Background: Mutations in the LPL gene cause familial lipoprotein lipase deficiency. Symptoms of familial LPL deficiency usually begin in childhood and include abdominal pain, acute and recurrent ...

During the first 18 months after treatment with alipogene tiparvovec, a gene therapy recently approved in Europe to treat lipoprotein lipase deficiency (LPLD), the first patient to receive the ...

As in patients with GPIHBP1 deficiency, those with GPIHBP1 autoantibodies had low plasma levels of lipoprotein lipase. Three of the six patients had systemic lupus erythematosus.

During the first 18 months after treatment with ali-pogene tiparvovec, a gene therapy recently approved in Europe to treat lipoprotein lipase deficiency (LPLD), the first patient to receive the ...

26 Sep 2014. Researchers have connected the dots in a pivotal pathway that they believe may tip the balance toward Alzheimer’s disease. In a study published September 17 in Neuron, Guojun Bu at the ...

lipoprotein lipase deficiency, cell & molecular biology. Coronavirus Mutations Could Muddle COVID-19 PCR Tests. Jack J. Lee | May 17, 2021 | 4 min read. Researchers find that SARS-CoV-2 variants can ...

The lipoprotein (a) test — or Lp(a) test — determines the level of this lipoprotein in the blood, and its results are used to diagnose several diseases, especially those related to the heart.