Langheim S - Search Results

1

Erdheim-Chester disease: report on a case and new insights on its immunopathogenesis.

Dagna L, Girlanda S, Langheim S, Rizzo N, Bozzolo EP, Sabbadini MG, Ferrarini M. Dagna L, et al. Among authors: langheim s. Rheumatology (Oxford). 2010 Jun;49(6):1203-6. doi: 10.1093/rheumatology/kep461. Epub 2010 Jan 22. Rheumatology (Oxford). 2010. PMID: 20097905 No abstract available.

2

Tumor necrosis factor α as a master regulator of inflammation in Erdheim-Chester disease: rationale for the treatment of patients with infliximab.

Dagna L, Corti A, Langheim S, Guglielmi B, De Cobelli F, Doglioni C, Fragasso G, Sabbadini MG, Ferrarini M. Dagna L, et al. Among authors: langheim s. J Clin Oncol. 2012 Oct 1;30(28):e286-90. doi: 10.1200/JCO.2012.41.9911. Epub 2012 Aug 6. J Clin Oncol. 2012. PMID: 22869874 No abstract available.

3

Increased expression and secretion of resistin in epicardial adipose tissue of patients with acute coronary syndrome.

Langheim S, Dreas L, Veschini L, Maisano F, Foglieni C, Ferrarello S, Sinagra G, Zingone B, Alfieri O, Ferrero E, Maseri A, Ruotolo G. Langheim S, et al. Am J Physiol Heart Circ Physiol. 2010 Mar;298(3):H746-53. doi: 10.1152/ajpheart.00617.2009. Epub 2010 Jan 8. Am J Physiol Heart Circ Physiol. 2010. PMID: 20061546 Free article.

4

ABCG5 and ABCG8 require MDR2 for secretion of cholesterol into bile.

Langheim S, Yu L, von Bergmann K, Lütjohann D, Xu F, Hobbs HH, Cohen JC. Langheim S, et al. J Lipid Res. 2005 Aug;46(8):1732-8. doi: 10.1194/jlr.M500115-JLR200. Epub 2005 Jun 1. J Lipid Res. 2005. PMID: 15930516 Free article.

5

Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia.

Bertolini S, Pisciotta L, Di Scala L, Langheim S, Bellocchio A, Masturzo P, Cantafora A, Martini S, Averna M, Pes G, Stefanutti C, Calandra S. Bertolini S, et al. Among authors: langheim s. Atherosclerosis. 2004 May;174(1):57-65. doi: 10.1016/j.atherosclerosis.2003.12.037. Atherosclerosis. 2004. PMID: 15135251

6

Investigation into the role of apolipoprotein B gene 8344C/T variant on plasma cholesterol levels by allele-specific PCR amplification.

Cantafora A, Bertolini S, Blotta I, Rivabene R, Pisciotta L, Langheim S, Calandra S. Cantafora A, et al. Among authors: langheim s. Ann Ist Super Sanita. 2002;38(4):411-8. Ann Ist Super Sanita. 2002. PMID: 12760338

7

A "de novo" mutation of the LDL-receptor gene as the cause of familial hypercholesterolemia.

Pisciotta L, Cantafora A, De Stefano F, Langheim S, Calandra S, Bertolini S. Pisciotta L, et al. Among authors: langheim s. Biochim Biophys Acta. 2002 May 21;1587(1):7-11. doi: 10.1016/s0925-4439(02)00047-9. Biochim Biophys Acta. 2002. PMID: 12009418 Free article.

8

Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype.

Bertolini S, Cantafora A, Averna M, Cortese C, Motti C, Martini S, Pes G, Postiglione A, Stefanutti C, Blotta I, Pisciotta L, Rolleri M, Langheim S, Ghisellini M, Rabbone I, Calandra S. Bertolini S, et al. Among authors: langheim s. Arterioscler Thromb Vasc Biol. 2000 Sep;20(9):E41-52. doi: 10.1161/01.atv.20.9.e41. Arterioscler Thromb Vasc Biol. 2000. PMID: 10978268

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