News
Just published in Kidney International Reports | Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions
Discover groundbreaking insights into how HNF1B variants impact kidney survival in patients with chronic kidney disease.
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Just published in European Journal of Human Genetics | Consensus Statement on Bardet-Biedl Syndrome
Joint effort by ERN-Eye, ERKNet, Endo-ERN, and ERN-ITHACA!
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Just published in Atherosclerosis| CPR on lipoprotein apheresis for children with homozygous familial hypercholesterolaemia
An expert consensus statement from ERKNet and ESPN
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Just published in Nature Reviews Nephrology! CPR for kidney involvement in tuberous sclerosis complex
A joint effort of ERKNet and ERA on providing a global overview on the management of TSC-associated kidney disease!
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Follow ERKNet on social media!
Exciting times ahead as we unveil our redesigned social media presence tomorrow!
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Review on childhood nephrotic syndrome published in the Lancet
Don't miss taking a look at the very interesting article which is available online for free until October 20!
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ERKNet Summer Newsletter 2023
Find interesting and exciting updates on our network and its activities in this year's summer newsletter.
Have a nice summer holiday!
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20,000th patient in ERKReg enrolled
Important milestone achieved - thanks to all ERKReg editors!
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We would like to introduce ourselves!
ERKNet is revolutionizing Rare Kidney Disease Care in Europe!
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