Tarugi P - Search Results

1

A novel APOB mutation identified by exome sequencing cosegregates with steatosis, liver cancer, and hypocholesterolemia.

Cefalù AB, Pirruccello JP, Noto D, Gabriel S, Valenti V, Gupta N, Spina R, Tarugi P, Kathiresan S, Averna MR. Cefalù AB, et al. Among authors: tarugi p. Arterioscler Thromb Vasc Biol. 2013 Aug;33(8):2021-5. doi: 10.1161/ATVBAHA.112.301101. Epub 2013 May 30. Arterioscler Thromb Vasc Biol. 2013. PMID: 23723369 Free PMC article.

2

Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B.

Tarugi P, Lonardo A, Ballarini G, Grisendi A, Pulvirenti M, Bagni A, Calandra S. Tarugi P, et al. Gastroenterology. 1996 Oct;111(4):1125-33. doi: 10.1016/s0016-5085(96)70082-3. Gastroenterology. 1996. PMID: 8831609

3

A study of fatty liver disease and plasma lipoproteins in a kindred with familial hypobetalipoproteinemia due to a novel truncated form of apolipoprotein B (APO B-54.5).

Tarugi P, Lonardo A, Ballarini G, Erspamer L, Tondelli E, Bertolini S, Calandra S. Tarugi P, et al. J Hepatol. 2000 Sep;33(3):361-70. doi: 10.1016/s0168-8278(00)80270-6. J Hepatol. 2000. PMID: 11019990

4

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

Pisciotta L, Hamilton-Craig I, Tarugi P, Bellocchio A, Fasano T, Alessandrini P, Bon GB, Siepi D, Mannarino E, Cattin L, Averna M, Cefalù AB, Cantafora A, Calandra S, Bertolini S. Pisciotta L, et al. Among authors: tarugi p. Atherosclerosis. 2004 Feb;172(2):309-20. doi: 10.1016/j.atherosclerosis.2003.11.009. Atherosclerosis. 2004. PMID: 15019541

5

Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia.

Di Leo E, Lancellotti S, Penacchioni JY, Cefalù AB, Averna M, Pisciotta L, Bertolini S, Calandra S, Gabelli C, Tarugi P. Di Leo E, et al. Among authors: tarugi p. Atherosclerosis. 2005 Jun;180(2):311-8. doi: 10.1016/j.atherosclerosis.2004.12.004. Epub 2005 Jan 19. Atherosclerosis. 2005. PMID: 15910857

6

Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia.

Pisciotta L, Priore Oliva C, Cefalù AB, Noto D, Bellocchio A, Fresa R, Cantafora A, Patel D, Averna M, Tarugi P, Calandra S, Bertolini S. Pisciotta L, et al. Among authors: tarugi p. Atherosclerosis. 2006 Jun;186(2):433-40. doi: 10.1016/j.atherosclerosis.2005.08.015. Epub 2005 Sep 23. Atherosclerosis. 2006. PMID: 16183066

7

A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol.

Fasano T, Cefalù AB, Di Leo E, Noto D, Pollaccia D, Bocchi L, Valenti V, Bonardi R, Guardamagna O, Averna M, Tarugi P. Fasano T, et al. Among authors: tarugi p. Arterioscler Thromb Vasc Biol. 2007 Mar;27(3):677-81. doi: 10.1161/01.ATV.0000255311.26383.2f. Epub 2006 Dec 14. Arterioscler Thromb Vasc Biol. 2007. PMID: 17170371

8

Molecular diagnosis of hypobetalipoproteinemia: an ENID review.

Tarugi P, Averna M, Di Leo E, Cefalù AB, Noto D, Magnolo L, Cattin L, Bertolini S, Calandra S. Tarugi P, et al. Atherosclerosis. 2007 Dec;195(2):e19-27. doi: 10.1016/j.atherosclerosis.2007.05.003. Epub 2007 Jun 14. Atherosclerosis. 2007. PMID: 17570373 Review.

9

Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemia.

Cefalù AB, Noto D, Magnolo L, Pinotti E, Gomaraschi M, Martini S, Vigna GB, Calabresi L, Tarugi P, Averna MR. Cefalù AB, et al. Among authors: tarugi p. Atherosclerosis. 2009 May;204(1):202-7. doi: 10.1016/j.atherosclerosis.2008.08.031. Epub 2008 Sep 4. Atherosclerosis. 2009. PMID: 18926541

10

PCSK9 dominant negative mutant results in increased LDL catabolic rate and familial hypobetalipoproteinemia.

Cariou B, Ouguerram K, Zaïr Y, Guerois R, Langhi C, Kourimate S, Benoit I, Le May C, Gayet C, Belabbas K, Dufernez F, Chétiveaux M, Tarugi P, Krempf M, Benlian P, Costet P. Cariou B, et al. Among authors: tarugi p. Arterioscler Thromb Vasc Biol. 2009 Dec;29(12):2191-7. doi: 10.1161/ATVBAHA.109.194191. Epub 2009 Sep 17. Arterioscler Thromb Vasc Biol. 2009. PMID: 19762784

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