6 papers found
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1
Fainting Fanconi syndrome clarified by proxy: a case report
Membranous nephropathy: a retrospective observational study of membranous nephropathy in north east and central London
Genetic, pathophysiological, and clinical aspects of nephrocalcinosis
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