Hyperfiltration and renal disease in glycogen storage disease, type I.

No abstract is available for this paper.

• Publication year

  1989

• Venue

  Kidney International

• Publication date

  1989-06-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1038/KI.1989.133PMID 2671467
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• The Glycogen-Storage Diseases

  1990cited by this paper
• Progression of renal disease.

  1989cited by this paper
• The progression of renal disease.

  1989cited by this paper
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  1988cited by this paper
• Renal disease in type I glycogen storage disease.

  1988cited by this paper
• Renal glomerular and tubular abnormalities in glycogen storage disease type I.

  1988cited by this paper
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  1984cited by this paper
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  1984cited by this paper
• Sonographic assessment of renal length in normal children.

  1984cited by this paper
• Enzyme immunoassay for urinary albumin.

  1983cited by this paper
• The Stages in Diabetic Renal Disease: With Emphasis on the Stage of Incipient Diabetic Nephropathy

  1983cited by this paper
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  1982cited by this paper
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  1982cited by this paper
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  1981cited by this paper
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  1967cited by this paper
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