Bertelli M - Search Results

1

Improvement of quality of life by intake of hydroxytyrosol in patients with lymphedema and association of lymphedema genes with obesity.

Dhuli K, Ceccarini MR, Precone V, Maltese PE, Bonetti G, Paolacci S, Dautaj A, Guerri G, Marceddu G, Beccari T, Michelini S, Bertelli M. Dhuli K, et al. Among authors: bertelli m. Eur Rev Med Pharmacol Sci. 2021 Dec;25(1 Suppl):33-42. doi: 10.26355/eurrev_202112_27331. Eur Rev Med Pharmacol Sci. 2021. PMID: 34890032 Free article.

2

Clinical and genetic study of 46 Italian patients with primary lymphedema.

Michelini S, Degiorgio D, Cestari M, Corda D, Ricci M, Cardone M, Mander A, Famoso L, Contini E, Serrani R, Pinelli L, Cecchin S, Bertelli M. Michelini S, et al. Among authors: bertelli m. Lymphology. 2012 Mar;45(1):3-12. Lymphology. 2012. PMID: 22768468

3

Polymorphisms of alpha-actinin-3 and ciliary neurotrophic factor in national-level Italian athletes.

Persi A, Maltese PE, Bertelli M, Cecchin S, Ciaghi M, Guarnieri MC, Agnello L, Maggioni MA, Merati G, Veicsteinas A. Persi A, et al. Among authors: bertelli m. Panminerva Med. 2013 Jun;55(2):217-24. Panminerva Med. 2013. PMID: 23676962

4

Choroidal Thickness Analysis in Patients with Usher Syndrome Type 2 Using EDI OCT.

Colombo L, Sala B, Montesano G, Pierrottet C, De Cillà S, Maltese P, Bertelli M, Rossetti L. Colombo L, et al. Among authors: bertelli m. J Ophthalmol. 2015;2015:189140. doi: 10.1155/2015/189140. Epub 2015 May 17. J Ophthalmol. 2015. PMID: 26075083 Free PMC article.

5

Polymorphism of UGT1A1*28 (TA)7 and liver damage in hepatitis B virus-positive patients in Albania.

Marku E, Maltese PE, Koni M, Capodicasa N, Qendro IS, Rigoni E, Cecchin S, Bertelli M. Marku E, et al. Among authors: bertelli m. Genet Mol Res. 2015 May 18;14(2):5221-8. doi: 10.4238/2015.May.18.13. Genet Mol Res. 2015. PMID: 26125716 Free article.

6

Genetic polymorphisms and retinal vein occlusion in an Italian population.

De Polo L, Maltese PE, Rigoni E, Bertelli M, Cecchin S, Staurenghi G, Stoppa G. De Polo L, et al. Among authors: bertelli m. Genet Mol Res. 2015 Oct 27;14(4):13337-41. doi: 10.4238/2015.October.26.30. Genet Mol Res. 2015. PMID: 26535647 Free article.

7

FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein function.

Tavian D, Missaglia S, Maltese PE, Michelini S, Fiorentino A, Ricci M, Serrani R, Walter MA, Bertelli M. Tavian D, et al. Among authors: bertelli m. Oncotarget. 2016 Aug 23;7(34):54228-54239. doi: 10.18632/oncotarget.9797. Oncotarget. 2016. PMID: 27276711 Free PMC article.

8

Genetic evaluation of AMPD1, CPT2, and PGYM metabolic enzymes in patients with chronic fatigue syndrome.

Maltese PE, Venturini L, Poplavskaya E, Bertelli M, Cecchin S, Granato M, Nikulina SY, Salmina A, Aksyutina N, Capelli E, Ricevuti G, Lorusso L. Maltese PE, et al. Among authors: bertelli m. Genet Mol Res. 2016 Jul 29;15(3). doi: 10.4238/gmr.15038717. Genet Mol Res. 2016. PMID: 27525900 Free article.

9

Prevalence of mutations in LEP, LEPR, and MC4R genes in individuals with severe obesity.

Paolini B, Maltese PE, Del Ciondolo I, Tavian D, Missaglia S, Ciuoli C, Zuntini M, Cecchin S, Bertelli M, Pompucci G. Paolini B, et al. Among authors: bertelli m. Genet Mol Res. 2016 Aug 19;15(3). doi: 10.4238/gmr.15038718. Genet Mol Res. 2016. PMID: 27706562 Free article.

10

Gene-Targeted Analysis of Clinically Diagnosed Long QT Russian Families.

Maltese PE, Orlova N, Krasikova E, Emelyanchik E, Cheremisina A, Kuscaeva A, Salmina A, Miotto R, Bonizzato A, Guerri G, Zuntini M, Nicoulina S, Bertelli M. Maltese PE, et al. Among authors: bertelli m. Int Heart J. 2017 Feb 7;58(1):81-87. doi: 10.1536/ihj.16-133. Epub 2016 Dec 21. Int Heart J. 2017. PMID: 28003625 Free article.

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