TRPC channel modulation in podocytes—inching toward no ...
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TRPC channel modulation in podo ...
Glomerular kidney disease is a major healthcare burden and considered to represent a sum of disorders that evade a refined and effective treatment. ...
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Patterning and early cell linea ...
Specification of the intermediate mesoderm and the epithelial derivatives that will make the mammalian kidney depends on the concerted action of man ...
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aHUS caused by complement dysre ...
Atypical hemolytic uremic syndrome (aHUS) is a heterogeneous disease that is caused by defective complement regulation in over 50% of cases. Mutatio ...
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Microvascular disease in childr ...
The incidence of type 1 diabetes (T1D) is increasing worldwide and is associated with a significant burden, mainly related to the development of vas ...
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Abdominal pain in a female adol ...
Differential diagnosis of abdominal pain in a female teenager with autosomal dominant polycystic kidney disease (ADPKD) and insulin-dependent diabet ...
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Fetal environment, epigenetics, ...
The notion that some adult diseases may have their origins in utero has recently captured scientists’ attention. Some of these effects persist acros ...
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A 10-year-old boy with dark uri ...
Mitochondrial fatty acid â-oxidation (FAO) is essential for energy homeostasis in skeletal muscle under conditions that require simultaneous glucose ...
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Defining and redefining the nep ...
It has long been appreciated that the mammalian kidney arises via reciprocal interactions between an epithelial ureteric epithelium and the surround ...
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Imaging of the urinary tract: t ...
Computed tomography (CT) and magnetic resonance imaging (MRI) are increasingly valuable tools for assessing the urinary tract in adults and children ...
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Pathogenesis, diagnosis and man ...
Hyperkalemia is a potentially life-threatening condition in which serum potassium exceeds 5.5 mmol/l. It can be caused by reduced renal excretion, e ...
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Renal manifestations of patient ...
MYH9-related disorders are a group of autosomal, dominantly inherited disorders caused by mutations of the MYH9 gene, which encodes the non-muscle m ...
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Hypochloremic metabolic alkalos ...
CLD is a rare autosomal recessive disease occurring mainly in people in Arabian countries, Finland, and Poland [1–3]. It is characterized by unremit ...
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An unusual case of hyperkalaemi ...
PHA type II is a rare but interesting disorder because of the unusual association of hypertension with hyperkalemia which appears to indicate a disa ...
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The impact of pediatric nephrot ...
The objective of our study was to assess the psychologic and economic effects of pediatric nephrotic syndrome (NS) on caregivers. Caregivers of 50 c ...
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Semaphorins in kidney developme ...
Semaphorins are guidance proteins that play important roles in organogenesis and disease. Expression of class 3 semaphorins and their receptors is r ...
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Age-related stature and linear ...
Children with X-linked hypophosphatemic rickets (XLH) are prone to severe stunting. A multicenter mixed-longitudinal study was conducted to assess a ...
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Clinical and laboratory feature ...
OCRL mutations, which are a hallmark of Lowe syndrome, have recently been found in patients with isolated renal phenotype (Dent-2 disease). In this ...
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Unilateral localized cystic kid ...
ADPKD is the clinical manifestation of a genetic defect that is typically thought to be a bilateral renal cystic disease of adults, since children a ...
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Letter to the Editor regarding ...
This letter is in reference to the article by Di Cesare et al. [1], regarding the association of anorectal malformations (ARMs) and neurospinal dysr ...
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HNF1B and PAX2 mutations are a ...
Malformations of the kidney and lower urinary tract are the most frequent cause of end-stage renal disease in children. Mutations in HNF1آ and PAX2 ...
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Plasma from a case of recurrent ...
The MYH9 gene encodes a non-muscle myosin IIA heavy chain (NMMHC-IIA) expressed in podocytes. Heterozygous MYH9 mutations cause a set of overlapping ...
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Nephrotic syndrome in The Nethe ...
Nephrotic syndrome (NS) is a clinical diagnosis with proteinuria, hypoalbuminaemia and oedema. NS is rare in children, and its incidence in The Neth ...
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Glomerular basement membrane co ...
The glomerular basement membrane (GBM) is an especially thick basement membrane that contributes importantly to the kidney’s filtration barrier. The ...
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An unusual case of gross hematu ...
Acute renal failure (ARF) is a rare but well-known complication of massive gross hematuria and has been reported in immunoglobulin (Ig)A nephropathy ...
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Acute reversible changes of bra ...
Acute poststreptococcal glomerulonephritis (APSGN) is the most common form of postinfectious nephritis worldwide. The relationship between inflammat ...
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