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Camurati‐Engelmann disease type II: Progressive diaphyseal dysplasia with striations of the bones
Authors:Hitoshi Nishimura  Yoko Tanaka  Yoshio Makita  Shiro Ikegawa  Mohsen Ghadami  Akira Kinoshita  Norio Niikawa
Affiliation:1. Department of Orthopedic Surgery, Ishikawa Pediatric Orthopedic Center, Kanazawa, Japan;2. Department of Pediatrics, Ichikawa General Hospital, Tokyo Dental College, Ichikawa, Japan;3. Department of Pediatrics, Asahikawa Medical College, Asahikawa, Japan;4. Department of Public Health, Asahikawa Medical College, Asahikawa, Japan;5. Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN (The Institute of Physical and Chemical Research), Tokyo, Japan;6. Laboratory of Genome Medicine, Institute of Medical Science, Human Genome Center, The University of Tokyo, Tokyo, Japan;7. Department of Human Genetics, Nagasaki University School of Medicine, Nagasaki, Japan
Abstract:
Keywords:hyperostosis generalisata with striations of the bones  progressive diaphyseal dysplasia  Camurati‐Engelmann disease  transforming growth factor beta‐1
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