# عنوان نوع فایل سایز فایل بازدید دانلود امتیاز قیمت (تومان)
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Microvascular disease in children and adolescents with type 1 diabetes and obesity
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Abdominal pain in a female adolescent: answer
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Fetal environment, epigenetics, and pediatric renal disease
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A 10-year-old boy with dark urine and acute kidney injury: answer
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Defining and redefining the nephron progenitor population
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Imaging of the urinary tract: the role of CT and MRI
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Pathogenesis, diagnosis and management of hyperkalemia
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Renal manifestations of patients with MYH9-related disorders
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Hypochloremic metabolic alkalosis and failure to thrive: answer
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An unusual case of hyperkalaemia in infancy: answer
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The impact of pediatric nephrotic syndrome on families
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Semaphorins in kidney development and disease: modulators of ureteric bud branching, vascular morphogenesis, and podocyte-endothelial crosstalk
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Age-related stature and linear body segments in children with X-linked hypophosphatemic rickets
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Clinical and laboratory features of Macedonian children with OCRL mutations
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Unilateral localized cystic kidney: Answer
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Letter to the Editor regarding the article ‘‘Anorectal malformations and neurospinal dysraphism: is this association a major risk for continence?’’
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HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort
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Plasma from a case of recurrent idiopathic FSGS perturbs non-muscle myosin IIA (MYH9 protein) in human podocytes
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Nephrotic syndrome in The Netherlands: a population-based cohort study and a review of the literature
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Glomerular basement membrane composition and the filtration barrier
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An unusual case of gross hematuria with acute renal failure: answer
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Acute reversible changes of brachial-ankle pulse wave velocity in children with acute poststreptococcal glomerulonephritis
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Four family cases of acute renal failure: answer
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Treatment strategies for Henoch-Schِnlein purpura nephritis by histological and clinical severity
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Alport syndrome and leiomyomatosis: the first deletion extending beyond COL4A6 intron 2
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Microvascular disease in children and adolescents  with type 1 diabetes and obesity

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 ...

199.02 KB
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Abdominal pain in a female adolescent: answer

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 ...

139.90 KB
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Fetal environment, epigenetics, and pediatric renal disease

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 ...

258.64 KB
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A 10-year-old boy with dark urine and acute kidney  injury: answer

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 ...

93.04 KB
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Defining and redefining the nephron progenitor population

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 ...

574.44 KB
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Imaging of the urinary tract: the role of CT and MRI

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 ...

411.61 KB
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Pathogenesis, diagnosis and management of hyperkalemia

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 ...

173.29 KB
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Renal manifestations of patients  with MYH9-related disorders

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 ...

244.43 KB
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Hypochloremic metabolic alkalosis and failure to thrive:  answer

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 ...

59.66 KB
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An unusual case of hyperkalaemia in infancy: answer

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 ...

70.46 KB
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The impact of pediatric nephrotic syndrome on families

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 ...

135.65 KB
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Semaphorins in kidney development and disease: modulators  of ureteric bud branching, vascular morphogenesis,  and podocyte-endothelial crosstalk

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 ...

364.88 KB
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Age-related stature and linear body segments in children  with X-linked hypophosphatemic rickets

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 ...

384.72 KB
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Clinical and laboratory features of Macedonian  children with OCRL mutations

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 ...

148.07 KB
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Unilateral localized cystic kidney: Answer

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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Letter to the Editor regarding the article ‘‘Anorectal  malformations and neurospinal dysraphism: is this association  a major risk for continence?’’

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 ...

110.40 KB
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HNF1B and PAX2 mutations are a common cause of renal  hypodysplasia in the CKiD cohort

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 ...

238.79 KB
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Plasma from a case of recurrent idiopathic FSGS perturbs  non-muscle myosin IIA (MYH9 protein) in human podocytes

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 ...

1.19 MB
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Nephrotic syndrome in The Netherlands: a population-based  cohort study and a review of the literature

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 ...

150.51 KB
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Glomerular basement membrane composition  and the filtration barrier

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 ...

114.78 KB
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An unusual case of gross hematuria with acute renal  failure: answer

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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Acute reversible changes of brachial-ankle pulse wave  velocity in children with acute poststreptococcal  glomerulonephritis

Acute reversible changes of bra ...

Acute poststreptococcal glomerulonephritis (APSGN) is the most common form of postinfectious nephritis worldwide. The relationship between inflammat ...

136.17 KB
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Four family cases of acute renal failure: answer

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 ...

135.45 KB
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Treatment strategies for Henoch-Schِnlein purpura  nephritis by histological and clinical severity

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 ...

269.50 KB
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Alport syndrome and leiomyomatosis: the first deletion  extending beyond COL4A6 intron 2

Alport syndrome and leiomyomato ...

Alport syndrome (ATS) is a nephropathy characterized by the association of progressive hematuric nephritis with ultrastructural changes of the glome ...

466.33 KB
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