Search Results - "Penza, Rosa"
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Clinical Features and Long-Term Outcome of Nephrotic Syndrome Associated with Heterozygous NPHS1 and NPHS2 Mutations
Published in Clinical journal of the American Society of Nephrology (01-06-2009)“…Mutations in nephrin (NPHS1) and podocin (NPHS2) genes represent a major cause of idiopathic nephrotic syndrome (NS) in children. It is not yet clear whether…”
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2
Unusual pediatric co-morbility: autoimmune thyroiditis and cortico-resistant nephrotic syndrome in a 6-month-old Italian patient
Published in Italian journal of pediatrics (23-10-2012)“…We report on a case of autoimmune thyroiditis in a 6-month-old patient with cortico-resistant nephrotic syndrome. Normal serum levels of thyroid hormons and…”
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3
Low-calcium diet in hypercalciuric enuretic children restores AQP2 excretion and improves clinical symptoms
Published in American journal of physiology. Renal physiology (01-11-2002)“…In this study, we analyzed the effect of a therapeutic intervention in 46 enuretic children, 26 (57%) of whom were hypercalciuric. All the patients (n = 46)…”
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4
End-stage renal disease secondary to IgA nephropathy in recessive dystrophic epidermolysis bullosa: a case report
Published in Pediatric nephrology (Berlin, West) (2008)“…Epidermolysis bullosa (EB) consists of a group of dominant or recessive autosomal diseases characterised by skin and mucosa fragility. The lesions leave…”
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5
Cytokine Pattern and Endothelium Damage Markers in Henoch-Schönlein Purpura
Published in Immunopharmacology and immunotoxicology (01-09-2008)“…In a longitudinal cohort study our aim was to evaluate the cytokine pattern of children affected by Henoch-Schönlein purpura (HSP) and to correlate this…”
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6
Urinary epidermal growth factor, monocyte chemotactic protein-1, and β 2-microglobulin in children with ureteropelvic junction obstruction
Published in Journal of pediatric surgery (01-03-2011)“…Abstract Background/Purpose We demonstrated down-regulation of epidermal growth factor (EGF) and up-regulation of monocyte chemotactic protein-1 (MCP-1) in the…”
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7
Urinary epidermal growth factor, monocyte chemotactic protein-1, and β2-microglobulin in children with ureteropelvic junction obstruction
Published in Journal of pediatric surgery (01-03-2011)“…We demonstrated down-regulation of epidermal growth factor (EGF) and up-regulation of monocyte chemotactic protein-1 (MCP-1) in the renal parenchyma in…”
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8
CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS)
Published in Nephrology, dialysis, transplantation (01-06-2009)“…Background. CD2-associated protein (CD2AP) is a crucial protein for the slit-diaphragm assembly and function. In spite of the fact that CD2AP knockout causes…”
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9
In-vivo administration of CLC-K kidney chloride channels inhibitors increases water diuresis in rats: a new drug target for hypertension?
Published in Journal of hypertension (01-01-2012)“…OBJECTIVEThe human kidney-specific chloride channels ClC-Ka (rodent ClC-K1) and ClC-Kb (rodent ClC-K2) are important determinants of renal function,…”
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10
Urinary aquaporin 2 and calciuria correlate with the severity of enuresis in children
Published in Journal of the American Society of Nephrology (01-10-2000)“…This study examined the hypothesis that nocturnal enuresis might be paralleled by aquaporin 2 (AQP2) urinary excretion. Eighty children who experienced…”
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11
Polydimethylsiloxane (macroplastique® ) injection for vesicoureteral reflux in duplex ureters: A comparison with single renal systems
Published in Journal of pediatric urology (01-10-2011)“…Abstract Objective VUR in patients with a duplex system (DS) is often treated by open surgery. The aim of this study was to evaluate the efficacy of…”
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12
Genetic risk factors in typical haemolytic uraemic syndrome
Published in Nephrology, dialysis, transplantation (01-06-2009)“…Background. Haemolytic uraemic syndrome (HUS) is a disorder characterized by thrombotic microangiopathy, which is caused in ‘typical forms’ by gastrointestinal…”
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13
Endoscopic treatment with polydimethylsiloxane in children with dilating vesico‐ureteric reflux
Published in BJU international (01-04-2006)“…The much‐visited topic of endoscopic treatment of VUR in children with an injectable agent is assessed by authors from Italy. However, in this study using…”
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14
Sodium fraction excretion rate in nocturnal enuresis correlates with nocturnal polyuria and osmolality
Published in The Journal of urology (01-06-2004)“…We verify the sodium fraction excretion rate (FE Na) and potassium fraction excretion (FE K) rates in monosymptomatic nocturnal enuresis. We also correlate FE…”
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15
Normal values of the bioelectrical impedance vector in childhood and puberty
Published in Nutrition (Burbank, Los Angeles County, Calif.) (01-06-2000)“…The purpose of this study was to determine the reference, bivariate, and tolerance intervals of the whole-body impedance vector in Italian children. This was a…”
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16
Risk factors for poor renal prognosis in children with hemolytic uremic syndrome
Published in Pediatric nephrology (Berlin, West) (01-12-2003)“…Many factors have been proposed as predictors of poor renal prognosis in children with hemolytic uremic syndrome (HUS), but their role is still controversial…”
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17
Enuresis subtypes based on nocturnal hypercalciuria: a multicenter study
Published in The Journal of urology (01-10-2003)“…Desmopressin may not be effective for nocturnal enuresis associated with polyuria and hypercalciuria. Nighttime hypercalciuria in an enuretic population from 5…”
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18
Plasma exchange in children with hemolytic-uremic syndrome at risk of poor outcome
Published in American journal of kidney diseases (01-08-1993)“…A retrospective study on the use of plasma exchange in children with hemolytic-uremic syndrome was conducted to compare the renal outcome in treated and…”
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Von Willebrand factor and factor XIII in children with Henoch-Schonlein purpura
Published in Pediatric nephrology (Berlin, West) (01-10-1995)“…levels of von Willebrand factor antigen (vWf:Ag) and factor XIII activity (F XIII) were studied in relation to the severity of clinical symptoms (scored from 0…”
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Conference Proceeding Journal Article -
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Cystinuria type I: Identification of eight new mutations in SLC3A1
Published in Kidney international (01-04-2001)“…Cystinuria type I: Identification of eight new mutations inSLC3A1. Cystinuria is a heritable disorder of amino acid transport characterized by the defective…”
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