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Archives de Pediatrie
Volumn 13, Issue 6, 2006, Pages 727-729
Inherited renal diseases and prenatal diagnosis;Néphropathies héréditaires et diagnostic anténatal génétique
Author keywords

Autosomal recessive polycystic kidney disease; Hereditary nephritis; Prenatal diagnosis; Primary hyperoxaluria type 1
Indexed keywords

ALPORT SYNDROME; CYSTINOSIS; HUMAN; INHERITANCE; KIDNEY DISEASE; LETTER; OXALOSIS 1; PRENATAL DIAGNOSIS;
EID: 33646944759     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arcped.2006.03.064     Document Type: Letter
Times cited : (4)
References (9)
  • 1
    • 17944395745 scopus 로고    scopus 로고
    • Apport de la génétique à la connaissance et à la prise en charge des maladies rénales héréditaires progressant vers l'insuffisance rénale
    • Levy M., Gubler M.C., and Feingold J. Apport de la génétique à la connaissance et à la prise en charge des maladies rénales héréditaires progressant vers l'insuffisance rénale. Arch. Pediatr. 8 (2001) 1086-1098
    • (2001) Arch. Pediatr. , vol.8 , pp. 1086-1098
    • Levy, M.1    Gubler, M.C.2    Feingold, J.3
  • 2
    • 0030856752 scopus 로고    scopus 로고
    • Apport de la biologie moléculaire dans le diagnostic des néphropathies héréditaires monogéniques
    • Antignac C. Apport de la biologie moléculaire dans le diagnostic des néphropathies héréditaires monogéniques. Rev. Prat. 47 (1997) 1530-1535
    • (1997) Rev. Prat. , vol.47 , pp. 1530-1535
    • Antignac, C.1
  • 3
    • 2342449228 scopus 로고    scopus 로고
    • Characterization of microsatellite markers to diagnose ADPKD
    • Bae Y., Kim H., Paik M., et al. Characterization of microsatellite markers to diagnose ADPKD. Mol. Cell. Probes 18 (2004) 155-159
    • (2004) Mol. Cell. Probes , vol.18 , pp. 155-159
    • Bae, Y.1    Kim, H.2    Paik, M.3
  • 4
    • 2342544210 scopus 로고    scopus 로고
    • PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease
    • Bergmann C., Senderek J., Schneider F., et al. PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease. Hum. Mutat. 23 (2004) 487-495
    • (2004) Hum. Mutat. , vol.23 , pp. 487-495
    • Bergmann, C.1    Senderek, J.2    Schneider, F.3
  • 6
    • 21244492032 scopus 로고    scopus 로고
    • Primary hyperoxaluria type 1: is genotyping clinically helpful?
    • Leumann E., and Hoppe B. Primary hyperoxaluria type 1: is genotyping clinically helpful?. Pediatr. Nephrol. 20 (2005) 555-557
    • (2005) Pediatr. Nephrol. , vol.20 , pp. 555-557
    • Leumann, E.1    Hoppe, B.2
  • 7
    • 20444469534 scopus 로고    scopus 로고
    • Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family
    • Gigante M., Greco P., Defazio V., et al. Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family. Prenat. Diagn. 25 (2005) 407-410
    • (2005) Prenat. Diagn. , vol.25 , pp. 407-410
    • Gigante, M.1    Greco, P.2    Defazio, V.3
  • 8
    • 0035107123 scopus 로고    scopus 로고
    • Antenatal genetic screening for congenital nephrosis
    • Kallinen J., Heinonen S., Ryynänen M., et al. Antenatal genetic screening for congenital nephrosis. Prenat. Diagn. 21 (2001) 81-84
    • (2001) Prenat. Diagn. , vol.21 , pp. 81-84
    • Kallinen, J.1    Heinonen, S.2    Ryynänen, M.3
  • 9
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    • Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint
    • Pollak M.R. Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint. J. Am. Soc. Nephrol. 13 (2002) 3016-3023
    • (2002) J. Am. Soc. Nephrol. , vol.13 , pp. 3016-3023
    • Pollak, M.R.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.