Aims. The primary aim of this study was to assess whether the postoperative
Aims. To report mid- to long-term results of
Aims. The main objective of this study was to examine whether the
Aims. Approved by the Food and Drug Administration in 2004, the Phase
III
Aims. The aim of this study was to determine if the
This prospective study describes the outcome of the first 1000 phase 3
We carried out a prospective investigation into
the radiological outcomes of uncemented
Medium-term survivorship of the
This prospective study describes the complications and survival of the first 688 Phase 3
The
The
We have used the
Patellofemoral joint degeneration is often considered a contraindication to medial unicompartmental knee replacement. We examined the validity of this preconception using information gathered prospectively on the intra-operative status of the patellofemoral joint in 824 knees in 793 consecutive patients who underwent
We studied the bone mineral density (BMD) and
the bone mineral content (BMC) of the proximal tibia in patients with
a well-functioning uncemented
We analysed data from the
The
The aim of this study was to evaluate the risk
factors for dislocation of the bearing after a mobile-bearing
The Cementless
The
We developed the