Erknet

Erknet company information, Employees & Contact Information

Explore related pages

Related company profiles:

ERKNet, the European Reference Network for Rare Kidney Diseases, is a collaborative alliance of 72 specialized pediatric and adult nephrology centers in 24 European countries. Our main mission is to provide comprehensive medical care to a large community of over 70,000 patients with rare kidney diseases. Members of our network are committed to providing the highest level of multidisciplinary care for a broad spectrum of rare kidney diseases. They consistently adhere to clinical guidelines and protocols based on the latest medical advances, while ensuring rigorous monitoring of treatment quality and outcomes across the network. Beyond our clinical efforts, ERKNet is dedicated to improving knowledge about rare kidney disease, both among patients and healthcare professionals. We accomplish this by disseminating information about the disease through our website and a number of educational and training initiatives. To meet the needs of our patients, our network works closely with European patient advocacy groups (ePAGs) and various kidney patient communities and organizations. In addition, ERKNet plays an active role in supporting clinical research aimed at refining diagnosis, predicting risks, and advancing the development of new therapies for people with rare kidney disease.
Looking for a particular Erknet employee's phone or email?

Erknet Questions

News

Screening of mtr-miR156a from exosomes of dairy cow blood to milk and its regulatory effect on milk protein synthesis in BMECs - BMC Genomics

Screening of mtr-miR156a from exosomes of dairy cow blood to milk and its regulatory effect on milk protein synthesis in BMECs BMC Genomics

John Muir Trail Day 10: The Biggest Jerk at MTR - The Trek

John Muir Trail Day 10: The Biggest Jerk at MTR The Trek

Electron transfer via the non-Mtr respiratory pathway from Shewanella putrefaciens CN-32 for methyl orange bioreduction - ScienceDirect.com

Electron transfer via the non-Mtr respiratory pathway from Shewanella putrefaciens CN-32 for methyl orange bioreduction ScienceDirect.com

Saylor Hawkins - Swimming and Diving - University of North Texas Athletics

Saylor Hawkins - Swimming and Diving University of North Texas Athletics

“Association of MTHFR and MS/MTR gene polymorphisms with congenital heart defects in North Indian population (Jammu and Kashmir): a case–control study encompassing meta-analysis and trial sequential analysis” - BMC Pediatrics

“Association of MTHFR and MS/MTR gene polymorphisms with congenital heart defects in North Indian population (Jammu and Kashmir): a case–control study encompassing meta-analysis and trial sequential analysis” BMC Pediatrics

A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells development and retinal metabolism - Clinical Epigenetics

A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells development and retinal metabolism Clinical Epigenetics

Top Erknet Employees

Free Chrome Extension

Find emails, phones & company data instantly

Find verified emails from LinkedIn profiles
Get direct phone numbers & mobile contacts
Access company data & employee information
Works directly on LinkedIn - no copy/paste needed
Get Chrome Extension - Free

Aero Online

Your AI prospecting assistant