English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Lipoprotein lipase (LPL) deficiency is a rare autosomal recessive disorder caused by LPL gene mutation and is characterized by severe hyperchylomicronemia. Patients with LPL deficiency suffer from the frequent recurrence of acute pancreatitis, but the underlying mechanisms are not fully understood.

the journal of clinical endocrinology and metabolism/journal of clinical endocrinology and metabolism

Long-Term Course of Lipoprotein Lipase (LPL) Deficiency Due to Homozygous LPL<sub>Arita</sub>in a Patient with Recurrent Pancreatitis, Retained Glucose Tolerance, and Atherosclerosis

Long-Term Course of Lipoprotein Lipase (LPL) Deficiency Due to Homozygous LPLAritain a Patient with Recurrent Pancreatitis, Retained Glucose Tolerance, and Atherosclerosis

Long-Term Course of Lipoprotein Lipase (LPL) Deficiency Due to Homozygous LPL_Aritain a Patient with Recurrent Pancreatitis, Retained Glucose Tolerance, and Atherosclerosis