Cecchin S - Search Results

1

Autoantibodies in patients with post-COVID syndrome: a possible link with severity?

Ceccarini MR, Bonetti G, Medori MC, Dhuli K, Tezzele S, Micheletti C, Maltese PE, Cecchin S, Donato K, Fioretti F, Calzoni A, Praderio A, De Angelis MG, Nodari S, Arabia G, Lorusso L, Beccari T, Bertelli M. Ceccarini MR, et al. Among authors: cecchin s. Eur Rev Med Pharmacol Sci. 2023 Dec;27(6 Suppl):48-56. doi: 10.26355/eurrev_202312_34689. Eur Rev Med Pharmacol Sci. 2023. PMID: 38112956 Free article.

2

Identification of a novel mutation in the spastin gene (SPG4) in an Italian family with hereditary spastic paresis.

Bertelli M, Cecchin S, Lorusso L, Sidoti V, Fabbri A, Lapucci C, Buda A, Pandolfo M. Bertelli M, et al. Among authors: cecchin s. Panminerva Med. 2006 Sep;48(3):193-7. Panminerva Med. 2006. PMID: 17122756

3

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: cecchin s. 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.

4

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: cecchin s. 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.

5

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: cecchin s. Genet Mol Res. 2016 Jul 29;15(3). doi: 10.4238/gmr.15038717. Genet Mol Res. 2016. PMID: 27525900 Free article.

6

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: cecchin s. Genet Mol Res. 2016 Aug 19;15(3). doi: 10.4238/gmr.15038718. Genet Mol Res. 2016. PMID: 27706562 Free article.

7

Genetic tests for low- and middle-income countries: a literature review.

Maltese PE, Poplavskaia E, Malyutkina I, Sirocco F, Bonizzato A, Capodicasa N, Nicoulina SY, Salmina A, Aksutina N, Dundar M, Beccari T, Cecchin S, Bertelli M. Maltese PE, et al. Among authors: cecchin s. Genet Mol Res. 2017 Feb 8;16(1). doi: 10.4238/gmr16019466. Genet Mol Res. 2017. PMID: 28198508 Free article. Review.

8

Hypothyroidism and hyperthyroidism.

Guerri G, Bressan S, Sartori M, Costantini A, Benedetti S, Agostini F, Tezzele S, Cecchin S, Scaramuzza A, Bertelli M. Guerri G, et al. Among authors: cecchin s. Acta Biomed. 2019 Sep 30;90(10-S):83-86. doi: 10.23750/abm.v90i10-S.8765. Acta Biomed. 2019. PMID: 31577260 Free PMC article. Review.

9

Genetics of pain: From rare Mendelian disorders to genetic predisposition to pain.

Naureen Z, Lorusso L, Manganotti P, Caruso P, Mazzon G, Cecchin S, Marceddu G, Bertelli M. Naureen Z, et al. Among authors: cecchin s. Acta Biomed. 2020 Nov 9;91(13-S):e2020010. doi: 10.23750/abm.v91i13-S.10682. Acta Biomed. 2020. PMID: 33170156 Free PMC article. Review.

10

Comparison between American and European legislation in the therapeutical and alimentary bacteriophage usage.

Naureen Z, Malacarne D, Anpilogov K, Dautaj A, Camilleri G, Cecchin S, Bressan S, Casadei A, Albion E, Sorrentino E, Beccari T, Dundar M, Bertelli M. Naureen Z, et al. Among authors: cecchin s. Acta Biomed. 2020 Nov 9;91(13-S):e2020023. doi: 10.23750/abm.v91i13-S.10815. Acta Biomed. 2020. PMID: 33170166 Free PMC article. Review.

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