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Renal tubular function in children with tyrosinaemia type I treated with nitisinone

Journal of inherited metabolic disease, 2008-06, Vol.31 (3), p.399-402

2008

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Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment

Nephrology, dialysis, transplantation, 2012-05, Vol.27 (5), p.1729-1736

2012

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Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

Journal of medical genetics, 2002-11, Vol.39 (11), p.796-803

2002

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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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Evaluation of urinary tract calculi in children

Archives of disease in childhood, 2001-04, Vol.84 (4), p.320-323

Hulton, S-A

2001

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Antenatal diagnosis of fetal renal calculus

Ultrasound in obstetrics & gynecology, 2005-05, Vol.25 (5), p.517-518

2005

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Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing ( rdRTA2 ) to 7q33-34

American journal of human genetics, 1999-12, Vol.65 (6), p.1656-1665

1999

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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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Hypertension: a cause of growth impairment

Journal of human hypertension, 2002-05, Vol.16 (5), p.363-366

2002

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Care in the use of ibuprofen as an antipyretic in children

Clinical nephrology, 1998-05, Vol.49 (5), p.293

1998

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Plasma oxalate and eGFR are correlated in primary hyperoxaluria patients with maintained kidney function—data from three placebo-controlled studies

Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.1785-1793

2021

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Cyclosporin-related nephrotoxicity in children with nephrotic syndrome

Pediatric nephrology (Berlin, West), 2002-03, Vol.17 (3), p.225-226

2002

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Combined liver–kidney transplantation for primary hyperoxaluria type 1 in young children

Nephrology, dialysis, transplantation, 2001-02, Vol.16 (2), p.348-354

2001

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Lymphocyte subpopulations, interleukin-2 and interleukin-2 receptor expression in childhood nephrotic syndrome

Pediatric nephrology (Berlin, West), 1994-04, Vol.8 (2), p.135-139

1994

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Efficacy and safety of Oxalobacter formigenes to reduce urinary oxalate in primary hyperoxaluria

Nephrology, dialysis, transplantation, 2011-11, Vol.26 (11), p.3609-3615

2011

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The prevalence and treatment of end-stage renal disease in an Asian child population

Nephrology, dialysis, transplantation, 1997-12, Vol.12 (12), p.2517-2520

1997

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A case of neonatal Bartter's syndrome

Pediatric nephrology (Berlin, West), 1996-08, Vol.10 (4), p.414-418

1996

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Vincristine and focal segmental sclerosis : do we need a multicentre trial?

Pediatric nephrology (Berlin, West), 1998-05, Vol.12 (4), p.284-289

1998

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Urinary l-lactate excretion is increased in renal Fanconi syndrome

Nephrology, dialysis, transplantation, 2004-07, Vol.19 (7), p.1767-1773

2004

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Characteristics and Outcomes of Children with Primary Oxalosis Requiring Renal Replacement Therapy

Clinical journal of the American Society of Nephrology, 2012-03, Vol.7 (3), p.458-465

2012

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Pre-emptive liver transplantation for primary hyperoxaluria (PH-I) arrests long-term renal function deterioration

Nephrology, dialysis, transplantation, 2011, Vol.26 (1), p.354-359

2011

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Long-term cyclosporin A treatment of minimal-change nephrotic syndrome of childhood

Pediatric nephrology (Berlin, West), 1994-08, Vol.8 (4), p.401-403

1994

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Hypertension: a cause of growth impairment

Journal of human hypertension, 2002-05, Vol.16 (5), p.363

2002

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Tubular proteinuria in steroid sensitive multi-relapsing nephrotic syndrome

Clinical nephrology, 1993-07, Vol.40 (1), p.26

1993

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Renal tubular function in children with tyrosinaemia type I treated with nitisinone

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment

Mutations in the gene encoding B1 subunit of H + -ATPase cause renal tubular acidosis with sensorineural deafness

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

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

Evaluation of urinary tract calculi in children

Antenatal diagnosis of fetal renal calculus

Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing ( rdRTA2 ) to 7q33-34

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

Hypertension: a cause of growth impairment

Care in the use of ibuprofen as an antipyretic in children

Plasma oxalate and eGFR are correlated in primary hyperoxaluria patients with maintained kidney function—data from three placebo-controlled studies

Cyclosporin-related nephrotoxicity in children with nephrotic syndrome

Combined liver–kidney transplantation for primary hyperoxaluria type 1 in young children

Lymphocyte subpopulations, interleukin-2 and interleukin-2 receptor expression in childhood nephrotic syndrome

Efficacy and safety of Oxalobacter formigenes to reduce urinary oxalate in primary hyperoxaluria

The prevalence and treatment of end-stage renal disease in an Asian child population

A case of neonatal Bartter's syndrome

Vincristine and focal segmental sclerosis : do we need a multicentre trial?

Urinary l-lactate excretion is increased in renal Fanconi syndrome

Characteristics and Outcomes of Children with Primary Oxalosis Requiring Renal Replacement Therapy

Pre-emptive liver transplantation for primary hyperoxaluria (PH-I) arrests long-term renal function deterioration

Long-term cyclosporin A treatment of minimal-change nephrotic syndrome of childhood

Hypertension: a cause of growth impairment

Tubular proteinuria in steroid sensitive multi-relapsing nephrotic syndrome

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