Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Pere Benito Ruiz"'
Autor:
Pere Benito-Ruiz
Publikováno v:
Seminarios de la Fundación Española de Reumatología. 13:3-8
Resumen La artrosis no puede ser considerada como una unica enfermedad, sino como un grupo heterogeneo de patologias con manifestaciones clinicas similares, y cambios patologicos y radiologicos comunes que dificultan el establecimiento de recomendaci
Autor:
L. Pérez-Edo, Sergi Serrano, Jordi Carbonell-Abelló, M. L. Mariñoso, Pere Benito-Ruiz, Josep Blanch-Rubió, Manuel Ciria-Recasens
Publikováno v:
Bone. 36:926-930
Osteoporosis is associated with increased bone resorption together with a decrease in bone formation. In women, there is an increase of resorption surfaces and in the number of osteoclasts. These changes, however, are not found in males. This purpose
Autor:
Pere Benito-Ruiz
Publikováno v:
Reumatología Clínica. 2:S21-S23
Autor:
Pere, Benito-Ruiz
Publikováno v:
Reumatologia clinica. 2
Autor:
Estibaliz, Loza, Pere, Benito-Ruiz, Francisco, Blanco, Eugenio, de Miguel, Jose A, Román, Jose SanAnton, Esquer
Publikováno v:
Clinical and experimental rheumatology. 29(6)
To examine the feasibility and efficacy of a multidisciplinary health care programme for patients with knee OA.A 12-month follow-up care programme for knee OA, based on clinical evidence and expert opinion was implemented in primary care settings. It
Autor:
Joan Garcia, Pere Benito Ruiz, M. Monleón Pradas, José Luis Gómez Ribelles, Enric Cáceres Palou, Natalia Garcia-Giralt, Marcos Pérez Olmedilla
Publikováno v:
Biomaterials. 27(7)
A series of polymer and copolymer networks with varying hydrophilicity and distribution of the hydrophilic groups was synthesized and biologically tested with monolayer culture of human chondrocytes in vitro. Cell viability (MTT), proliferation (BrdU
Abnormal bone scintigraphy and silent radiography in localized reflex sympathetic dystrophy syndrome
Autor:
Emili Martínez-Miralles, Alfons Cuartero-Plaza, Silvia Martínez-Pardo, Manuel P. Sanz Marín, Pere Benito-Ruiz
Publikováno v:
European journal of nuclear medicine. 19(5)
Typical, definite forms of the reflex sympathetic dystrophy syndrome present no diagnostic problems, but the diagnosis of localized or very localized forms is very difficult. In the absence of characteristic roentgenographic evidence of acute, patchy