FP064ASSESSING THE LONG TERM OUTCOMES OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE (ADPKD) USING THE ADPKD OUTCOMES MODEL: A UK CASE STUDY Free

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Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus. Get access

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Correction of metabolic acidosis increases serum albumin concentrations and decreases kinetically evaluated protein intake in haemodialysis patients: a prospective study. Get access

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A large TSC2 and PKD1 gene deletion is associated with renal and extrarenal signs of autosomal dominant polycystic kidney disease. Get access

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Oral-facial-digital syndrome type I: an unusual cause of hereditary cystic kidney disease. Get access

Cholesterol atheromatous embolism: an increasingly recognized cause of acute renal failure Get access

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Inappropriate ADH secretion: an unusual manifestatior of antiphospholipid syndrome? Get access

Antiphospholipid syndrome and glomerular thrombosis in the absence of overt lupus nephritis Get access

Familial occurrence of primary glomerulonephritis: evidence for a role of genetic factors Get access

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Viral Hepatitis in HBsAg-Positive Renal Transplant Patients Treated with Cyclosporin and Steroids Get access

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