Variable renal phenotype in a family with an INF2 mutat ...
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Variable renal phenotype in a f ...
Recent advances in the genetics of glomerular diseases have identified several causative genes of nephrotic syndrome and/or glomerular proteinuria. ...
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Kidney and urinary tract develo ...
Development of the mammalian urogenital system requires a balance between survival and programmed cell death. Pro-survival molecules are crucial in ...
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Effect of diet, enalapril, or l ...
Proteinuria is the main indicator of renal disease progression in many chronic conditions. There is currently little information available on the ef ...
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Clinical outcomes in children w ...
Henoch.Schonlein purpura (HSP) is one of the most common causes of systemic vasculitis in children. The incidence of HSP nephritis (HSPN) among HSP ...
دانلود 1
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Protective effects of Huang Qi ...
Huang Qi Huai (HQH) granules, a mixture of Chinese herbs, contains trametes robiniophila murr, wolfberry fruit, and Polygonatum. We investigated the ...
دانلود 1
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Alport syndrome and leiomyomato ...
Alport syndrome (ATS) is a nephropathy characterized by the association of progressive hematuric nephritis with ultrastructural changes of the glome ...
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Treatment strategies for Henoch ...
The management of Henoch-Schonlein purpura nephritis (HSPN) is controversial. It has been revealed that some patients develop end-stage renal diseas ...
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Four family cases of acute rena ...
Cortinarius poisoning is a rare syndrome that is responsible for a delayed toxic tubulointerstitial nephritis that can induce severe acute or chroni ...
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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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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 ...
دانلود 1
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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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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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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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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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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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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 ...
دانلود 1
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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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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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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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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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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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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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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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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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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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