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osteogenesis imperfecta
Skin fibroblasts were cultured from 13 patients with Osteogenesis imperfecta and collagen biosynthesis was investigated in vitro.
      
By contrast, fibroblasts obtained from patients with Osteogenesis imperfecta of a more severe type synthesised collagen types I/III in a normal ratio.
      
Diese Frage ist relevant, da viele Patienten, die mit Bisphosphonate wegen Osteoporose, Morbus Paget, Knochentumor oder Osteogenesis imperfecta behandelt werden, eine Fraktur erleiden.
      
Die umfangreichsten Erfahrungen bestehen in der i.v.-Therapie schwerer Verlaufsformen der Osteogenesis imperfecta (OI).
      
Diagnostik und Therapie der Osteogenesis imperfecta
      
Die Osteogenesis imperfecta (OI) ist eine angeborene Erkrankung des Bindegewebes mit einer H?ufigkeit bis zu 1/30.000.
      
Diagnostik und Therapie der Osteogenesis imperfecta
      
In regard to a case of osteogenesis imperfecta tarda the authors pose the problem of the connexion between basilar impression and disorders of mineralization.
      
We report a case of osteosarcoma arising in osteogenesis imperfecta.
      
In addition, the hook may be seen in acquired upper extremity weakness such as in persistent brachial plexus injury after birth trauma and in severe osteogenesis imperfecta.
      
The clinical and radiographic features of 47 cases of neonatally manifest osteogenesis imperfecta were analyzed.
      
Striking similarities with established genetic disorders of collagen (like the osteogenesis imperfecta group and the Ehlers-Danlos syndrome) suggest, however, that the OPS could be a primary collagen disorder.
      
Basilar impression and osteogenesis imperfecta in a three-year-old girl: CT and MRI
      
A 3-year-old girl with osteogenesis imperfecta developed symptomatic basilar impression.
      
Osteoporosis as in myelodysplasia, osteogenesis imperfecta and from other causes was responsible for 52% of insufficiency fractures.
      
Fracture non-union in children and adolescents is often due to an underlying cause such as affliction with neurofibromatosis or osteogenesis imperfecta.
      
The most common disorders diagnosed were osteogenesis imperfecta (OI), thanatophoric dysplasia, campomelic dysplasia and achondrogenesis type II.
      
Craniocervical abnormalities in osteogenesis imperfecta: Genetic and molecular correlation
      
Basilar impression (BI) assessed by either plain lateral skull radiograph or computerized tomography (CT) sagittal reconstruction of the craniocervical junction is a common finding occurring in 25% of subjects with osteogenesis imperfecta (OI).
      
This article reviews some of the other differential diagnoses, particularly osteogenesis imperfecta and the alleged "temporary brittle bone disease".
      
 

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