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Pediatric biobanking: a pilot qualitative survey of practices, rules, and researcher opinions in ten European countries.
Salvaterra E, Giorda R, Bassi MT, Borgatti R, Knudsen LE, Martinuzzi A, Nobile M, Pozzoli U, Ramelli GP, Reni GL, Rivolta D, Stazi MA, Strazzer S, Thijs C, Toccaceli V, Trabacca A, Turconi AC, Zanini S, Zucca C, Bresolin N, Lenzi On Behalf Of The Pediatric Biobank Elsi Working Group L. Salvaterra E, et al. Among authors: giorda r. Biopreserv Biobank. 2012 Feb;10(1):29-36. doi: 10.1089/bio.2011.0037. Epub 2011 Dec 13. Biopreserv Biobank. 2012. PMID: 24849751
Exploring the Contribution of Proximal Family Risk Factors on SLC6A4 DNA Methylation in Children with a History of Maltreatment: A Preliminary Study.
Craig F, Mascheroni E, Giorda R, Felline MG, Bacco MG, Castagna A, Tenuta F, Villa M, Costabile A, Trabacca A, Montirosso R. Craig F, et al. Among authors: giorda r. Int J Environ Res Public Health. 2021 Dec 2;18(23):12736. doi: 10.3390/ijerph182312736. Int J Environ Res Public Health. 2021. PMID: 34886461 Free PMC article.
Expanding Phenotype of Poirier-Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients.
Orsini A, Santangelo A, Bravin F, Bonuccelli A, Peroni D, Battini R, Foiadelli T, Bertini V, Valetto A, Iacomino M, Nigro V, Torella AL, Scala M, Capra V, Vari MS, Fetta A, Di Pisa V, Montanari F, Epifanio R, Bonanni P, Giorda R, Operto F, Pastorino G, Sarigecili E, Sardaroglu E, Okuyaz C, Bozdogan S, Musante L, Faletra F, Zanus C, Ferretti A, Vigevano F, Striano P, Cordelli DM. Orsini A, et al. Among authors: giorda r. Genes (Basel). 2022 Jan 30;13(2):276. doi: 10.3390/genes13020276. Genes (Basel). 2022. PMID: 35205321 Free PMC article.
Novel epilepsy phenotype associated to a known SCN8A mutation.
Epifanio R, Zanotta N, Giorda R, Bardoni A, Zucca C. Epifanio R, et al. Among authors: giorda r. Seizure. 2019 Apr;67:15-17. doi: 10.1016/j.seizure.2019.01.017. Epub 2019 Mar 4. Seizure. 2019. PMID: 30851583 Free article. No abstract available.
182 results