Marchina E - Search Results

1

VKORC1 and CYP2C9 polymorphisms related to adverse events in case-control cohort of anticoagulated patients.

Misasi S, Martini G, Paoletti O, Calza S, Scovoli G, Marengoni A, Testa S, Caimi L, Marchina E. Misasi S, et al. Among authors: marchina e. Medicine (Baltimore). 2016 Dec;95(52):e5451. doi: 10.1097/MD.0000000000005451. Medicine (Baltimore). 2016. PMID: 28033245 Free PMC article.

2

BRCA1 and BRCA2 genetic test in high risk patients and families: counselling and management.

Marchina E, Fontana MG, Speziani M, Salvi A, Ricca G, Di Lorenzo D, Gervasi M, Caimi L, Barlati S. Marchina E, et al. Oncol Rep. 2010 Dec;24(6):1661-7. doi: 10.3892/or_00001031. Oncol Rep. 2010. PMID: 21042765

3

Gene expression profile in fibroblasts of Huntington's disease patients and controls.

Marchina E, Misasi S, Bozzato A, Ferraboli S, Agosti C, Rozzini L, Borsani G, Barlati S, Padovani A. Marchina E, et al. J Neurol Sci. 2014 Feb 15;337(1-2):42-6. doi: 10.1016/j.jns.2013.11.014. Epub 2013 Nov 21. J Neurol Sci. 2014. PMID: 24296361

4

Rapid Point-Of-Care Serology and Clinical History Assessment Increase Protection Provided by RT-PCR Screening: A Pilot Study Involving Three Nursing Homes in Brescia, a Hotspot of Lombardy.

Savio A, Calza S, Guerrini G, Romano V, Marchina E. Savio A, et al. Among authors: marchina e. Front Public Health. 2021 Jun 24;9:649524. doi: 10.3389/fpubh.2021.649524. eCollection 2021. Front Public Health. 2021. PMID: 34249831 Free PMC article.

5

Mesenchymal cells from human amniotic fluid survive and migrate after transplantation into adult rat brain.

Cipriani S, Bonini D, Marchina E, Balgkouranidou I, Caimi L, Grassi Zucconi G, Barlati S. Cipriani S, et al. Among authors: marchina e. Cell Biol Int. 2007 Aug;31(8):845-50. doi: 10.1016/j.cellbi.2007.01.037. Epub 2007 Feb 9. Cell Biol Int. 2007. PMID: 17379545

6

SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement.

Magri C, Marchina E, Bertini V, Traversa M, Savio G, Pilotta A, Piovani G. Magri C, et al. Among authors: marchina e. BMC Med Genet. 2015 Jul 7;16:47. doi: 10.1186/s12881-015-0193-y. BMC Med Genet. 2015. PMID: 26149167 Free PMC article.

7

Choreo-athetosis in LRRK2 R1441C mutation: expanding the clinical phenotype.

Borroni B, Cotelli MS, Marchina E, Filosto M, Premi E, Padovani A. Borroni B, et al. Among authors: marchina e. Clin Neurol Neurosurg. 2013 Oct;115(10):2217-8. doi: 10.1016/j.clineuro.2013.06.020. Epub 2013 Jul 27. Clin Neurol Neurosurg. 2013. PMID: 23895867 No abstract available.

8

Phenotypic heterogeneity of Niemann-Pick disease type C in monozygotic twins.

Benussi A, Alberici A, Premi E, Bertasi V, Cotelli MS, Turla M, Dardis A, Zampieri S, Marchina E, Paghera B, Gallivanone F, Castiglioni I, Padovani A, Borroni B. Benussi A, et al. Among authors: marchina e. J Neurol. 2015 Mar;262(3):642-7. doi: 10.1007/s00415-014-7619-x. Epub 2014 Dec 24. J Neurol. 2015. PMID: 25536905

9

Very late-onset friedreich ataxia with laryngeal dystonia.

Rota S, Marchina E, Todeschini A, Nanetti L, Rinaldi F, Vanotti A, Mariotti C, Padovani A, Filosto M. Rota S, et al. Among authors: marchina e. Case Rep Neurol. 2014 Dec 12;6(3):287-90. doi: 10.1159/000370062. eCollection 2014 Sep-Dec. Case Rep Neurol. 2014. PMID: 25685137 Free PMC article.

10

A novel mitochondrial tRNA(Ala) gene variant causes chronic progressive external ophthalmoplegia in a patient with Huntington disease.

Filosto M, Lanzi G, Nesti C, Vielmi V, Marchina E, Galvagni A, Giliani S, Santorelli FM, Padovani A. Filosto M, et al. Among authors: marchina e. Mol Genet Metab Rep. 2016 Feb 27;6:70-3. doi: 10.1016/j.ymgmr.2016.02.001. eCollection 2016 Mar. Mol Genet Metab Rep. 2016. PMID: 27014581 Free PMC article.

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