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Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis—a review

European journal of pediatrics, 2009-11, Vol.168 (11), p.1291-1304

2009

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Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)

Human genetics, 2002-12, Vol.111 (6), p.544-547

2002

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Focal segmental glomerulosclerosis in a patient homozygous for a CD2AP mutation

Kidney international, 2007-11, Vol.72 (10), p.1198-1203

2007

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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 for Fibromuscular Dysplasia

American journal of transplantation, 2011-04, Vol.11 (4), p.852-856

2011

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Isolation and Characterization of Verocytotoxin-Producing Escherichia coli O157 Strains from Dutch Cattle and Sheep

Journal of Clinical Microbiology, 1998-04, Vol.36 (4), p.878-882

1998

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Evaluation of the proximal tubular function in hereditary renal Fanconi syndrome

Nephrology, dialysis, transplantation, 2008-09, Vol.23 (9), p.2719-2722

2008

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Hyperhomocysteinemia and other thrombotic risk factors in women with placental vasculopathy

BJOG : an international journal of obstetrics and gynaecology, 2000-06, Vol.107 (6), p.785-791

2000

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Children with chronic renal failure have reduced numbers of memory B cells

Clinical and experimental immunology, 2004-09, Vol.137 (3), p.589-594

2004

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Effects of verocytotoxin-1 on nonadherent human monocytes : Binding characteristics, protein synthesis, and induction of cytokine release

Blood, 1996-07, Vol.88 (1), p.174-183

1996

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Clinical presentation and follow-up of 30 patients with congenital nephrogenic diabetes insipidus

Journal of the American Society of Nephrology, 1999-09, Vol.10 (9), p.1958-1964

1999

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Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

Kidney international, 1998-09, Vol.54 (3), p.720-730

1998

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Trafficking of Shiga toxin/Shiga-like toxin-1 in human glomerular microvascular endothelial cells and human mesangial cells

Kidney international, 2006-12, Vol.70 (12), p.2085-2091

2006

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Tumor Necrosis Factor and Interleukin-1 Induce Expression of the Verocytotoxin Receptor Globotriaosylceramide on Human Endothelial Cells: Implications for the Pathogenesis of the Hemolytic Uremic Syndrome

Blood, 1992-12, Vol.80 (11), p.2755-2764

1992

Volltextzugriff (PDF)

New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels

Journal of the American Society of Nephrology, 1997-02, Vol.8 (2), p.242-248

1997

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Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene

American journal of human genetics, 1994-10, Vol.55 (4), p.648-652

1994

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Effects of TNFα on verocytotoxin cytotoxicity in purified human glomerular microvascular endothelial cells

Kidney international, 1997-04, Vol.51 (4), p.1245-1256

1997

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Recent insights into the structure and functions of heparan sulfate proteoglycans in the human glomerular basement membrane

Nephrology, dialysis, transplantation, 1999-09, Vol.14 (9), p.2119-2129

1999

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Clinical experience with icodextrin in children: ultrafiltration profiles and metabolism

Pediatric nephrology (Berlin, West), 2000-11, Vol.15 (1-2), p.21-24

2000

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Thin glomerular basement membrane disease

Kidney international, 2001-08, Vol.60 (2), p.799-800

Monnens, Leo A.H.

2001

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Defective proximal tubular function in a patient with I-cell disease

Pediatric nephrology (Berlin, West), 2003-08, Vol.18 (8), p.830-832

2003

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Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin

Kidney international, 1999-04, Vol.55 (4), p.1217-1224

1999

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Characterization of verocytotoxin-producing Escherichia coli O157 isolates from patients with haemolytic uraemic syndrome in Western Europe

Epidemiology and infection, 1995-08, Vol.115 (1), p.1-3

1995

Volltextzugriff (PDF)

Advances in haemolytic uraemic syndrome

Archives of disease in childhood, 1998-02, Vol.78 (2), p.190-193

1998

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Renal transplant nephrectomy in children: Can an aggressive approach be recommended?

Pediatric transplantation, 2004-12, Vol.8 (6), p.561-564

2004

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Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis—a review

Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)

Focal segmental glomerulosclerosis in a patient homozygous for a CD2AP mutation

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

Renal Transplantation for Fibromuscular Dysplasia

Isolation and Characterization of Verocytotoxin-Producing Escherichia coli O157 Strains from Dutch Cattle and Sheep

Evaluation of the proximal tubular function in hereditary renal Fanconi syndrome

Hyperhomocysteinemia and other thrombotic risk factors in women with placental vasculopathy

Children with chronic renal failure have reduced numbers of memory B cells

Effects of verocytotoxin-1 on nonadherent human monocytes : Binding characteristics, protein synthesis, and induction of cytokine release

Clinical presentation and follow-up of 30 patients with congenital nephrogenic diabetes insipidus

Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

Trafficking of Shiga toxin/Shiga-like toxin-1 in human glomerular microvascular endothelial cells and human mesangial cells

Tumor Necrosis Factor and Interleukin-1 Induce Expression of the Verocytotoxin Receptor Globotriaosylceramide on Human Endothelial Cells: Implications for the Pathogenesis of the Hemolytic Uremic Syndrome

New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels

Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene

Effects of TNFα on verocytotoxin cytotoxicity in purified human glomerular microvascular endothelial cells

Recent insights into the structure and functions of heparan sulfate proteoglycans in the human glomerular basement membrane

Clinical experience with icodextrin in children: ultrafiltration profiles and metabolism

Thin glomerular basement membrane disease

Defective proximal tubular function in a patient with I-cell disease

Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin

Characterization of verocytotoxin-producing Escherichia coli O157 isolates from patients with haemolytic uraemic syndrome in Western Europe

Advances in haemolytic uraemic syndrome

Renal transplant nephrectomy in children: Can an aggressive approach be recommended?

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