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Volumn 24, Issue 2, 2004, Pages 151-153

First-trimester increased nuchal translucency a prenatal sign of Zellweger syndrome [2]

Author keywords

[No Author keywords available]

Indexed keywords

VERY LONG CHAIN FATTY ACID;

EID: 1542351155     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.805     Document Type: Letter
Times cited : (4)

References (13)
  • 2
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    • Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders
    • Brosius U, Gartner J. 2002. Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders. Cell Mol Life Sci 59: 1058-1069.
    • (2002) Cell Mol Life Sci , vol.59 , pp. 1058-1069
    • Brosius, U.1    Gartner, J.2
  • 4
    • 0032997761 scopus 로고    scopus 로고
    • Enlarged nuchal translucency and low serum protein concentrations as possible markers of Zellweger syndrome
    • de Graaf IM, Pajkrt E, Keessen M, Leschot NJ, Bilardo CM. 1999. Enlarged nuchal translucency and low serum protein concentrations as possible markers of Zellweger syndrome. Ultrasound Obstet Gynecol 13: 268-270.
    • (1999) Ultrasound Obstet Gynecol , vol.13 , pp. 268-270
    • De Graaf, I.M.1    Pajkrt, E.2    Keessen, M.3    Leschot, N.J.4    Bilardo, C.M.5
  • 5
    • 0036796075 scopus 로고    scopus 로고
    • Increased nuchal translucency in fetuses with a normal karyotype
    • Hyett JA. 2002. Increased nuchal translucency in fetuses with a normal karyotype. Prenat Diagn 22: 864-868.
    • (2002) Prenat Diagn , vol.22 , pp. 864-868
    • Hyett, J.A.1
  • 6
    • 0035014886 scopus 로고    scopus 로고
    • First-trimester increased nuchal translucency and fetal hypokinesia associated with Zellweger syndrome
    • Johnson JM, Babul-Hirji R, Chitayat D. 2001. First-trimester increased nuchal translucency and fetal hypokinesia associated with Zellweger syndrome. Ultrasound Obstet Gynecol 17: 344-346.
    • (2001) Ultrasound Obstet Gynecol , vol.17 , pp. 344-346
    • Johnson, J.M.1    Babul-Hirji, R.2    Chitayat, D.3
  • 7
    • 0022006985 scopus 로고
    • The cerebrohepatorenal (Zellweger) syndrome: An improved method for the biochemical diagnosis and its potential value for prenatal detection
    • Roscher A, Molzer B, Bernheimer H, Stockler S, Mutz I, Paltauf F. 1985. The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detection. Pediatr Res 19: 930-933.
    • (1985) Pediatr Res , vol.19 , pp. 930-933
    • Roscher, A.1    Molzer, B.2    Bernheimer, H.3    Stockler, S.4    Mutz, I.5    Paltauf, F.6
  • 8
    • 0031926213 scopus 로고    scopus 로고
    • Defects and syndromes in chromosomally normal fetuses with increased nuchal translucency thickness at 10-14 weeks of gestation
    • Souka AP, Snijders RJM, Novakov A, Soares W, Nicolaides KH. 1998. Defects and syndromes in chromosomally normal fetuses with increased nuchal translucency thickness at 10-14 weeks of gestation. Ultrasound Obstet Gynecol 11: 391-400.
    • (1998) Ultrasound Obstet Gynecol , vol.11 , pp. 391-400
    • Souka, A.P.1    Snijders, R.J.M.2    Novakov, A.3    Soares, W.4    Nicolaides, K.H.5
  • 9
    • 0345517153 scopus 로고    scopus 로고
    • Peroxisomal disorders: Clinical and biochemical studies in 15 children and prenatal diagnosis in 7 families
    • Steinberg SJ, Elcioglu N, Slade CM, et al. 1999. Peroxisomal disorders: Clinical and biochemical studies in 15 children and prenatal diagnosis in 7 families. Am J Med Genet 85: 502-510.
    • (1999) Am J Med Genet , vol.85 , pp. 502-510
    • Steinberg, S.J.1    Elcioglu, N.2    Slade, C.M.3
  • 10
    • 0031927893 scopus 로고    scopus 로고
    • Outcome and early childhood follow-up of chromosomally normal fetuses with increased nuchal translucency at 10-14 weeks' gestation
    • Van Vugt JMG, Tinnemans BWS, van Zalen-Sprock RM. 1998. Outcome and early childhood follow-up of chromosomally normal fetuses with increased nuchal translucency at 10-14 weeks' gestation. Ultrasound Obstet Gynecol 11: 407-409.
    • (1998) Ultrasound Obstet Gynecol , vol.11 , pp. 407-409
    • Van Vugt, J.M.G.1    Tinnemans, B.W.S.2    Van Zalen-Sprock, R.M.3
  • 13
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    • Peroxisomale Stoffwechselerkrankungen. Entwicklungsstörungen von Peroxisomen
    • Weller S, Gartner J. 2002. Peroxisomale Stoffwechselerkrankungen. Entwicklungsstörungen von Peroxisomen. Monatsschr Kinderheilkd 150: 226-237.
    • (2002) Monatsschr Kinderheilkd , vol.150 , pp. 226-237
    • Weller, S.1    Gartner, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.