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Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defects.
Yang, Lin; Liu, Bo; Dong, Xinran; Wu, Jing; Sun, Chengjun; Xi, Li; Cheng, Ruoqian; Wu, Bingbing; Wang, Huijun; Tong, Shiyuan; Wang, Dahui; Luo, Feihong.
Afiliação
  • Yang L; Department of Pediatric Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, 399 Wan Yuan Road, Shanghai, 201102, China.
  • Liu B; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, 201102, China.
  • Dong X; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, 201102, China.
  • Wu J; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, 201102, China.
  • Sun C; Department of Pediatric Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, 399 Wan Yuan Road, Shanghai, 201102, China.
  • Xi L; Department of Pediatric Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, 399 Wan Yuan Road, Shanghai, 201102, China.
  • Cheng R; Department of Pediatric Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, 399 Wan Yuan Road, Shanghai, 201102, China.
  • Wu B; Department of Pediatric Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, 399 Wan Yuan Road, Shanghai, 201102, China.
  • Wang H; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, 201102, China.
  • Tong S; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, 201102, China.
  • Wang D; State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai, 201102, China.
  • Luo F; Division of Orthopedics, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China. wangdahui@fudan.edu.cn.
Osteoporos Int ; 33(6): 1373-1384, 2022 Jun.
Article em En | MEDLINE | ID: mdl-35044492
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese Imperfeita / Colágeno Tipo I / Cadeia alfa 1 do Colágeno Tipo I Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Osteoporos Int Assunto da revista: METABOLISMO / ORTOPEDIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese Imperfeita / Colágeno Tipo I / Cadeia alfa 1 do Colágeno Tipo I Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Osteoporos Int Assunto da revista: METABOLISMO / ORTOPEDIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China