WGiKD CME Workshop held June 3, 2017, Madrid, Spain, on occasion of ERA-EDTA Annual Meeting

Collagen IV glomerulopathies: an underdiagnosed phenotypic chameleon?

Constantinos Deltas, Nicosia, Cyprus

Alport Syndrome: a treatable hereditary kidney disease

Oliver Gross, Göttingen, Germany

NGS podocytopathy panel screening in adults with CKD of unknown origin: findings from the GCKD study

Anna Koettgen, Freiburg, Germany

C3 glomerulopathy: role of complement for pathogenesis and treatment

Marina Vivarelli, Rome, Italy

Advances in molecular understanding of cystinosis: implications for therapy

Corinne Antignac, Paris, France

Preimplantation genetic diagnosis for inherited renal diseases

Nine V.A.M. Knoers, Utrecht, The Netherlands

The European Reference Network for Rare Kidney Diseases

Franz Schaefer, Heidelberg, Germany