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Unilateral multicystic dysplastic kidney: experience in children

BJU international, 2004-02, Vol.93 (3), p.388-392

2004

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Activation of the AKT/mTOR pathway in autosomal recessive polycystic kidney disease (ARPKD)

Nephrology, dialysis, transplantation, 2009-06, Vol.24 (6), p.1819-1827

2009

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Recurrence of severe steroid dependency in cyclosporin A-treated childhood idiopathic nephrotic syndrome

Nephrology, dialysis, transplantation, 2004-05, Vol.19 (5), p.1136-1141

2004

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Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

Journal of the American Society of Nephrology, 2001-09, Vol.12 (9), p.1872-1881

2001

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Central nervous system involvement in hemolytic uremic syndrome (HUS)--a retrospective analysis of cerebral CT and MRI studies

Clinical nephrology, 2001-12, Vol.56 (6), p.S3

2001

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Familial hypomagnesemia-hypercalciuria in 2 siblings

Clinical nephrology, 2001-08, Vol.56 (2), p.155

2001

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Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations

Kidney international, 1998-06, Vol.53 (6), p.1594-1600

1998

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Need for Long-term Follow-up in Enterohemorrhagic Escherichia coli—Associated Hemolytic Uremic Syndrome Due to Late-Emerging Sequelae

Clinical infectious diseases, 2012-05, Vol.54 (10), p.1413-1421

2012

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Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome

Journal of the American Society of Nephrology, 2008-02, Vol.19 (2), p.365-371

2008

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Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

Kidney international, 2005-03, Vol.67 (3), p.829-848

2005

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High prevalence of febrile urinary tract infections after paediatric renal transplantation

Nephrology, dialysis, transplantation, 2006-11, Vol.21 (11), p.3269-3274

2006

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Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Nephrology, dialysis, transplantation, 2008-11, Vol.23 (11), p.3527-3533

2008

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Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender

Acta Paediatrica, 1996-04, Vol.85 (4), p.437-445

1996

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Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. Commentary

Kidney international, 2006, Vol.70 (6)

2006

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Clinical features of unilateral multicystic renal dysplasia in children

European journal of pediatrics, 1998-08, Vol.157 (8), p.666-672

1998

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Novel OCRL1 Mutations in Patients With the Phenotype of Dent Disease

American journal of kidney diseases, 2006-12, Vol.48 (6), p.942.e1-942.e14

2006

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Metabolic effects of long-term growth hormone treatment in prepubertal children with chronic renal failure and after kidney transplantation

Pediatric research, 1998-02, Vol.43 (2), p.209-215

1998

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Unilateral multicystic dysplastic kidney: experience in children

Activation of the AKT/mTOR pathway in autosomal recessive polycystic kidney disease (ARPKD)

Recurrence of severe steroid dependency in cyclosporin A-treated childhood idiopathic nephrotic syndrome

Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

Central nervous system involvement in hemolytic uremic syndrome (HUS)--a retrospective analysis of cerebral CT and MRI studies

Familial hypomagnesemia-hypercalciuria in 2 siblings

Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations

Need for Long-term Follow-up in Enterohemorrhagic Escherichia coli—Associated Hemolytic Uremic Syndrome Due to Late-Emerging Sequelae

Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome

Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

High prevalence of febrile urinary tract infections after paediatric renal transplantation

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. Commentary

Clinical features of unilateral multicystic renal dysplasia in children

Novel OCRL1 Mutations in Patients With the Phenotype of Dent Disease

Metabolic effects of long-term growth hormone treatment in prepubertal children with chronic renal failure and after kidney transplantation

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