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Factors influencing blood pressure and microalbuminuria in children with type 1 diabetes mellitus: salt or sugar?

Pediatric nephrology (Berlin, West), 2020-07, Vol.35 (7), p.1267-1276

2020

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PROGRESS STUDY: Progression of chronic kidney disease in children and heat shock proteins

Cell stress & chaperones, 2021-11, Vol.26 (6), p.973-987

2021

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Treatment of ichthyosis and hypernatremia in a patient with Netherton syndrome with a SPINK5 c.153delT mutation using kallikrein inhibiting ointment

International journal of dermatology, 2017-01, Vol.56 (1), p.106-108

2017

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Magnetic resonance imaging based kidney volume assessment for risk stratification in pediatric autosomal dominant polycystic kidney disease

Frontiers in pediatrics, 2024, Vol.12, p.1357365-1357365

2024

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Cardiometabolic Risk Factors in Pediatric Kidney Transplant Recipients

Turkish archives of pediatrics, 2023-03, Vol.58 (2), p.220-225

2023

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HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract

Pediatric nephrology (Berlin, West), 2023-03, Vol.38 (3), p.933-934

2023

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Effects of clinoptilolite treatment on oxidative stress after partial hepatectomy in rats

Asian journal of surgery, 2011-10, Vol.34 (4), p.153-157

2011

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A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature

Pediatric nephrology (Berlin, West), 2023-03, Vol.38 (3), p.711-719

2023

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A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase

Pediatric nephrology (Berlin, West), 2023-03, Vol.38 (3), p.711

2023

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Effects of Ganoderma lucidum on Obstructive Jaundice-induced Oxidative Stress

Asian journal of surgery, 2010-10, Vol.33 (4), p.173-180

2010

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A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract

Clinical genetics, 2020-10, Vol.98 (4), p.390-395

2020

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Clinical and subclinical acute kidney injury in children with mild-to-moderate COVID-19

Pediatric research, 2023-02, Vol.93 (3), p.654-660

2023

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A broad clinical spectrum of PLC[epsilon]1-related kidney disease and intrafamilial variability

Pediatric nephrology (Berlin, West), 2022-08, Vol.37 (8), p.1855

2022

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Strong mesangial IgA staining—does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Answers

Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.2043-2045

2021

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Natural history of patients with infantile nephrolithiasis: what are the predictors of surgical intervention?

Pediatric nephrology (Berlin, West), 2021-04, Vol.36 (4), p.939-944

2021

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Strong mesangial IgA staining—does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Questions

Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.2039-2041

2021

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Increased Carotid Intima-media Thickness and Its Association with Carbohydrate Metabolism and Adipocytokines in Children Treated with Recombinant Growth Hormone

Journal of clinical research in pediatric endocrinology, 2023-03, Vol.15 (1), p.69-80

2023

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Increased risk for kidney sequelae surrogates in survivors of Wilms tumor

Pediatric nephrology (Berlin, West), 2022-10, Vol.37 (10), p.2415-2426

2022

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Humoral and cellular immune response to SARS-CoV-2 mRNA BNT162b2 vaccine in pediatric kidney transplant recipients compared with dialysis patients and healthy children

Pediatric nephrology (Berlin, West), 2023-07, Vol.38 (7), p.2199-2208

2023

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MO026CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

Nephrology, dialysis, transplantation, 2021-05, Vol.36 (Supplement_1)

2021

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Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers

Pediatric nephrology (Berlin, West), 2019, Vol.34 (1), p.77-79

2019

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Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions

Pediatric nephrology (Berlin, West), 2019, Vol.34 (1), p.75-76

2019

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Predictors of poor kidney outcome in children with C3 glomerulopathy

Pediatric nephrology (Berlin, West), 2021-05, Vol.36 (5), p.1195-1205

2021

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Evaluation of non-infectious complications of peritoneal dialysis in children: a multicenter study

Pediatric nephrology (Berlin, West), 2021-02, Vol.36 (2), p.417-423

2021

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Spatial Distribution of Macrophage Subtypes Among Rejection Subtypes in Renal Transplant Biopsies by Dual Immunohistochemistry

Applied immunohistochemistry & molecular morphology, 2023-04, Vol.31 (4), p.224

2023

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Factors influencing blood pressure and microalbuminuria in children with type 1 diabetes mellitus: salt or sugar?

PROGRESS STUDY: Progression of chronic kidney disease in children and heat shock proteins

Treatment of ichthyosis and hypernatremia in a patient with Netherton syndrome with a SPINK5 c.153delT mutation using kallikrein inhibiting ointment

Magnetic resonance imaging based kidney volume assessment for risk stratification in pediatric autosomal dominant polycystic kidney disease

Cardiometabolic Risk Factors in Pediatric Kidney Transplant Recipients

HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract

Effects of clinoptilolite treatment on oxidative stress after partial hepatectomy in rats

A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature

A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase

Effects of Ganoderma lucidum on Obstructive Jaundice-induced Oxidative Stress

A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract

Clinical and subclinical acute kidney injury in children with mild-to-moderate COVID-19

A broad clinical spectrum of PLC[epsilon]1-related kidney disease and intrafamilial variability

Strong mesangial IgA staining—does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Answers

Natural history of patients with infantile nephrolithiasis: what are the predictors of surgical intervention?

Strong mesangial IgA staining—does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Questions

Increased Carotid Intima-media Thickness and Its Association with Carbohydrate Metabolism and Adipocytokines in Children Treated with Recombinant Growth Hormone

Increased risk for kidney sequelae surrogates in survivors of Wilms tumor

Humoral and cellular immune response to SARS-CoV-2 mRNA BNT162b2 vaccine in pediatric kidney transplant recipients compared with dialysis patients and healthy children

MO026CLINICAL AND MUTATIONAL SPECTRUM OF CHILDREN WITH AUTOSOMAL RECESSIVE AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers

Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions

Predictors of poor kidney outcome in children with C3 glomerulopathy

Evaluation of non-infectious complications of peritoneal dialysis in children: a multicenter study

Spatial Distribution of Macrophage Subtypes Among Rejection Subtypes in Renal Transplant Biopsies by Dual Immunohistochemistry

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