News - lald.org

EASL Congress 2026: Barcelona at the heart of hepatology From May 26–29, Barcelona hosted the EASL Congress 2026, one of the leading...

LAL-D Patient Organization Joins CardioAlianza On May 20, 2026, during the General Assembly of CardioAlianza held in Valencia, the incorporation...

A new publication in Hepatology International provides important evidence about the role of lysosomal acid lipase (LAL) in liver disease...

The National Federation of Liver Patients and Transplant Recipients (FNETH), part of COCEMFE, is running in 2026 the project “Accede Público...

LAL‑D Study – Phase 3 the University of Rochester (USA) is currently conducting Phase 3 of its research project on Lysosomal Acid Lipase...

Genetic liver diseases: rare, but clinically highly relevant This article highlights that genetic liver diseases, while individually uncommon,...

en‑LISOS Journal – Issue No. 9, March 2026 en‑LISOS has published its Issue 9 (March 2026), featuring scientific and informative content focused...

12th Interdisciplinary Conference on Advances in Rare Diseases On March 6, we took part in the 12th Interdisciplinary Conference on Advances in...

Martina, affected by LAL-D, represented the LAL-D Patient Organization at the event On the occasion of World Rare Disease Day, the FC Barcelona...

Rare Liver Diseases take the spotlight at the European Parliament — and LAL-D Patient Organization was there On Rare Disease Day, our...

RARE DISEASE DAY 2026 February 28th marks Rare Disease Day. Early diagnosis can change a life. High cholesterol is very common in the population....

Grupo Alimentario Copese We are incredibly happy to share this news. 💜 Thanks to the outreach efforts of the people involved in our association,...