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Bone evaluation in paediatric chronic kidney disease: clinical practice points from the European Society for Paediatric Nephrology CKD-MBD and Dialysis working groups and CKD-MBD working group of the ERA-EDTA

Nephrology, dialysis, transplantation, 2021-02, Vol.36 (3), p.413-425

2021

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International comparison and time trends of first kidney transplant recipient characteristics across Europe: an ERA Registry study

Nephrology, dialysis, transplantation, 2024-03, Vol.39 (4), p.648-658

2024

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Patient characteristics, treatment history and prognosis of adult survivors of childhood kidney replacement therapy-an ERA Registry study

NEPHROLOGY DIALYSIS TRANSPLANTATION, 2024, Vol.39, p.I166

2024

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Chronic peritoneal dialysis in Turkish children: a multicenter study

Pediatric nephrology (Berlin, West), 2005-05, Vol.20 (5), p.644-651

2005

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Plasma and urine nitric oxide levels in healthy Turkish children

Pediatric nephrology (Berlin, West), 2005-11, Vol.20 (11), p.1605-1609

2005

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High serum adiponectin levels during steroid-responsive nephrotic syndrome relapse

Pediatric nephrology (Berlin, West), 2005-04, Vol.20 (4), p.474-477

2005

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Adiponectin levels and atherosclerotic risk factors in pediatric chronic peritoneal dialysis patients

Peritoneal dialysis international, 2005-07, Vol.25 (4), p.357-361

2005

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Adiponectin levels and arteriosclerotic risk factors in pediatric renal transplant recipients

Pediatric transplantation, 2006-03, Vol.10 (2), p.187-192

2006

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The co-existence of Fabry and celiac diseases: a case report

Pediatric nephrology (Berlin, West), 2004-06, Vol.19 (6), p.679-681

2004

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Digital calciphylaxis progressing to amputation in a child on continuous ambulatory peritoneal dialysis

Annals of tropical paediatrics, 2007-06, Vol.27 (2), p.149-152

2007

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Orthostatic proteinuria as a result of venous compression (nutcracker phenomenon) : a hypothesis testable with modern imaging techniques

Nephrology, dialysis, transplantation, 1999-04, Vol.14 (4), p.826-827

1999

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Cerebral vasculitis in Henoch-Schönlein purpura

Nephrology, dialysis, transplantation, 2000-02, Vol.15 (2), p.246-248

2000

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Evaluation of nutritional status and factors related to malnutrition in children on CAPD

Peritoneal dialysis international, 2003-11, Vol.23 (6), p.557-562

2003

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Measles: A rare communicable disease in a child with renal transplantation

Pediatric transplantation, 2002-10, Vol.6 (5), p.432-434

2002

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Polyarteritis nodosa in a case of familial Mediterranean fever

Pediatric nephrology (Berlin, West), 2004-05, Vol.19 (5), p.536-538

2004

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The effect of CAPD on the lipid profile of pediatric patients

Peritoneal dialysis international, 2000-09, Vol.20 (5), p.568-571

2000

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Severe renal impairment in the case of classic polyarteritis nodosa

Pediatric nephrology (Berlin, West), 2001-02, Vol.16 (2), p.148-150

2001

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Soluble transferrin receptor is not a reliable marker of iron deficiency in pediatric CAPD patients

Peritoneal dialysis international, 2002-09, Vol.22 (5), p.621-625

2002

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Pleurodesis treatment with tetracycline in peritoneal dialysis-complicated hydrothorax

Pediatric nephrology (Berlin, West), 1999-09, Vol.13 (7), p.637

1999

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Impact of dialysis adequacy on cardiac function in pediatric CAPD patients

Peritoneal dialysis international, 2001-07, Vol.21 (4), p.395-400

2001

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Mumps interstitial nephritis : a case report

Pediatric nephrology (Berlin, West), 1999-11, Vol.13 (9), p.930-931

1999

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PSEUDOHYPERKALEMIA DUE TO REACTIVE THROMBOCYTOSIS IN AN INFANT WITH YOLK SAC TUMOR

Pediatric hematology and oncology, 2001, Vol.18 (4), p.303-304

2001

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Mutations in the chloride channel gene, CLCNKB , cause Bartter's syndrome type III

Nature genetics, 1997-10, Vol.17 (2), p.171-178

1997

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Mutations in the Chloride-Bicarbonate Exchanger Gene AE1 Cause Autosomal Dominant but not Autosomal Recessive Distal Renal Tubular Acidosis

Proceedings of the National Academy of Sciences - PNAS, 1998-05, Vol.95 (11), p.6337-6342

1998

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Mutations in ATP6N1B , encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

Nature genetics, 2000-09, Vol.26 (1), p.71-75

2000

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Bone evaluation in paediatric chronic kidney disease: clinical practice points from the European Society for Paediatric Nephrology CKD-MBD and Dialysis working groups and CKD-MBD working group of the ERA-EDTA

International comparison and time trends of first kidney transplant recipient characteristics across Europe: an ERA Registry study

Patient characteristics, treatment history and prognosis of adult survivors of childhood kidney replacement therapy-an ERA Registry study

Chronic peritoneal dialysis in Turkish children: a multicenter study

Plasma and urine nitric oxide levels in healthy Turkish children

High serum adiponectin levels during steroid-responsive nephrotic syndrome relapse

Adiponectin levels and atherosclerotic risk factors in pediatric chronic peritoneal dialysis patients

Adiponectin levels and arteriosclerotic risk factors in pediatric renal transplant recipients

The co-existence of Fabry and celiac diseases: a case report

Digital calciphylaxis progressing to amputation in a child on continuous ambulatory peritoneal dialysis

Orthostatic proteinuria as a result of venous compression (nutcracker phenomenon) : a hypothesis testable with modern imaging techniques

Cerebral vasculitis in Henoch-Schönlein purpura

Evaluation of nutritional status and factors related to malnutrition in children on CAPD

Measles: A rare communicable disease in a child with renal transplantation

Polyarteritis nodosa in a case of familial Mediterranean fever

The effect of CAPD on the lipid profile of pediatric patients

Severe renal impairment in the case of classic polyarteritis nodosa

Soluble transferrin receptor is not a reliable marker of iron deficiency in pediatric CAPD patients

Pleurodesis treatment with tetracycline in peritoneal dialysis-complicated hydrothorax

Impact of dialysis adequacy on cardiac function in pediatric CAPD patients

Mumps interstitial nephritis : a case report

PSEUDOHYPERKALEMIA DUE TO REACTIVE THROMBOCYTOSIS IN AN INFANT WITH YOLK SAC TUMOR

Mutations in the chloride channel gene, CLCNKB , cause Bartter's syndrome type III

Mutations in the Chloride-Bicarbonate Exchanger Gene AE1 Cause Autosomal Dominant but not Autosomal Recessive Distal Renal Tubular Acidosis

Mutations in ATP6N1B , encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

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