Magnani C - Search Results

1

Molecular Polymorphisms of Vascular Endothelial Growth Factor Gene and Bronchopulmonary Dysplasia in Very Low Birth Weight Infants.

Filonzi L, Perrone S, Tataranno ML, Magnani C, Dadomo H, Bottoni A, Vaghi M, Nonnis Marzano F. Filonzi L, et al. Among authors: magnani c. Dis Markers. 2022 Sep 1;2022:2793846. doi: 10.1155/2022/2793846. eCollection 2022. Dis Markers. 2022. PMID: 36092960 Free PMC article.

2

Detoxification genes polymorphisms in SIDS exposed to tobacco smoke.

Filonzi L, Magnani C, Lavezzi AM, Vaghi M, Nosetti L, Nonnis Marzano F. Filonzi L, et al. Among authors: magnani c. Gene. 2018 Mar 30;648:1-4. doi: 10.1016/j.gene.2018.01.034. Epub 2018 Jan 9. Gene. 2018. PMID: 29329929

3

Evidence that polymorphic deletion of the glutathione S-transferase gene, GSTM1, is associated with esophageal atresia.

Filonzi L, Magnani C, de' Angelis GL, Dallaglio S, Nonnis Marzano F. Filonzi L, et al. Among authors: magnani c. Birth Defects Res A Clin Mol Teratol. 2010 Sep;88(9):743-7. doi: 10.1002/bdra.20715. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 20740495

4

Serotonin transporter role in identifying similarities between SIDS and idiopathic ALTE.

Filonzi L, Magnani C, Nosetti L, Nespoli L, Borghi C, Vaghi M, Nonnis Marzano F. Filonzi L, et al. Among authors: magnani c. Pediatrics. 2012 Jul;130(1):e138-44. doi: 10.1542/peds.2011-3331. Epub 2012 Jun 18. Pediatrics. 2012. PMID: 22711722

5

Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome.

Nonnis Marzano F, Maldini M, Filonzi L, Lavezzi AM, Parmigiani S, Magnani C, Bevilacqua G, Matturri L. Nonnis Marzano F, et al. Among authors: magnani c. Genomics. 2008 Jun;91(6):485-91. doi: 10.1016/j.ygeno.2008.01.010. Epub 2008 Apr 2. Genomics. 2008. PMID: 18387780 Free article.

6

ALTE and smoking exposure: which role of detoxification genes polymorphisms?

Filonzi L, Nosetti L, Magnani C, Vaghi M, Nganso Fenjiep AF, Marzano FN. Filonzi L, et al. Among authors: magnani c. Clin Genet. 2016 Oct;90(4):383-4. doi: 10.1111/cge.12788. Epub 2016 May 24. Clin Genet. 2016. PMID: 27220633 No abstract available.

7

Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis.

Filonzi L, Magnani C, Lavezzi AM, Rindi G, Parmigiani S, Bevilacqua G, Matturri L, Marzano FN. Filonzi L, et al. Among authors: magnani c. Neurogenetics. 2009 Feb;10(1):65-72. doi: 10.1007/s10048-008-0149-x. Epub 2008 Sep 23. Neurogenetics. 2009. PMID: 18810510

8

Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome.

Filonzi L, Magnani C, Marzano FN. Filonzi L, et al. Among authors: magnani c. Neurogenetics. 2011 Feb;12(1):91-2. doi: 10.1007/s10048-010-0257-2. Epub 2010 Sep 7. Neurogenetics. 2011. PMID: 20820831 No abstract available.

9

Predictors of full enteral feeding achievement in very low birth weight infants.

Corvaglia L, Fantini MP, Aceti A, Gibertoni D, Rucci P, Baronciani D, Faldella G; "Emilia Romagna Perinatal Network". Corvaglia L, et al. PLoS One. 2014 Mar 19;9(3):e92235. doi: 10.1371/journal.pone.0092235. eCollection 2014. PLoS One. 2014. PMID: 24647523 Free PMC article.

10

Determinants of neonatal hypoglycemia after antenatal administration of corticosteroids (ACS) for lung maturation: Data from two referral centers and review of the literature.

di Pasquo E, Saccone G, Angeli L, Dall'Asta A, Borghi E, Fieni S, Berghella V, Magnani C, Frusca T, Ghi T. di Pasquo E, et al. Among authors: magnani c. Early Hum Dev. 2020 Apr;143:104984. doi: 10.1016/j.earlhumdev.2020.104984. Epub 2020 Feb 21. Early Hum Dev. 2020. PMID: 32092675

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