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Volumn 34, Issue 1, 1997, Pages 79-82

The cervical spine in Saethre-Chotzen syndrome

Author keywords

cervical spine; craniosynostosis; Saethre Chotzen syndrome

Indexed keywords

ARTICLE; CERVICAL SPINE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; CRANIOFACIAL SYNOSTOSIS; HUMAN; INFANT; MALFORMATION SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; PTOSIS; SCHOOL CHILD; SYNDACTYLY; VERTEBRA MALFORMATION;

EID: 0031053131     PISSN: 10556656     EISSN: None     Source Type: Journal    
DOI: 10.1597/1545-1569(1997)034<0079:TCSISC>2.3.CO;2     Document Type: Article
Times cited : (19)

References (16)
  • 1
    • 0001956946 scopus 로고
    • Eine eigenartige familiare Entwicklungsstoruag. (Arocephalosyndaktylie, Dysosis craniofacialis und hypertelorismus)
    • CHOTZEN F. Eine eigenartige familiare Entwicklungsstoruag. (Arocephalosyndaktylie, Dysosis craniofacialis und hypertelorismus). Monatsschr Kinderheilk 1932;55:97-122.
    • (1932) Monatsschr Kinderheilk , vol.55 , pp. 97-122
    • Chotzen, F.1
  • 3
    • 0023571640 scopus 로고
    • Cervical spine anomalies in the craniosynostosis syndromes
    • HEMMER KM, MCALISTER WH, MARSH JL. Cervical spine anomalies in the craniosynostosis syndromes Cleft Palate J 1987;24:328-333.
    • (1987) Cleft Palate J , vol.24 , pp. 328-333
    • Hemmer, K.M.1    Mcalister, W.H.2    Marsh, J.L.3
  • 4
    • 0019757241 scopus 로고
    • Crouzon syndrome, a clinical and roentgen-cephalometric study
    • KREIBORG S. Crouzon syndrome, a clinical and roentgen-cephalometric study. Scand J Plast Reconstr Surg (Suppl) 1981;18:1-198.
    • (1981) Scand J Plast Reconstr Surg , vol.18 , Issue.SUPPL. , pp. 1-198
    • Kreiborg, S.1
  • 8
    • 0028046606 scopus 로고
    • A common mutation in the fibroblastic growth factor receptor 1 gene in Pfeiffer syndrome
    • MUENKE M, SCHELL U, HEHR A, et al. A common mutation in the fibroblastic growth factor receptor 1 gene in Pfeiffer syndrome. Nat Genet 1994;8:269-274.
    • (1994) Nat Genet , vol.8 , pp. 269-274
    • Muenke, M.1    Schell, U.2    Hehr, A.3
  • 11
    • 0028263955 scopus 로고
    • Saethre-Chotzen syndrome
    • REARDON W, WINTER RM. Saethre-Chotzen syndrome J Med Genet 1994;31:393-396.
    • (1994) J Med Genet , vol.31 , pp. 393-396
    • Reardon, W.1    Winter, R.M.2
  • 12
    • 0001636485 scopus 로고
    • Ein Beitrag zum Turmschaedelproblem. (Pathogenese, Erblichkeit und Symptomologie)
    • SAETHRE H. Ein Beitrag zum Turmschaedelproblem. (Pathogenese, Erblichkeit und Symptomologie). Dtsch Z Nervenheilk 1931;117.533-555.
    • (1931) Dtsch Z Nervenheilk , vol.117 , pp. 533-555
    • Saethre, H.1
  • 13
    • 7144228871 scopus 로고
    • The Saethre-Chotzen syndrome
    • Monasterio FO, ed. Bologna: Monduzzi Editore
    • SHALIN P, LAURITZEN C, JENSEN P. The Saethre-Chotzen syndrome. In: Monasterio FO, ed. Craniofacial surgery. Bologna: Monduzzi Editore, 1994:153-156.
    • (1994) Craniofacial Surgery , pp. 153-156
    • Shalin, P.1    Lauritzen, C.2    Jensen, P.3
  • 14
    • 2442744466 scopus 로고
    • Congenital deformities of the spine; an analysis of the spines of 700 children
    • SHANDS AR, BUNDENS WD. Congenital deformities of the spine; an analysis of the spines of 700 children. Bull Hosp Joint Dis 1956;17:110-133.
    • (1956) Bull Hosp Joint Dis , vol.17 , pp. 110-133
    • Shands, A.R.1    Bundens, W.D.2
  • 16
    • 0028798546 scopus 로고
    • Apert syndrome results from localized mutations of FGFR2 and is alleic with Crouzon syndrome
    • WILKIE AOM, SLANEY SF, OLDRIDGE M, et al. Apert syndrome results from localized mutations of FGFR2 and is alleic with Crouzon syndrome. Nat Genet 1995;9:165-171
    • (1995) Nat Genet , vol.9 , pp. 165-171
    • Wilkie, A.O.M.1    Slaney, S.F.2    Oldridge, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.