Published in Ned Tijdschr Geneeskd on May 13, 1989
Requirement of human renal water channel aquaporin-2 for vasopressin-dependent concentration of urine. Science (1994) 4.27
Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome. Nat Genet (1994) 2.12
Focal segmental glomerulosclerosis in a patient homozygous for a CD2AP mutation. Kidney Int (2007) 1.93
Herpes simplex virus type 1 glycoprotein E is not indispensable for viral infectivity. J Virol (1987) 1.92
Effects of oral and intramuscular vitamin K prophylaxis on vitamin K1, PIVKA-II, and clotting factors in breast fed infants. Arch Dis Child (1992) 1.86
An unusual defective genotype derived from herpes simplex virus strain ANG. Intervirology (1977) 1.75
Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome. Hum Mol Genet (1994) 1.69
Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain. Kidney Int (1998) 1.66
Origin of two different classes of defective HSV-1 Angelotti DNA. Nucleic Acids Res (1979) 1.62
Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin. Kidney Int (1999) 1.61
The glycosaminoglycan content of renal basement membranes in the congenital nephrotic syndrome of the Finnish type. Pediatr Nephrol (1992) 1.55
Characterization of verocytotoxin-producing Escherichia coli O157 isolates from patients with haemolytic uraemic syndrome in Western Europe. Epidemiol Infect (1995) 1.54
[Prevalence of hemorrhages due to vitamin K deficiency in The Netherlands, 1992-1994]. Ned Tijdschr Geneeskd (1996) 1.54
Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus. Nat Genet (1992) 1.51
Effects of verocytotoxin-1 on nonadherent human monocytes: binding characteristics, protein synthesis, and induction of cytokine release. Blood (1996) 1.51
Prevention of vitamin K deficiency in infancy by weekly administration of vitamin K. Acta Paediatr (1993) 1.47
Occurrence of verocytotoxin-producing Escherichia coli O157 on Dutch dairy farms. J Clin Microbiol (1998) 1.47
Expression of hepatitis B virus X protein in HBV-infected human livers and hepatocellular carcinomas. Hepatology (1998) 1.46
Passive immune protection by herpes simplex virus-specific monoclonal antibodies and monoclonal antibody-resistant mutants altered in pathogenicity. J Virol (1985) 1.45
Isolation and characterization of verocytotoxin-producing Escherichia coli O157 strains from Dutch cattle and sheep. J Clin Microbiol (1998) 1.45
Intraperitoneal administration of recombinant human erythropoietin in children on continuous ambulatory peritoneal dialysis. Eur J Pediatr (1992) 1.44
Fibrinolytic responses to 1-desamino-8-D-arginine-vasopressin in patients with congenital nephrogenic diabetes insipidus. Nephron (1990) 1.42
Renal allograft rejection and antibodies to epithelial cells. Lancet (1992) 1.42
Immunogenicity of herpes simplex virus glycoproteins gC and gB and their role in protective immunity. J Virol (1984) 1.39
Adequate dialysis? Measurement of KT/V in a pediatric peritoneal dialysis population. Perit Dial Int (1997) 1.39
Rectal atresia: pathogenesis and operative treatment. Pediatr Surg Int (2013) 1.39
The midline cervical cleft. J Pediatr Surg (1991) 1.37
[Evaluation of various forms of vitamin-K prophylaxis in breastfed infants]. Ned Tijdschr Geneeskd (1993) 1.37
Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit. Nat Genet (2000) 1.35
Effects of TNF alpha on verocytotoxin cytotoxicity in purified human glomerular microvascular endothelial cells. Kidney Int (1997) 1.35
Clinical presentation and follow-up of 30 patients with congenital nephrogenic diabetes insipidus. J Am Soc Nephrol (1999) 1.33
Binding and transfer of verocytotoxin by polymorphonuclear leukocytes in hemolytic uremic syndrome. Blood (2000) 1.31
Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene. Am J Hum Genet (1994) 1.30
Genetic variability of herpes simplex virus: development of a pathogenic variant during passaging of a nonpathogenic herpes simplex virus type 1 virus strain in mouse brain. J Virol (1983) 1.27
Ceftriaxone-associated nephrolithiasis and biliary pseudolithiasis. Eur J Pediatr (1999) 1.22
Benign familial hematuria due to mutation of the type IV collagen alpha4 gene. J Clin Invest (1996) 1.22
Amplification of a short nucleotide sequence in the repeat units of defective herpes simplex virus type 1 Angelotti DNA. J Virol (1981) 1.21
Agrin is a major heparan sulfate proteoglycan in the human glomerular basement membrane. J Histochem Cytochem (1998) 1.20
Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis--a review. Eur J Pediatr (2009) 1.19
Haemolytic-uraemic syndrome. Epidemiological and clinical study. Arch Dis Child (1974) 1.19
Replacement of glycoprotein B gene sequences in herpes simplex virus type 1 strain ANG by corresponding sequences of the strain KOS causes changes of plaque morphology and neuropathogenicity. J Gen Virol (1987) 1.18
Experimental infection of inbred mice with herpes simplex virus. V. Investigations with a virus strain non-lethal after peripheral infection. J Gen Virol (1982) 1.18
Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue. Pediatrics (1977) 1.18
Precore-mediated inhibition of hepatitis B virus progeny DNA synthesis. J Virol (1993) 1.18
Monocyte chemoattractant protein-1 and interleukin-8 levels in urine and serum of patents with hemolytic uremic syndrome. Pediatr Res (1998) 1.17
RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems. Hum Mutat (2000) 1.17
A herpes simplex virus type 1 mutant with a deletion in the polypeptide-coding sequences of the ICP4 gene. J Gen Virol (1985) 1.16
Synthesis and packaging of herpes simplex virus DNA in the course of virus passages at high multiplicity. Intervirology (1978) 1.16
The clinical spectrum of type IV collagen mutations. Hum Mutat (1997) 1.16
Biochemical studies in the liver and muscle of patients with Zellweger syndrome. Pediatr Res (1983) 1.13
Hepatitis B virus genome is organized into nucleosomes in the nucleus of the infected cell. Virus Genes (1994) 1.13
Prognosis of extrahepatic biliary atresia. Arch Dis Child (1989) 1.12
Multidisciplinary behavioral treatment of defecation problems: a controlled study in children with anorectal malformations. J Pediatr Surg (2001) 1.09
The beneficial, antimicrobial effect of probiotics. Med Hypotheses (2001) 1.09
Verocytotoxin-producing Escherichia coli infection in hemolytic uremic syndrome in part of western Europe. Eur J Pediatr (1996) 1.07
New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels. J Am Soc Nephrol (1997) 1.05
Possible role of adenosine cyclic 3':5'-monophosphate phosphodiesterase in the morphological transformation of Chinese hamster ovary cells mediated by N6,O2-dibutyryl adenosine cyclic 3':5"-monophosphate. J Biol Chem (1975) 1.04
Replication of hepatitis B virus in a hepatocellular carcinoma. Virology (1990) 1.03
Replication of bacteriophage phichi174 replicative form DNA in vivo. J Mol Biol (1972) 1.03
Detection of verocytotoxin bound to circulating polymorphonuclear leukocytes of patients with hemolytic uremic syndrome. J Am Soc Nephrol (2001) 1.03
The molecular basis of Dutch infantile nephropathic cystinosis. Nephron (2001) 1.02
Experimental infection of inbred mice with herpes simplex virus. II. Interferon production and activation of natural killer cells in the peritoneal exudate. J Gen Virol (1981) 1.02
Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation. Kidney Int (2000) 1.00
Cognitive and psychosocial functioning of patients with congenital nephrogenic diabetes insipidus. Am J Med Genet (1996) 0.97
Defective replication units of hepatitis B virus. J Virol (1990) 0.96
Additional congenital defects in anorectal malformations. Eur J Pediatr (1996) 0.96
Persistent arterial hypotension after bilateral nephrectomy in a 4-month-old infant. Pediatr Nephrol (2001) 0.95
Plasma cytokine levels in hemolytic uremic syndrome. Nephron (1995) 0.95
Primary structure and high expression of human agrin in basement membranes of adult lung and kidney. Eur J Biochem (1998) 0.95
Low-renin, low-aldosterone hypertension and abnormal cortisol metabolism in a 19-month-old child. Horm Res (1982) 0.95
Rickets in a preterm infant during intravenous alimentation. Acta Paediatr Scand (1983) 0.94
Sequence of a replication competent hepatitis B virus genome with a preX open reading frame. Nucleic Acids Res (1990) 0.94
Coexistence of nucleosomal and various non-nucleosomal chromatin configurations in cells infected with herpes simplex virus. Eur J Cell Biol (1980) 0.93
Isolation and partial characterization of heparan sulphate proteoglycan from the human glomerular basement membrane. Biochem J (1989) 0.93
Children with chronic renal failure have reduced numbers of memory B cells. Clin Exp Immunol (2004) 0.92
The development of anti-glomerular basement membrane nephritis in two children with Alport's syndrome after renal transplantation: characterization of the antibody target. Pediatr Nephrol (1989) 0.91
Serological evidence for expression of the polymerase gene of human hepatitis B virus in vivo. J Gen Virol (1988) 0.91
The hepatocyte growth factor receptor kinase-mediated phosphorylation of lipocortin-1 transduces the proliferating signal of the hepatocyte growth factor. J Biol Chem (1996) 0.91
Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome. Clin Chim Acta (1987) 0.91
Aberrant splicing of the COL4A5 gene in patients with Alport syndrome. Hum Mol Genet (1994) 0.91
Mouse monoclonal antibody directed against hepatitis B virus X protein synthesized in Escherichia coli: detection of reactive antigen in liver cell carcinoma and chronic hepatitis. Oncology (1990) 0.90
Renal transplantation in 20 children with hemolytic-uremic syndrome. Clin Nephrol (1990) 0.90
Treatment of hyperhomocysteinemia in children on dialysis by folic acid. Pediatr Nephrol (1999) 0.89
The cognitive development of pre-school children treated for chronic renal failure. Pediatr Nephrol (1995) 0.89
Reversible deficient prostacyclin release in childhood hemolytic uremic syndrome. Int J Pediatr Nephrol (1982) 0.89
Herpes simplex virus type 1-induced interferon production and activation of natural killer cells in mice. J Gen Virol (1983) 0.89
Role of bacteria in the pathogenesis of short bowel syndrome-associated D-lactic acidemia. Microb Pathog (1997) 0.89
Hudrolysis of butyryl derivatives of adenosine cyclic 3':5'-monophosphate by Chinese hamster ovary cell extracts and characterization fo the products. J Biol Chem (1975) 0.89