Search Results - "MARANGELLA, M"
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Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment
Published in Nephrology, dialysis, transplantation (01-05-2012)“…Primary hyperoxaluria Type 1 is a rare autosomal recessive inborn error of glyoxylate metabolism, caused by a deficiency of the liver-specific enzyme…”
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Storia naturale della iperossaluria primitiva
Published in Giornale di clinica nefrologica e dialisi (24-01-2018)“…Abstract non disponibile…”
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Effects of potassium citrate supplementation on bone metabolism
Published in Calcified tissue international (01-04-2004)“…Western diets rich in animal protein result in long-term acid loading that, despite corresponding increases in net renal acid excretion, may induce a chronic…”
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Italian Society of Rheumatology recommendations for the management of gout
Published in Reumatismo (28-03-2013)“…Gout is the most common arthritis in adults. Despite the availability of valid therapeutic options, the management of patients with gout is still suboptimal…”
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AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria
Published in Journal of the American Society of Nephrology (01-10-2001)“…Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disorder that is caused by a deficiency of alanine: glyoxylate aminotransferase (AGT), which is…”
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Primary hyperoxaluria: report of an Italian family with clear sex conditioned penetrance
Published in Urolithiasis (01-12-2008)“…We report the clinical and genetic study of a primary hyperoxaluria type I (PH1) family with two sisters homozygous for p.Gly170Arg who are still asymptomatic…”
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Autonomic neuropathy and QT interval in hemodialysed patients
Published in Clinical autonomic research (01-08-2004)“…QT interval prolongation increases the risk of ventricular arrhythmias and sudden death in diabetic autonomic neuropathy and ischemic heart disease. In…”
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Iperparatiroidismo primitivo e nefrolitiasi: vi è spazio per i calciomimetici?
Published in Giornale di clinica nefrologica e dialisi (24-01-2018)“…Abstract non disponibile…”
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Diagnostic biologique de l’hyperparathyroïdisme
Published in Immuno-analyse & biologie spécialisée (01-10-2008)“…Parathyroid hormone (PTH) has important applications in the clinical practice both primary (PHP) and secondary (SHP) hyperprathyroidisms. However, assays of…”
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Urine and stone analysis for the investigation of the renal stone former: a consensus conference
Published in Urolithiasis (01-02-2021)“…The Consensus Group deliberated on a number of questions concerning urine and stone analysis over a period of months, and then met to develop consensus. The…”
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Uric acid elimination in the urine. Pathophysiological implications
Published in Contributions to nephrology (2005)“…Uric acid, a weak organic acid, has very low pH-dependent solubility in aqueous solutions. About 70% of urate elimination occurs in urine, the kidney standing…”
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Thresholds of serum calcium oxalate supersaturation in relation to renal function in patients with or without primary hyperoxaluria
Published in Nephrology, dialysis, transplantation (1993)“…Systemic oxalosis is a constant feature in patients with primary hyperoxaluria type 1 (PH1) and chronic renal failure (CRF) and is not prevented by regular…”
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CAPD with an amino acid dialysis solution: A long-term, cross-over study
Published in Kidney international (01-05-1989)“…CAPD with an amino acid dialysis solution: A long-term, cross-over study. This prospective cross-over study was undertaken to evaluate the safety and efficacy…”
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International Alliance of Urolithiasis (IAU) guidelines on the metabolic evaluation and medical management of urolithiasis
Published in Urolithiasis (01-12-2022)“…The aim of this study was to construct the fourth in a series of guidelines on the treatment of urolithiasis by the International Alliance of Urolithiasis…”
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VDRA therapy is associated with improved survival in dialysis patients with serum intact PTH ≤150 pg/mL: results of the Italian FARO Survey
Published in Nephrology, dialysis, transplantation (01-09-2012)“…Chronic kidney disease (CKD) patients affected by mineral bone disorders (MBD) have higher rates of all-cause and cardiovascular-related mortality…”
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The clinical significance of assessment of serum calcium oxalate saturation in the hyperoxaluria syndromes
Published in Nephrology, dialysis, transplantation (1995)“…Estimating calcium oxalate saturation (beta CaOx) in body fluids is proposed as a simple and reproducible procedure to assess the risk of systemic oxalosis in…”
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Gene symbol: AGXT. Disease: primary hyperoxaluria type I
Published in Human genetics (01-05-1999)Get full text
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PTH measurement: where do we stand?
Published in Giornale italiano di nefrologia (01-09-2009)“…PTH measurements are widely used by nephrologists because parathyroid function is frequently altered in uremic patients, with clinical implications for bone…”
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Iperparatiroidismo primitivo e nefrolitiasi: vi è spazio per i calciomimetici?
Published in Giornale di clinica nefrologica e dialisi (01-01-2018)“…Abstract non disponibile…”
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Journal Article