HLA-B12 as a genetic marker for vesicoureteric reflux?

Significance of vesicoureteric reflux.

Vesicoureteric reflux and nephropathy.

Vesicoureteric reflux in children.

Reflux nephropathy secondary to intrauterine vesicoureteric reflux.

Vesicoureteric reflux in children.

Nephrotic syndrome in vesicoureteric reflux.

Nephrotic syndrome in vesicoureteric reflux.

Proteinuria and enzymuria in vesicoureteric reflux.

The management of vesicoureteric reflux in children.

Management of vesicoureteric reflux in children.

Correction of vesicoureteric reflux by endoscopic injection.

A gamma camera method for quantitation of split renal function in children followed for vesicoureteric reflux.

Symptom index as a marker of gastro-oesophageal reflux disease.

The long-term follow-up of surgically treated vesicoureteric reflux.

Vesicoureteric reflux and reflux nephropathy: from mouse models to childhood disease.

Vesicoureteric reflux and renal scars in asymptomatic siblings of children with reflux.

Atypical presentation of posterior reversible encephalopathy: in a child with bilateral grade IV vesicoureteric reflux.

Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux.

Management of urinary tract infection and vesicoureteric reflux in children. 2. The case for surgery.

A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development.

C4BQ0 as a marker of genetic predisposition to liver cirrhosis.

Lipoprotein (a): genetic marker for atherosclerosis?

Autoantibodies to Tamm-Horsfall protein in detection of vesicoureteric reflux and kidney scarring.

Renin and blood-pressure in children with renal scarring and vesicoureteric reflux.

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Significance of vesicoureteric reflux.

Vesicoureteric reflux and nephropathy.

Vesicoureteric reflux in children.

Reflux nephropathy secondary to intrauterine vesicoureteric reflux.

Vesicoureteric reflux in children.

Nephrotic syndrome in vesicoureteric reflux.

Nephrotic syndrome in vesicoureteric reflux.

Proteinuria and enzymuria in vesicoureteric reflux.

The management of vesicoureteric reflux in children.

Management of vesicoureteric reflux in children.

Correction of vesicoureteric reflux by endoscopic injection.

A gamma camera method for quantitation of split renal function in children followed for vesicoureteric reflux.

Symptom index as a marker of gastro-oesophageal reflux disease.

The long-term follow-up of surgically treated vesicoureteric reflux.

Vesicoureteric reflux and reflux nephropathy: from mouse models to childhood disease.

Vesicoureteric reflux and renal scars in asymptomatic siblings of children with reflux.

Atypical presentation of posterior reversible encephalopathy: in a child with bilateral grade IV vesicoureteric reflux.

Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux.

Management of urinary tract infection and vesicoureteric reflux in children. 2. The case for surgery.

A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development.

C4BQ0 as a marker of genetic predisposition to liver cirrhosis.

Lipoprotein (a): genetic marker for atherosclerosis?

Autoantibodies to Tamm-Horsfall protein in detection of vesicoureteric reflux and kidney scarring.

Renin and blood-pressure in children with renal scarring and vesicoureteric reflux.

HLA-B12 as a genetic marker for vesicoureteric reflux?

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