# عنوان نوع فایل سایز فایل بازدید دانلود امتیاز قیمت (تومان)
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Should we consider MMF therapy after rituximab for nephrotic syndrome?
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Parathyroid hormone levels in long-term renal transplant children and adolescents
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Comparative clinical outcomes between pediatric and young adult dialysis patients
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Novel developments in thrombotic microangiopathies: is there a common link between hemolytic uremic syndrome and thrombotic thrombocytic purpura?
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Physiopathology of idiopathic nephrotic syndrome: lessons from glucocorticoids and epigenetic perspectives
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The role of serum myeloid-related protein 8/14 complex in Henoch–Schِnlein purpura nephritis
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Phenotypic variability of Bardet-Biedl syndrome: focusing on the kidney
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Microalbuminuria: causes and implications
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Women and Alport syndrome
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Dyslipidemia in children with CKD: should we treat with statins?
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Cardiorespiratory fitness in young adults with a history of renal transplantation in childhood
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Maintenance therapy with mycophenolate mofetil after rituximab in pediatric patients with steroid-dependent nephrotic syndrome
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Nephrotic syndrome in infancy can spontaneously resolve
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Insufficient protection by Neisseria meningitidis vaccination alone during eculizumab therapy
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The role of molecular genetics in diagnosing familial hematuria(s)
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Epidemiology of chronic kidney disease in children
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Weight or body surface area dosing of steroids in nephrotic syndrome: is there an outcome difference?
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Rhabdomyolysis: pathogenesis of renal injury and management
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A patient with polyuria and hydronephrosis: answer
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Heart ventricular activation in VAT difference maps from children with chronic kidney disease
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The impact of vesicoureteral reflux treatment on the incidence of urinary tract infection
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Postnatal trends in creatinemia and its covariates in extremely low birth weight (ELBW) neonates
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Neurological development in 21 children on peritoneal dialysis in infancy
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Posterior reversible encephalopathy syndrome in children with kidney diseases
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Why is hypercalciuria absent at diagnosis in some children with ATP6V1B1 mutation?
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Should we consider MMF therapy after rituximab  for nephrotic syndrome?

Should we consider MMF therapy ...

The management of steroid-dependent nephrotic syndrome, especially in patients who have failed to respond to cytotoxic drugs, such as cyclophosphami ...

106.10 KB
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Parathyroid hormone levels in long-term renal transplant  children and adolescents

Parathyroid hormone levels in l ...

Secondary hyperparathyroidism is a common complication of chronic renal failure. Kidney transplantation corrects renal insufficiency and most metabo ...

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Comparative clinical outcomes between pediatric and young  adult dialysis patients

Comparative clinical outcomes b ...

Published data on the comparative achievement of The Kidney Disease Dialysis Outcome Quality Initative (KDOQI) recommended clinical performance targ ...

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Novel developments in thrombotic microangiopathies:  is there a common link between hemolytic uremic syndrome  and thrombotic thrombocytic purpura?

Novel developments in thromboti ...

Thrombotic microangiopathies (TMA) represent a spectrum of related disorders associated with newly formed thrombi that block perfusion and thus affe ...

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Physiopathology of idiopathic nephrotic syndrome:  lessons from glucocorticoids and epigenetic perspectives

Physiopathology of idiopathic n ...

Idiopathic nephrotic syndrome (INS) has been studied for decades in attempt to understand the physiopathological mechanisms explaining the disease. ...

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The role of serum myeloid-related protein 8/14 complex  in Henoch–Schِnlein purpura nephritis

The role of serum myeloid-relat ...

Myeloid-related protein (MRP) 8/14 complex is a marker of monocyte and neutrophil activation. We evaluated whether serum MRP8/14 complex is associat ...

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Phenotypic variability of Bardet-Biedl syndrome: focusing  on the kidney

Phenotypic variability of Barde ...

Bardet-Biedl syndrome (BBS) is a multisystemic developmental disorder diagnosed on the basis of the presence of obesity, retinal defects, polydactyl ...

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Microalbuminuria: causes and implications

Microalbuminuria: causes and im ...

Management strategies are increasingly focused on tackling the increasing burden of cardiovascular disease worldwide. Microalbuminuria is a powerful ...

263.85 KB
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Women and Alport syndrome

Women and Alport syndrome

X-linked Alport syndrome (XLAS) is caused by mutations in type IV collagen causing sensorineural hearing loss, eye abnormalities, and progressive ki ...

181.31 KB
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Dyslipidemia in children with CKD:  should we treat with statins?

Dyslipidemia in children with C ...

Dyslipidemia has been shown to be a risk factor for increased cardiovascular morbidity and mortality in adult patients with chronic kidney disease ( ...

142.01 KB
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Cardiorespiratory fitness in young adults with a history  of renal transplantation in childhood

Cardiorespiratory fitness in yo ...

Limited knowledge exists on cardiorespiratory fitness (CR fitness) in adults having a renal transplant (Rtx) during childhood. Our aim was to assess ...

287.76 KB
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Maintenance therapy with mycophenolate mofetil  after rituximab in pediatric patients with steroid-dependent  nephrotic syndrome

Maintenance therapy with mycoph ...

Rituximab (RTX) has a significant steroidsparing effect in children with steroid-dependent nephrotic syndrome (SDNS). However, patients are likely t ...

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Nephrotic syndrome in infancy can spontaneously resolve

Nephrotic syndrome in infancy c ...

Nephrotic syndrome in the first year of life (NSFL) is a heterogeneous group of disorders, the management of which is supportive, as most patients d ...

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Insufficient protection by Neisseria meningitidis vaccination  alone during eculizumab therapy

Insufficient protection by Neis ...

Sirs, Spurred by the reported spectacular results of eculizumab treatment in atypical hemolytic uremic syndrome (aHUS) due to aberrations in the co ...

دانلود 1
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The role of molecular genetics in diagnosing  familial hematuria(s)

The role of molecular genetics ...

Familial microscopic hematuria (MH) of glomerular origin represents a heterogeneous group of monogenic conditions involving several genes, some of w ...

323.85 KB
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Epidemiology of chronic kidney disease in children

Epidemiology of chronic kidney ...

In the past 30 years there have been major improvements in the care of children with chronic kidney disease (CKD). However, most of the available ep ...

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Weight or body surface area dosing of steroids in nephrotic  syndrome: is there an outcome difference?

Weight or body surface area dos ...

Although prednisone is the treatment of choice for nephrotic syndrome (NS) in childhood, the dosing regimen varies between 60 mg/m2/day, as recommen ...

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Rhabdomyolysis: pathogenesis of renal injury  and management

Rhabdomyolysis: pathogenesis of ...

Rhabdomyolysis refers to the breakdown of skeletal muscle due to either a physical, biological, or toxic injury that leads to leakage of muscle cont ...

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A patient with polyuria and hydronephrosis: answer

A patient with polyuria and hyd ...

The case demonstrates the importance of assessing NDI and hydronephrosis separately. Hydronephrosis is a recognised complication of primary NDI and ...

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Heart ventricular activation in VAT difference maps  from children with chronic kidney disease

Heart ventricular activation in ...

Children with chronic kidney disease (CKD) are affected by cardiovascular complications, including disturbances in the intraventricular conduction s ...

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The impact of vesicoureteral reflux treatment  on the incidence of urinary tract infection

The impact of vesicoureteral re ...

Vesicoureteral reflux (VUR) is a heterogeneous disease and its management remains one of the most controversial topics in pediatrics. Management opt ...

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Postnatal trends in creatinemia and its covariates  in extremely low birth weight (ELBW) neonates

Postnatal trends in creatinemia ...

To document trends and covariates of creatinemia (Scr) in extremely low birth weight (ELBW, < 1,000 g) neonates, maternal characteristics [betametha ...

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Neurological development in 21 children on peritoneal  dialysis in infancy

Neurological development in 21 ...

Few studies have focused on the neurodevelopment of infants on peritoneal dialysis (PD). Infants are the most demanding patient group on PD and thus ...

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Posterior reversible encephalopathy syndrome in children  with kidney diseases

Posterior reversible encephalop ...

Posterior reversible encephalopathy syndrome (PRES) was originally used to describe a reversible, predominantly posterior leukoencephalopathy in pat ...

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Why is hypercalciuria absent at diagnosis in some children  with ATP6V1B1 mutation?

Why is hypercalciuria absent at ...

We try to explain why hypercalciuria is absent at diagnosis in some children with an ATP6V1B1 mutation. A 5-month-old girl presented with distal ren ...

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