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Last Updated: 11/29/2022

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Found 9 publications

10-Year Comparative Follow-up of Familial versus Multifactorial Chylomicronemia Syndromes.

Familial chylomicronemia syndrome due to a heterozygous deletion of the chromosome 8 treated with the apoCIII inhibitor volanesorsen: A case report.

THE PREVALENCE OF PROBABLE FAMILIAL CHYLOMICRONEMIA SYNDROME IN A SOUTHERN CALIFORNIA POPULATION.

Volanesorsen in the Treatment of Familial Chylomicronemia Syndrome or Hypertriglyceridaemia: Design, Development and Place in Therapy.

Case report of one month and 15 days old baby with type V hyperlipoproteinemia (HLP).

Familial chylomicronemia syndrome: an under-recognized cause of severe hypertriglyceridaemia.

The effect of volanesorsen treatment on the burden associated with familial chylomicronemia syndrome: the results of the ReFOCUS study.

Orlistat Therapy for Children With Type 1 Hyperlipoproteinemia: A Randomized Clinical Trial.

Showing 1-9 of 9

Last Updated: 11/29/2022