Ferrari M - Search Results

1

Association of LOXIN, a new functional splicing isoform of the OLR1 gene, with severity and prognostic localization of critical coronary artery stenoses.

Cappelletti A, Zanussi M, Mazzavillani M, Magni V, Calori G, Godino C, Ferrari M, Margonato A. Cappelletti A, et al. Among authors: ferrari m. J Cardiovasc Med (Hagerstown). 2014 May;15(5):391-6. doi: 10.2459/JCM.0b013e3283624251. J Cardiovasc Med (Hagerstown). 2014. PMID: 24743687

2

Loss of mismatched HLA in leukemia after stem-cell transplantation.

Vago L, Perna SK, Zanussi M, Mazzi B, Barlassina C, Stanghellini MT, Perrelli NF, Cosentino C, Torri F, Angius A, Forno B, Casucci M, Bernardi M, Peccatori J, Corti C, Bondanza A, Ferrari M, Rossini S, Roncarolo MG, Bordignon C, Bonini C, Ciceri F, Fleischhauer K. Vago L, et al. Among authors: ferrari m. N Engl J Med. 2009 Jul 30;361(5):478-88. doi: 10.1056/NEJMoa0811036. N Engl J Med. 2009. PMID: 19641204 Free article.

3

Evaluation of the Universal Master Mix (STAT-NAT DNA-Mix) for reliable molecular testing.

Castiglioni E, Gramegna M, Moiana A, Zanussi M, Ferrari M. Castiglioni E, et al. Among authors: ferrari m. Clin Chem Lab Med. 2013 Jun;51(6):e133-6. doi: 10.1515/cclm-2012-0514. Clin Chem Lab Med. 2013. PMID: 23241611 No abstract available.

4

Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination.

Percesepe A, Ferrari M, Coviello D, Zanussi M, Castagni M, Neri I, Travi M, Forabosco A, Tedeschi S. Percesepe A, et al. Among authors: ferrari m. Prenat Diagn. 2005 Nov;25(11):1011-4. doi: 10.1002/pd.1238. Prenat Diagn. 2005. PMID: 16231306

5

Genetic predisposing factors to bronchopulmonary dysplasia: preliminary data from a multicentre study.

Somaschini M, Castiglioni E, Volonteri C, Cursi M, Ferrari M, Carrera P. Somaschini M, et al. Among authors: ferrari m. J Matern Fetal Neonatal Med. 2012 Oct;25 Suppl 4:127-30. doi: 10.3109/14767058.2012.714995. J Matern Fetal Neonatal Med. 2012. PMID: 22958043

6

Single-nucleotide polymorphism and mutation identification by the nanogen microelectronic chip technology.

Ferrari M, Cremonesi L, Bonini P, Foglieni B, Stenirri S. Ferrari M, et al. Methods Mol Med. 2005;114:93-106. doi: 10.1385/1-59259-923-0:93. Methods Mol Med. 2005. PMID: 16156099

7

A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia.

Foglieni B, Galbiati S, Ferrari M, Cremonesi L. Foglieni B, et al. Among authors: ferrari m. Methods Mol Biol. 2008;444:169-82. doi: 10.1007/978-1-59745-066-9_13. Methods Mol Biol. 2008. PMID: 18425480

8

A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia.

Rossi D, Gigli L, Gamberucci A, Bordoni R, Pietrelli A, Lorenzini S, Pierantozzi E, Peretto G, De Bellis G, Della Bella P, Ferrari M, Sorrentino V, Benedetti S, Sala S, Di Resta C. Rossi D, et al. Among authors: ferrari m. Heart Rhythm. 2020 Feb;17(2):296-304. doi: 10.1016/j.hrthm.2019.08.018. Epub 2019 Aug 19. Heart Rhythm. 2020. PMID: 31437535

9

Molecular diagnostics by microelectronic microchips.

Ferrari M, Stenirri S, Bonini P, Cremonesi L. Ferrari M, et al. Clin Chem Lab Med. 2003 Apr;41(4):462-7. doi: 10.1515/CCLM.2003.069. Clin Chem Lab Med. 2003. PMID: 12747587 Review.

10

Analysis of ferritin genes in Parkinson disease.

Foglieni B, Ferrari F, Goldwurm S, Santambrogio P, Castiglioni E, Sessa M, Volontè MA, Lalli S, Galli C, Wang XS, Connor J, Sironi F, Canesi M, Biasiotto G, Pezzoli G, Levi S, Ferrari M, Arosio P, Cremonesi L. Foglieni B, et al. Among authors: ferrari m, ferrari f. Clin Chem Lab Med. 2007;45(11):1450-6. doi: 10.1515/CCLM.2007.307. Clin Chem Lab Med. 2007. PMID: 17970701

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