Results 181 to 190 of about 1,812 (217)
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Hypouricemia Related to a Hypersecretional Tubulopathy
Nephron, 1983We present 1 patient with hypouricemia and hyperuricosuria. Serum uric acid level ranged between 1.5 and 1.9 mg/dl and uric acid fractional excretion between 20 and 28%. Apart from that the renal function was normal. The pyrazinamide suppression test gave a normal response showing nearly complete suppression of urate excretion.
Dumont, Isabelle, Decaux, Guy
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Light Chain-Mediated Tubulopathies
2011Immunoglobulin light chains are low molecular weight proteins that are filtered through the glomerulus and reabsorbed into the proximal tubular epithelium by binding initially to a heteromeric receptor complex composed of megalin and cubilin. Saturation of this receptor-mediated endocytotic process results in the presence of free light chains in the ...
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Acta medica Austriaca, 1976
1. Defects in transport systems of renal tubules are caused by partial tubular dysfunction without preceeding renal disease. There is a well delineated disturbance for the reabsorption of certain substances. Most commonly the defects in transport of renal tubules are genetically determined. 2.
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1. Defects in transport systems of renal tubules are caused by partial tubular dysfunction without preceeding renal disease. There is a well delineated disturbance for the reabsorption of certain substances. Most commonly the defects in transport of renal tubules are genetically determined. 2.
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Transient renal tubulopathy in a Labrador retriever
Journal of Small Animal Practice, 2001A four‐month‐old male Labrador retriever was presented for polyuria, polydipsia and persistent euglycaemic glucosuria. On referral, diagnostic tests demonstrated abnormal fractional excretions of electrolytes, increased urinary excretion of selected amino acids, mild renal tubular acidosis and mild proteinuria, indicating renal tubular dysfunction ...
P M, Jamieson, M L, Chandler
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Familial progressive renal tubulopathy.
Clinical nephrology, 1992We report herein data on 6 male patients with progressive tubulopathy. These patients belonged to two families: the propositus, his father, a paternal first cousin, two paternal uncles, and a maternal uncle. A 7-year-old proband had mild proteinuria (1 g/day), consisting of beta 2-microglobulin, alpha 1-microglobulin and lysozyme, and aminoaciduria ...
A, Furuse +4 more
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Kaliumverlierende Tubulopathie oder BARTTER-Syndrom?
1966Mit Ausnahme der medikamentos bedingten Hyperkaliurien (Saluretica, Corticosteroide) sind renale Kaliumverluste wesentlich seltener als die enteralen Hypokaliamien. Extrarenal bedingte Hyperkaliurien finden sich hauptsachlich beim Hyperaldosteronismus.
F. Reubi +3 more
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[Non-lithiasic hereditary tubulopathies].
La Revue du praticien, 1997Renal tubular disorders include various clinical conditions wherein the renal tubular reabsorption of an ion or organic solute is significantly decreased. It may concern the renal handling of a single substance, such as glucose or phosphate, a group of substances or a combination of ions and organic substances.
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A clinical approach to tubulopathies in children and young adults
Pediatric Nephrology, 2022Rachael Kermond +2 more
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A Perspective on a Urine-Derived Kidney Tubuloid Biobank from Patients with Hereditary Tubulopathies
Tissue Engineering - Part C: Methods, 2021Marianne C Verhaar
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