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Volumn 23, Issue 1, 2003, Pages 48-51

Congenital nephropathy and ventriculomegaly: A report of four cases

Author keywords

Alpha fetoprotein; Congenital; Nephropathy; Ventriculomegaly

Indexed keywords

ALPHA FETOPROTEIN; DNA;

EID: 12244254689     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.447     Document Type: Article
Times cited : (4)

References (8)
  • 1
    • 0033933128 scopus 로고    scopus 로고
    • Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type
    • Aya K, Tanaka H, Seino Y. 2000. Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type. Kidney Int 57: 401-404.
    • (2000) Kidney Int , vol.57 , pp. 401-404
    • Aya, K.1    Tanaka, H.2    Seino, Y.3
  • 2
    • 0035038042 scopus 로고    scopus 로고
    • Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome
    • Beltcheva O, Maritn P, Lenkkeri U, Tryggvason K. 2001. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome. Hum Mutat 17: 368-373.
    • (2001) Hum Mutat , vol.17 , pp. 368-373
    • Beltcheva, O.1    Maritn, P.2    Lenkkeri, U.3    Tryggvason, K.4
  • 3
    • 0030929381 scopus 로고    scopus 로고
    • Risks for fetal abnormalities after very and moderately elevated AF-AFPs
    • Crandall BF, Chua C. 1997. Risks for fetal abnormalities after very and moderately elevated AF-AFPs. Prenat Diagn 17: 837-841.
    • (1997) Prenat Diagn , vol.17 , pp. 837-841
    • Crandall, B.F.1    Chua, C.2
  • 4
    • 0344541695 scopus 로고    scopus 로고
    • Nephrin localizes at the podocyte filtration slit area and is characteristically spliced in the human kidney
    • Holthofer H, Ahola H. Solin ML, et al. 1999. Nephrin localizes at the podocyte filtration slit area and is characteristically spliced in the human kidney. Am J Pathol 155: 1681-1687.
    • (1999) Am J Pathol , vol.155 , pp. 1681-1687
    • Holthofer, H.1    Ahola, H.2    Solin, M.L.3
  • 5
    • 0017655263 scopus 로고
    • Defect of cerebellar Purkinje cell histogenesis associated with type I and type II renal cystic disease
    • Kornguth S, Knobeloch L, Viseskul C, Gilbert E. Opitz J. 1977. Defect of cerebellar Purkinje cell histogenesis associated with type I and type II renal cystic disease. Acta Neuropathol (Berl) 40: 1-9.
    • (1977) Acta Neuropathol (Berl) , vol.40 , pp. 1-9
    • Kornguth, S.1    Knobeloch, L.2    Viseskul, C.3    Gilbert, E.4    Opitz, J.5
  • 6
    • 0030892236 scopus 로고    scopus 로고
    • Cost-effectiveness of strategies used in the evaluation of pregnancies complicated by elevated maternal serum alpha-fetoprotein levels
    • Nadel AS, Norton ME, Wilkins-Haug L. 1997. Cost-effectiveness of strategies used in the evaluation of pregnancies complicated by elevated maternal serum alpha-fetoprotein levels. Obstet Gynecol 89(5 Pt 1): 660-665.
    • (1997) Obstet Gynecol , vol.89 , Issue.5 PART 1 , pp. 660-665
    • Nadel, A.S.1    Norton, M.E.2    Wilkins-Haug, L.3
  • 7
    • 0024420345 scopus 로고
    • Prenatal diagnosis of cystic kidney disease with ventriculomegaly: A report of six cases in two related sibships
    • Reuss A, den Hollander JC, Niermeijer MF, et al. 1989. Prenatal diagnosis of cystic kidney disease with ventriculomegaly: a report of six cases in two related sibships. Am J Med Genet 33: 385-389.
    • (1989) Am J Med Genet , vol.33 , pp. 385-389
    • Reuss, A.1    Den Hollander, J.C.2    Niermeijer, M.F.3
  • 8
    • 0019028282 scopus 로고
    • Increased amniotic fluid alpha-fetoprotein, familial hydrocephalus, and renal dysmorphology
    • Sinclair-Smith CC, Wiggelinkhuizen J, Nelson MM. 1980. Increased amniotic fluid alpha-fetoprotein, familial hydrocephalus, and renal dysmorphology. Am J Dis Child 134; 619-621.
    • (1980) Am J Dis Child , vol.134 , pp. 619-621
    • Sinclair-Smith, C.C.1    Wiggelinkhuizen, J.2    Nelson, M.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.