News - lald.org

United for Newborn Screening in Europe

LAL-D Patient Organization joins the European call to strengthen newborn screening and reduce inequalities across Europe LAL-D Patient...

FEETEG and LAL-D Patient Organization Renew Their Collaboration Agreement On September 3, 2026, the Spanish Foundation for the Study and...

New Research Identifies a Pathway Regulating Lysosomal Acid Lipase (LAL) Activity and Lysosomal Health Research into lysosomal diseases continues...

New Publication Expands Knowledge of Wolman Disease and Reports a Novel LIPA Variant A recent article published in Frontiers in Pediatrics...

New Research Project Explores Innovative Strategies for Lysosomal Acid Lipase Deficiency (LAL-D) At LAL-D Patient Organization, we would...

New International LAL-D Registry Study Shows Sustained Improvements in Lipid Profiles with Sebelipase Alfa Treatment A new study...

University of Rochester Seeks Participants for Final Validation Study of a New Lysosomal Acid Lipase Deficiency (LAL-D) Assessment Tool The...

LIPA c.894G>A: From Patients to Models A study recently accepted for publication in Scientific Reports describes the first mouse model...

“Lipids and Health” Conference: Early Diagnosis, Multidisciplinary Care and Access to Treatment [video width="1080" height="1080"...

“Lipids and Health” Conference Next June 30 at 5:00 p.m., Cardioalianza, LAL-D Patient Organization, ASCAHIFA and Asociación Síndrome...

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...