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osteogenesis imperfecta
Abnormally low values were seen in all untreated children with idiopathic juvenile osteoporosis, 3/9 steroid recipients, and three patients with osteogenesis imperfecta.
      
Osteogenesis imperfecta complicated by osteosarcoma
      
Percutaneous vertebroplasty in the treatment of vertebral body compression fracture secondary to osteogenesis imperfecta
      
We present a case and extend the indication of percutaneous vertebroplasty in a patient with a vertebral body compression fracture secondary to osteogenesis imperfecta.
      
Percutaneous vertebroplasty in the treatment of vertebral body compression fracture secondary to osteogenesis imperfecta
      
Pseudomass of the sternal manubrium in osteogenesis imperfecta
      
Hyperplastic callus formation in osteogenesis imperfecta type V mimicking osteosarcoma: 4-year follow-up with resolution
      
We report a case of hyperplastic callus formation that occurred in both femurs in a patient with type V osteogenesis imperfecta (OI), with 4-year follow-up and resolution.
      
Hyperplastic callus formation in osteogenesis imperfecta type?V: follow-up of three generations over ten years
      
Hyperplastic callus (HPC) formation is a prominent feature of osteogenesis imperfecta (OI) type?V; however, little is known about its long-term outcome.
      
Percutaneous nailing in the management of osteogenesis imperfecta
      
Marked deformities of the skeleton may develop in the severe form of osteogenesis imperfecta.
      
Eight years ago, axial correction of deformities of the femora and tibiae by manual osteoclasis was carried out in a 7 year old girl in whom osteogenesis imperfecta had produced severe bowing of the long bones of the legs.
      
Fractures of the proximal femur frequently occur in children with osteogenesis imperfecta or fibrous dyplasia and may lead to progressive coxa vara and a "shepherds crook" deformity.
      
The purpose of this study was to quantify the physical and mental health of a diverse adult cohort of patients with osteogenesis imperfecta (OI) utilizing a validated health self-assessment questionnaire (SF-36).
      
In addition, a specific demographic questionnaire and a functional questionnaire were utilized to assess more specifically the physical limitations imposed by osteogenesis imperfecta in adulthood.
      
Osteosarcoma occurring in osteogenesis imperfecta tarda
      
The combination of osteogenesis imperfecta (OI) and osteosarcoma is rare, as reflected by the fact that there are only eight proven cases in the published English literature.
      
Two older boys were diagnosed as osteogenesis imperfecta.
      
This syndrome radiologically simulates osteogenesis imperfecta.
      
 

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