Diagnosis and Management of Inherited Kidney Diseases: What´s New?
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