Decreased urinary excretion of the ectodomain form of megalin (A-megalin) in children with OCRL gene mutations - Suruda, Chikushi; Tsuji, Shoji; Yamanouchi, Sohsaku; Kimata, Takahisa; Huan, Nguyen Thanh; Kurosawa, Hiroyuki; Hirayama, Yoshiaki; Tsukaguchi, Hiroyasu; Saito, Akihiko; Kaneko, Kazunari (Pediatric nephrology (Berlin, West), 2017)
Keywords: Adolescent; Aging - metabolism; beta 2-Microglobulin - urine; Causes of; Child; Child, Preschool; Children; Complications and side effects; Creatinine; Dent Disease - genetics; Dent Disease - urine; Dent's disease; Development and progression; Enzyme-Linked Immunosorbent Assay; Excretion; Female; Genetic aspects; Health aspects; Humans; Inositol polyphosphate; Low Density Lipoprotein Receptor-Related Protein-2 - analysis; Low Density Lipoprotein Receptor-Related Protein-2 - chemistry; Low Density Lipoprotein Receptor-Related Protein-2 - genetics; Low density lipoprotein receptors; Male; Medicine; Medicine & Public Health; Molecular Weight; Mutation; Nephrology; Oculocerebrorenal Syndrome - genetics; Oculocerebrorenal Syndrome - urine; Original Article; Patients; Pediatric research; Pediatrics; Phosphatase; Phosphoric Monoester Hydrolases - genetics; Physiological aspects; Proteinuria; Proteinuria - genetics; Proteinuria - urine; Urology; Japan; Lowe syndrome; OCRL; Inositol polyphosphate-5-phosphatase; Tubular proteinuria; Dent disease; Megalin