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Volumn 27, Issue 18, 2002, Pages 1995-2002

Spinal deformity in chondrodysplasia punctata

Author keywords

Cervical spine dysplasia; Chondrodysplasia punctata; Congenital kyphoscoliosis; Conradi Huenermann syndrome

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHONDRODYSPLASIA PUNCTATA; CLINICAL ARTICLE; DISEASE COURSE; DYSPLASIA; EPIPHYSIS DISEASE; FEMALE; HUMAN; KYPHOSCOLIOSIS; KYPHOSIS; MALE; OSTEOTOMY; PRIORITY JOURNAL; PSEUDARTHROSIS; SCOLIOSIS; SHORT STATURE; SPINE FUSION; SPINE MALFORMATION; SPINE RADIOGRAPHY; SURGICAL TECHNIQUE; VERTEBRA BODY;

EID: 0037106126     PISSN: 03622436     EISSN: None     Source Type: Journal    
DOI: 10.1097/00007632-200209150-00007     Document Type: Article
Times cited : (35)

References (14)
  • 1
    • 0015295169 scopus 로고
    • Atlanto-axial dislocation in chondrodysplasia punctata: Report of the findings in two brothers
    • (1972) Radiology , vol.102 , pp. 399-401
    • Afshani, E.1    Girdany, B.R.2
  • 11
    • 0033624130 scopus 로고    scopus 로고
    • The Conradi-Hunermann-Happle syndrome is caused by mutations in the gene that encodes a 8-7 sterol isomerase and is biochemically related to the CHILD syndrome
    • (2000) Eur J Dermatol , vol.10 , pp. 425-428
    • Traupe, H.1    Has, C.2
  • 12
    • 0031903775 scopus 로고    scopus 로고
    • Cholesterol biosynthesis, peroxisomes and peroxisomal disorders: Mevalonate kinase is not only deficient in Zellweger syndrome but also in rhizomelic chondrodysplasia punctata
    • (1998) J Inherit Metab Dis , vol.21 , pp. 309-312
    • Wanders, R.J.1    Romeijn, G.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.