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Volumn 92, Issue 2, 2002, Pages 449-451

Methylenetetrahydrofolate reductase polymorphism in childhood primary focal segmental glomerulosclerosis

Author keywords

Children; Focal segmental glomerulosclerosis; Methylenetetrahydrofolate reductase; Polymorphism

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); HOMOCYSTEINE;

EID: 0036420518     PISSN: 00282766     EISSN: None     Source Type: Journal    
DOI: 10.1159/000063283     Document Type: Article
Times cited : (2)

References (8)
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    • (1994) Pediatric Nephrology , pp. 767-787
    • Barratt, T.M.1    Clark, G.2
  • 3
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    • Miner, S.E.1    Evrovski, J.2    Cole, D.E.3
  • 6
    • 0032497143 scopus 로고    scopus 로고
    • Methylenetetrahydrofolate reductase gene polymorphism as a risk factor for diabetic nephropathy in NIDDM patients
    • Neugebauer S, Baba T, Watanabe T: Methylenetetrahydrofolate reductase gene polymorphism as a risk factor for diabetic nephropathy in NIDDM patients. Lancet 1998;352:454.
    • (1998) Lancet , vol.352 , pp. 454
    • Neugebauer, S.1    Baba, T.2    Watanabe, T.3
  • 7
    • 0342545889 scopus 로고    scopus 로고
    • MTHFR gene polymorphism as an exacerbation factor of diabetic nephropathy in type 2 diabetes: Analysis in Japanese male hemodialysis patients
    • Noiri E, Taguchi J, Nakao A, Fujita T: MTHFR gene polymorphism as an exacerbation factor of diabetic nephropathy in type 2 diabetes: Analysis in Japanese male hemodialysis patients. Diab Care 2000;23:260.
    • (2000) Diab Care , vol.23 , pp. 260
    • Noiri, E.1    Taguchi, J.2    Nakao, A.3    Fujita, T.4
  • 8
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    • The C677T methylenetetrahydrofolate reductase gene mutation in hemodialysis patients
    • Kimura H, Gejyo F, Suzuki S, Miyazaki R: The C677T methylenetetrahydrofolate reductase gene mutation in hemodialysis patients. J Am Soc Nephrol 2000;11:885-893.
    • (2000) J Am Soc Nephrol , vol.11 , pp. 885-893
    • Kimura, H.1    Gejyo, F.2    Suzuki, S.3    Miyazaki, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.