Lysosomal enzymuria is a feature of hereditary Fanconi syndrome and is related to elevated CI-mannose-6-P-receptor excretion

Nephrology Dialysis Transplantation

Volumn 23, Issue 9, 2008, Pages 2795-2803

  Norden, Anthony G W ^a   Gardner, Sharon C ^a   Van't Hoff, William ^b   Unwin, Robert J ^c  

^a ADDENBROOKE S HOSPITAL   (United Kingdom)

^b GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^c ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

Author keywords

Cathepsin D; Cation independent mannose 6 phosphate receptor; Dent's disease; Fanconi syndrome; N acetyl D glucosaminidase

Indexed keywords

CATHEPSIN D; LACTATE DEHYDROGENASE; LYSOSOME ENZYME; MANNOSE 6 PHOSPHATE; N ACETYL BETA GLUCOSAMINIDASE; PEPSTATIN; PROCATHEPSIN D; SOMATOMEDIN B RECEPTOR; UNCLASSIFIED DRUG;

ADULT; AFFINITY CHROMATOGRAPHY; APOPTOSIS; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; CREATININE BLOOD LEVEL; CYSTINOSIS; DENT DISEASE; ENZYME LINKED IMMUNOSORBENT ASSAY; ENZYMURIA; FANCONI RENOTUBULAR SYNDROME; GOLGI COMPLEX; HUMAN; KIDNEY PROXIMAL TUBULE; LOWE SYNDROME; LYSOSOME; MEMBRANE TRANSPORT; PRIORITY JOURNAL; URINARY EXCRETION; WESTERN BLOTTING;

ACETYLGLUCOSAMINIDASE; ADULT; BLOTTING, WESTERN; CATHEPSIN D; CHILD; CHROMATOGRAPHY, AFFINITY; CYSTINOSIS; FANCONI SYNDROME; HUMANS; KIDNEY TUBULES, PROXIMAL; L-LACTATE DEHYDROGENASE; LYSOSOMES; PROTEIN TRANSPORT; PROTEINURIA; RECEPTORS, CYTOPLASMIC AND NUCLEAR; YOUNG ADULT;

EID: 53749105716     PISSN: 09310509     EISSN: 14602385     Source Type: Journal    
DOI: 10.1093/ndt/gfm898     Document Type: Article

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