmed.ncbi.nlm.nih.gov/1716801
https://pubmed.ncbi.nlm.nih.gov/1716801
Publikováno v:
Clinical orthopaedics and related research. (269)
Hurler syndrome is a mucopolysaccharide disorder resulting from an heritable deficiency in alpha-L-iduronidase, an enzyme required in the catabolism of heparan sulfate and dermatan sulfate glycosaminoglycan (GAGs). The resultant intracellular accumul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::537ce0b3b80b1f66b873ba4846e5ea50
https://pubmed.ncbi.nlm.nih.gov/1907534
https://pubmed.ncbi.nlm.nih.gov/1907534
Publikováno v:
Clinical orthopaedics and related research. (250)
Regional migratory osteoporosis (RMO) is an idiopathic disorder characterized by bouts of severe periarticular lower limb pain associated with rapidly developing localized osteoporosis. Symptoms often reverse spontaneously after six to nine months. R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd4de356280d33052e1595b51fd24a2d
https://pubmed.ncbi.nlm.nih.gov/2403495
https://pubmed.ncbi.nlm.nih.gov/2403495