University of Leicester
Leicester, United Kingdom
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What is new in IgA nephropathy research, which clinical trials are open, and who works on it. From public registries and PubMed, with the source and date of every fact.
The trial team decides who can take part; your doctor can help you ask.
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Results, new trials and publications, newest first. Every item links to its source.
Results and new studies, newest first, in plain words.
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Publication
Journal of inflammation research
PubMed · PMID 42979491Publication
Frontiers in bioscience (Landmark edition)
PubMed · PMID 42980025Case report
BMC pediatrics
PubMed · PMID 42983718Helplines, patient groups and support services for you and your family.
Federation of national kidney patient organisations: information materials, webinars, annual summit, youth camp, EU advocacy.
Visit site: European Kidney Patients' FederationUmbrella of European patient organisations and national patient coalitions.
Visit site: European Patients' Forum (EPF)Alliance of over 1,000 rare disease patient organisations, with a list of rare disease helplines by country.
Visit site: EURORDIS – Rare Diseases EuropePatient-run IgAN non-profit (US-based, 'Go Global Network'): education, provider finder, patient registry, app, patient aid, research and clinical trial information.
Visit site: IgA Nephropathy FoundationGlobal alliance of patient organisations of all diseases, promoting patient-centred healthcare.
Visit site: International Alliance of Patients' OrganizationsFrontlight is not affiliated with these organisations; we list them because they help.
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Groups with active IgA nephropathy work.
Leicester, United Kingdom
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Beijing, China
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Tokyo, Japan
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Beijing, China
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Stanford, United States
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Birmingham, United States
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Tokyo, Japan
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Hangzhou, China
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Stanford, United States
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Shanghai, China
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Vancouver, Canada
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Sydney, Australia
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