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Identification of two novel mutations in the CLCN5 gene in Japanese patients with familial idiopathic low molecular weight proteinuria (Japanese Dent's disease)
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EXPERIMENTAL NEPHROLOGY
Isolation and characterization of the human CLC-5 chloride channel gene promoter
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Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis
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Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria
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Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases
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SDS-electrophoresis of unconcentrated urine samples using a semi-automaaicmethod
RENAL FAILURE
RENAL TUBULAR FUNCTION IN BETA-THALASSEMIA
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FUNCTIONAL-CHARACTERIZATION OF RENAL CHLORIDE CHANNEL, CLCN5, MUTATIONS ASSOCIATED WITH DENTS(JAPAN)-DISEASE
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CLCN5 MUTATION SER244LEU IS ASSOCIATED WITH X-LINKED RENAL-FAILURE WITHOUT X-LINKED RECESSIVE HYPOPHOSPHATEMIC RICKETS
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MUTATIONS OF CLCN5 IN JAPANESE CHILDREN WITH IDIOPATHIC LOW-MOLECULAR-WEIGHT PROTEINURIA, HYPERCALCIURIA AND NEPHROCALCINOSIS
Kidney international
HYPERCALCIURIA AND NEPHROCALCINOSIS IN PATIENTS WITH IDIOPATHIC LOW-MOLECULAR-WEIGHT PROTEINURIA IN JAPAN - IS THE DISEASE IDENTICAL TO DENTS DISEASE IN UNITED-KINGDOM
Nephron
LOW-MOLECULAR-WEIGHT (TUBULAR) PROTEINURIA IS NOT RELATED TO GLYCEMICCONTROL IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS
Diabetes research and clinical practice