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Page 1
First Results of an External Quality Assessment (EQA) Scheme for Molecular, Serological and Antigenic Diagnostic Test for SARS-CoV-2 Detection in Lombardy Region (Northern Italy), 2020-2022.
Diagnostics (Basel). 2022 Jun 16;12(6):1483. doi: 10.3390/diagnostics12061483.
Diagnostics (Basel). 2022.
PMID: 35741293
Free PMC article.
Glutamine Synthetase 1 Increases Autophagy Lysosomal Degradation of Mutant Huntingtin Aggregates in Neurons, Ameliorating Motility in a Drosophila Model for Huntington's Disease.
Vernizzi L, Paiardi C, Licata G, Vitali T, Santarelli S, Raneli M, Manelli V, Rizzetto M, Gioria M, Pasini ME, Grifoni D, Vanoni MA, Gellera C, Taroni F, Bellosta P.
Vernizzi L, et al. Among authors: rizzetto m.
Cells. 2020 Jan 13;9(1):196. doi: 10.3390/cells9010196.
Cells. 2020.
PMID: 31941072
Free PMC article.
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Mesenchymal stromal cells uptake and release paclitaxel without reducing its anticancer activity.
Mariotti M, Colognato R, Rimoldi M, Rizzetto M, Sisto F, Cocce V, Bonomi A, Parati E, Alessandri G, Bagnati R, Pessina A.
Mariotti M, et al. Among authors: rizzetto m.
Anticancer Agents Med Chem. 2015;15(3):400-5. doi: 10.2174/1871520614666140618113441.
Anticancer Agents Med Chem. 2015.
PMID: 24942547
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Human CD14+ cells loaded with Paclitaxel inhibit in vitro cell proliferation of glioblastoma.
Bonomi A, Lisini D, Navone SE, Frigerio S, Dossena M, Ciusani E, Rampini P, Marfia G, Coccè V, Cavicchini L, Sisto F, Parati E, Mantegazza R, Rimoldi M, Rizzetto M, Alessandri G, Pessina A.
Bonomi A, et al. Among authors: rizzetto m.
Cytotherapy. 2015 Mar;17(3):310-9. doi: 10.1016/j.jcyt.2014.09.009. Epub 2014 Oct 28.
Cytotherapy. 2015.
PMID: 25457277
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Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency with unknown genetic defect.
Cotelli MS, Vielmi V, Rimoldi M, Rizzetto M, Castellotti B, Bertasi V, Todeschini A, Gregorelli V, Baronchelli C, Gellera C, Padovani A, Filosto M.
Cotelli MS, et al. Among authors: rizzetto m.
Neurol Sci. 2012 Dec;33(6):1383-7. doi: 10.1007/s10072-011-0900-1. Epub 2011 Dec 22.
Neurol Sci. 2012.
PMID: 22190129
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PEX7 Mutations Cause Congenital Cataract Retinopathy and Late-Onset Ataxia and Cognitive Impairment: Report of Two Siblings and Review of the Literature.
Nanetti L, Pensato V, Leoni V, Rizzetto M, Caccia C, Taroni F, Mariotti C, Gellera C.
Nanetti L, et al. Among authors: rizzetto m.
J Clin Neurol. 2015 Apr;11(2):197-9. doi: 10.3988/jcn.2015.11.2.197.
J Clin Neurol. 2015.
PMID: 25851898
Free PMC article.
No abstract available.
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Hyperargininemia: 7-month follow-up under sodium benzoate therapy in an Italian child presenting progressive spastic paraparesis, cognitive decline, and novel mutation in ARG1 gene.
Baranello G, Alfei E, Martinelli D, Rizzetto M, Cazzaniga F, Dionisi-Vici C, Gellera C, Castellotti B.
Baranello G, et al. Among authors: rizzetto m.
Pediatr Neurol. 2014 Sep;51(3):430-3. doi: 10.1016/j.pediatrneurol.2014.05.029. Epub 2014 Jun 4.
Pediatr Neurol. 2014.
PMID: 24997092
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