Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Biol Regul Homeost Agents ; 32(6 Suppl. 1): 157-162, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30644297

RESUMO

Müller-Weiss (MW) disease is a spontaneous osteonecrosis of the tarsal navicular bone in adults. It is a rare cause of chronic medial midfoot pain and deformity characterized by the collapse of the dorso-lateral part of the navicular, progressive navicular fragmentation and talonavicular joint destruction. This study provides a review of the literature about the epidemiology, etio-pathogenesis, clinical, radiological findings and therapeutic alternatives.


Assuntos
Doenças Ósseas , Doenças das Cartilagens , Osteonecrose , Ossos do Tarso/patologia , Humanos
2.
Osteoarthritis Cartilage ; 13(11): 1025-8, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16198603

RESUMO

OBJECTIVES: Osteoarthritis (OA) is considered a polygenic disease controlled by the expression of genetic factors. Genes encoding for cytokines have been associated with susceptibility for joint OA and interleukin (IL)-6 gene is also supposed to be involved in the cartilage degradation process. In this case-control study, we evaluated for the first time whether the risk of hip OA might be influenced by the -174 IL-6 gene polymorphism. METHODS: The distribution of IL-6 genotypes was evaluated in 75 patients affected by hip OA and in 107 age- and sex-matched controls. RESULTS: The distribution of IL-6 genotypes in (1) patients with hip OA: 33 GG, 30 GC, 12 CC and (2) control subjects: 34 GG, 40 GC, 33 CC. The frequency of the CC genotype was significantly higher in control patients (P=0.02). Logistic regression analysis indicated that the presence of the CC genotype is independently associated with a decreased risk of OA (odds ratio 0.4 [95% confidence interval 0.1-0.9], P=0.04). CONCLUSIONS: Primary OA of the hip has an important genetic component and variations of genes encoding for inflammatory cytokines, such as IL-6, may play an important role in the series of events responsible for the pathophysiology of OA.


Assuntos
Interleucina-6/genética , Osteoartrite do Quadril/genética , Polimorfismo Genético/genética , Idoso , Alelos , Estudos de Casos e Controles , Feminino , Frequência do Gene , Genótipo , Humanos , Masculino , Fatores de Risco
3.
Astrophys J ; 525(2): L73-L76, 1999 Nov 10.
Artigo em Inglês | MEDLINE | ID: mdl-10525457

RESUMO

We present results from a BeppoSAX observation of the rich cluster Abell 2319. The broadband spectrum (2-50 keV) of the cluster can be adequately represented by an optically thin thermal emission model with a temperature of 9.6+/-0.3 keV and a metal abundance of 0.25+/-0.03 in solar units and with no evidence of a hard X-ray excess in the PDS spectrum. From the upper limit to the hard-tail component, we derive a lower limit of approximately 0.04 µG for the volume-averaged intracluster magnetic field. By performing spatially resolved spectroscopy in the medium energy band (2-10 keV), we find that the projected radial temperature and metal abundance profiles are constant out to a radius of 16&arcmin; (1.4 Mpc). A reduction of the temperature of one-third, when going from the cluster core out to 16&arcmin;, can be excluded in the present data at the 99% confidence level. From the analysis of the temperature and abundance maps, we find evidence of a temperature enhancement and of an abundance decrement in a region localized 6&arcmin;-8&arcmin; northeast of the core, where a merger event may be taking place. Finally, the temperature map indicates that the subcluster located northwest of the main cluster may be somewhat cooler than the rest of the cluster.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...