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Page 1
The variability of SMCHD1 gene in FSHD patients: evidence of new mutations.
Strafella C, Caputo V, Galota RM, Campoli G, Bax C, Colantoni L, Minozzi G, Orsini C, Politano L, Tasca G, Novelli G, Ricci E, Giardina E, Cascella R. Strafella C, et al. Among authors: giardina e. Hum Mol Genet. 2019 Dec 1;28(23):3912-3920. doi: 10.1093/hmg/ddz239. Hum Mol Genet. 2019. PMID: 31600781 Free PMC article.
Mapping a dominant form of multinodular goiter to chromosome Xp22.
Capon F, Tacconelli A, Giardina E, Sciacchitano S, Bruno R, Tassi V, Trischitta V, Filetti S, Dallapiccola B, Novelli G. Capon F, et al. Among authors: giardina e. Am J Hum Genet. 2000 Oct;67(4):1004-7. doi: 10.1086/303095. Epub 2000 Sep 11. Am J Hum Genet. 2000. PMID: 10986044 Free PMC article.
Role of genetics in prevention of coronary atherosclerosis.
Novelli G, Borgiani P, Giardina E, Mango R, Contino G, Romeo F, Mehta JL. Novelli G, et al. Among authors: giardina e. Curr Opin Cardiol. 2003 Sep;18(5):368-71. doi: 10.1097/00001573-200309000-00008. Curr Opin Cardiol. 2003. PMID: 12960469 Review.
The psoriasis genetics as a model of complex disease.
Giardina E, Sinibaldi C, Novelli G. Giardina E, et al. Curr Drug Targets Inflamm Allergy. 2004 Jun;3(2):129-36. doi: 10.2174/1568010043343877. Curr Drug Targets Inflamm Allergy. 2004. PMID: 15180465 Review.
314 results