Hemolytic uremic syndrome in three adult siblings: a familial study and evolution.

No abstract is available for this paper.

• Publication year

  1987

• Venue

  Clinical Nephrology

• Publication date

  1987-11-01

• Fields of study

  Medicine

• Identifiers
  PMID 3480783
• 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.

• Familial occurrence of the haemolytic uraemic syndrome.

  2009cited by this paper
• Disturbances of prostacyclin metabolism in children with hemolytic-uremic syndrome and in first degree relatives.

  1986cited by this paper
• Recurrent hemolytic-uremic syndrome with the hypomorphic fast allele of the third component of complement.

  1985cited by this paper
• Partial isolation and function of the prostacyclin regulating plasma factor.

  1985cited by this paper
• Hemolytic uremic syndrome--then and now.

  1985cited by this paper
• Abnormal VIII: von Willebrand factor patterns in the plasma of patients with the hemolytic-uremic syndrome.

  1984cited by this paper
• Deficiency of antithrombin III in children with hemolytic-uremic syndrome

  1984cited by this paper
• Hemolytic uremic syndrome in 3 siblings.

  1984cited by this paper
• Haemolytic uraemic syndrome.

  1984cited by this paper
• Inhibitor of prostacyclin production in sporadic haemolytic uraemic syndrome.

  1983cited by this paper
• Hemolytic uremic syndrome in two postmenopausal women taking a conjugated estrogen preparation.

  1982cited by this paper
• Hereditary thrombotic thrombocytopenic purpura: microangiopathic hemolytic anemia, thrombocytopenia, and renal insufficiency occurring in consecutive generations.

  1982cited by this paper
• Accelerated prostacyclin degradation in the thrombotic thrombocytopenic purpura.

  1981cited by this paper
• Recurrent hemolytic uremic syndrome during oral contraception.

  1981cited by this paper
• Hemolytic-uremic syndrome in two siblings from a nonendemic area.

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• Familial hypocomplementemic hemolytic uremic syndrome with HLA-A3,B7 haplotype.

  1981cited by this paper
• Thrombotic thrombocytopenic purpura and hemolytic-uremic syndrome in HLA-identical siblings.

  1980cited by this paper
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• Prognostic importance of vascular lesions in acute renal failure with microangiopathic hemolytic anemia (hemolytic-uremic syndrome): clinicopathologic study in 20 adults.

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• Hemolytic-uremic syndrome.

  1979cited by this paper
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  1978cited by this paper
• Familial haemolytic uraemic syndrome.

  1978cited by this paper
• Hemolytic-uremic syndrome after shigellosis. Relation to endotoxemia and circulating immune complexes.

  1978cited by this paper
• Adult hemolytic-uremic syndrome. Familial variant.

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  1975cited by this paper
• The haemolytic uraemic syndrome--a family study.

  1975cited by this paper
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  1975cited by this paper
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  1975cited by this paper
• HEMOLYTIC-UREMIC SYNDROME IN ADULT SISTERS

  1974cited by this paper
• Haemolytic uraemic syndrome in women taking oral contraceptives.

  1974cited by this paper

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• Recurrence of HUS Due to CD46/MCP Mutation After Renal Transplantation: A Role for Endothelial Microchimerism

  2007cites this paper
• Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome.

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• Towards a new classification of hemolytic uremic syndrome

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• Membrane Cofactor Protein and Factor I: Mutations and Transplantation

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• Membrane cofactor protein and factor I: mutations and transplantation.

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• COMPLEMENT AND KIDNEY DISEASE

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• Non-Shiga toxin-associated hemolytic uremic syndrome

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• Genetic testing in atypical HUS and the role of membrane cofactor protein (MCP; CD46) and Factor I

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• Mutations in CD46, a complement regulatory protein, predispose to atypical HUS.

  2004cites this paper
• Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.

  2003cites this paper
• The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children

  2003cites this paper
• Familial haemolytic uraemic syndrome and an MCP mutation.

  2003cites this paper
• Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome

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• Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

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• Post-transplant hemolytic-uremic syndrome.

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• Drug-Induced Thrombotic Microangiopathy

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• Hemolytic-Uremic Syndrome and Complement Factor H Deficiency: Clinical Aspects

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• The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.

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• Hemolytic Uremic Syndrome: Recurrence after Renal Transplantation

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• Hemolytic uremic syndrome. Recurrence after renal transplantation. Groupe Coopératif de l'Ile-de-France (GCIF).

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• Familial hemolytic-uremic syndrome in three generations.

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• Renal transplantation in adults with autosomal recessive inheritance of hemolytic uremic syndrome.

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• Adult Group B Streptococcal Disease

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  1995cites this paper
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• A congenital variant of thrombotic thrombocytopenic purpura in two siblings.

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• Inheritance of Glomerular Diseases

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