TARUGI P

Last name: TARUGI P

2003 (v1)

Publication

Metadata-only

Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency.

PISCIOTTA, LIVIA Miccoli R Cantafora A

No description

Uploaded on: April 14, 2023
2006 (v1)

Publication

Metadata-only

A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia.

Priore Oliva C Tarugi P Calandra S

No description

Uploaded on: April 14, 2023
2011 (v1)

Publication

Metadata-only

Hypoalpha-hypobetalipoproteinemia (Familial Combined Hypolipidemia) caused by loss of function mutations of ANGPTL3 gene.

Pisciotta L Di Leo E Tarugi P

No description

Uploaded on: May 13, 2023
2004 (v1)

Publication

Metadata-only

Beta-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia.

Calandra S BERTOLINI, STEFANO Pes GM

No description

Uploaded on: April 14, 2023
2004 (v1)

Publication

Metadata-only

Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders.

PISCIOTTA, LIVIA BERTOLINI, STEFANO Hamilton Craig I

No description

Uploaded on: April 14, 2023
2011 (v1)

Publication

Metadata-only

Characterization of Three Kindred with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3.

PISCIOTTA, LIVIA BERTOLINI, STEFANO Favari E

Background—Angiopoietin-like protein 3 (ANGPTL3) affects lipid metabolism by inhibiting the activity of lipoprotein and endothelial lipases. Angptl3 knockout mice have marked hypolipidemia, and heterozygous carriers of ANGPLT3, loss-of-function mutations were found among individuals in the lowest quartile of plasma triglycerides in...

Uploaded on: March 27, 2023

TARUGI P

Recent uploads