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Nephrogenic syndrome of inappropriate antidiuresis

Nephrology, dialysis, transplantation, 2010-09, Vol.25 (9), p.2839-2843

2010

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Switch in FGFR3 and -4 Expression Profile During Human Renal Development May Account for Transient Hypercalcemia in Patients With Sotos Syndrome due to 5q35 Microdeletions

The journal of clinical endocrinology and metabolism, 2014-07, Vol.99 (7), p.E1361-E1367

2014

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Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease

Nephrology, dialysis, transplantation, 2006-10, Vol.21 (10), p.2708-2717

2006

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Lack of specific binding of Shiga-like toxin (verocytotoxin) and non-specific interaction of Shiga-like toxin 2 antibody with human polymorphonuclear leucocytes

Nephrology, dialysis, transplantation, 2007-03, Vol.22 (3), p.749-755

2007

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Proteomic profiling and identification in peritoneal fluid of children treated by peritoneal dialysis

Nephrology, dialysis, transplantation, 2008-07, Vol.23 (7), p.2402-2405

2008

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In vivo degradation of heparan sulfates in the glomerular basement membrane does not result in proteinuria

Journal of the American Society of Nephrology, 2007-03, Vol.18 (3), p.823-832

2007

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Detection of verocytotoxin bound to circulating polymorphonuclear leukocytes of patients with hemolytic uremic syndrome

Journal of the American Society of Nephrology, 2001-04, Vol.12 (4), p.800-806

2001

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IGG and complement receptor expression on peripheral white blood cells in uraemic children

Nephrology, dialysis, transplantation, 2004-09, Vol.19 (9), p.2296-2301

2004

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Verocytotoxin-induced apoptosis of human microvascular endothelial cells

Journal of the American Society of Nephrology, 2001-04, Vol.12 (4), p.767-778

2001

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Hemolytic uremic syndrome attributable to streptococcus pneumoniae infection: A novel cause for secondary protein N-glycan abnormalities

Clinical chemistry (Baltimore, Md.), 2002-05, Vol.48 (5), p.781-784

2002

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Follow‐up and treatment of adults with cystinosis in the Netherlands

Nephrology, dialysis, transplantation, 2002-10, Vol.17 (10), p.1766-1770

2002

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Adult and paediatric patients with minimal change nephrotic syndrome show no major alterations in glomerular expression of sulphated heparan sulphate domains

Nephrology, dialysis, transplantation, 2007-10, Vol.22 (10), p.2886-2893

2007

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Pre-treatment of Dairy and Breast Milk with Sevelamer Hydrochloride and Sevelamer Carbonate to Reduce Phosphate

Peritoneal dialysis international, 2013-09, Vol.33 (5), p.565-572

2013

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No evidence of hearing loss in pseudohypoaldosteronism type 1 patients

Acta oto-laryngologica, 2006, Vol.126 (3), p.237-239

2006

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Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine

Science (American Association for the Advancement of Science), 1994-04, Vol.264 (5155), p.92-95

1994

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Renal transplantation in patients with hemolytic uremic syndrome: high rate of recurrence and increased incidence of acute rejections

Transplantation, 2003-09, Vol.76 (5), p.821

2003

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Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation

Kidney international, 2000-11, Vol.58 (5), p.1870-1875

2000

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Is serum cystatin C the marker of choice to predict glomerular filtration rate in paediatric patients?

Annals of clinical biochemistry, 2003-01, Vol.40 (Pt 1), p.60

2003

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Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ loss

Nephrology, dialysis, transplantation, 2003-03, Vol.18 (3), p.512-516

2003

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Persistent arterial hypotension after bilateral nephrectomy in a 4-month-old infant

Pediatric nephrology (Berlin, West), 2001-07, Vol.16 (7), p.604-605

2001

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Treatment of hyperhomocysteinemia in children on dialysis by folic acid

Pediatric nephrology (Berlin, West), 1999-09, Vol.13 (7), p.583-585

1999

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The clinical spectrum of type IV collagen mutations

Human mutation, 1997, Vol.9 (6), p.477-499

1997

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Interactions of Shiga-like toxin with human peripheral blood monocytes

Pediatric nephrology (Berlin, West), 2007-08, Vol.22 (8), p.1181-1187

2007

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Dominant Isolated Renal Magnesium Loss Is Caused by Misrouting of the Na+,K+-ATPase γ-Subunit

Annals of the New York Academy of Sciences, 2003-04, Vol.986 (1), p.437-443

2003

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Local fibrinolytic therapy with urokinase for peritoneal dialysis catheter obstruction in children

Peritoneal dialysis international, 2002, Vol.22 (1), p.84-86

2002

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Nephrogenic syndrome of inappropriate antidiuresis

Switch in FGFR3 and -4 Expression Profile During Human Renal Development May Account for Transient Hypercalcemia in Patients With Sotos Syndrome due to 5q35 Microdeletions

Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease

Lack of specific binding of Shiga-like toxin (verocytotoxin) and non-specific interaction of Shiga-like toxin 2 antibody with human polymorphonuclear leucocytes

Proteomic profiling and identification in peritoneal fluid of children treated by peritoneal dialysis

In vivo degradation of heparan sulfates in the glomerular basement membrane does not result in proteinuria

Detection of verocytotoxin bound to circulating polymorphonuclear leukocytes of patients with hemolytic uremic syndrome

IGG and complement receptor expression on peripheral white blood cells in uraemic children

Verocytotoxin-induced apoptosis of human microvascular endothelial cells

Hemolytic uremic syndrome attributable to streptococcus pneumoniae infection: A novel cause for secondary protein N-glycan abnormalities

Follow‐up and treatment of adults with cystinosis in the Netherlands

Adult and paediatric patients with minimal change nephrotic syndrome show no major alterations in glomerular expression of sulphated heparan sulphate domains

Pre-treatment of Dairy and Breast Milk with Sevelamer Hydrochloride and Sevelamer Carbonate to Reduce Phosphate

No evidence of hearing loss in pseudohypoaldosteronism type 1 patients

Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine

Renal transplantation in patients with hemolytic uremic syndrome: high rate of recurrence and increased incidence of acute rejections

Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation

Is serum cystatin C the marker of choice to predict glomerular filtration rate in paediatric patients?

Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ loss

Persistent arterial hypotension after bilateral nephrectomy in a 4-month-old infant

Treatment of hyperhomocysteinemia in children on dialysis by folic acid

The clinical spectrum of type IV collagen mutations

Interactions of Shiga-like toxin with human peripheral blood monocytes

Dominant Isolated Renal Magnesium Loss Is Caused by Misrouting of the Na+,K+-ATPase γ-Subunit

Local fibrinolytic therapy with urokinase for peritoneal dialysis catheter obstruction in children

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