Paganini L - Search Results

1

Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry.

Bonaparte E, Pesenti C, Fontana L, Falcone R, Paganini L, Marzorati A, Ferrero S, Nosotti M, Mendogni P, Bareggi C, Sirchia SM, Tabano S, Bosari S, Miozzo M. Bonaparte E, et al. Among authors: paganini l. Diagn Pathol. 2018 Jan 12;13(1):4. doi: 10.1186/s13000-017-0683-7. Diagn Pathol. 2018. PMID: 29368620 Free PMC article.

2

Epigenetic effects of chromatin remodeling agents on organotypic cultures.

Sirchia SM, Faversani A, Rovina D, Russo MV, Paganini L, Savi F, Augello C, Rosso L, Del Gobbo A, Tabano S, Bosari S, Miozzo M. Sirchia SM, et al. Among authors: paganini l. Epigenomics. 2016 Mar;8(3):341-58. doi: 10.2217/epi.15.111. Epub 2016 Mar 7. Epigenomics. 2016. PMID: 26949823 Free article.

3

Mass spectrometry-based assay for the molecular diagnosis of glioma: concomitant detection of chromosome 1p/19q codeletion, and IDH1, IDH2, and TERT mutation status.

Pesenti C, Paganini L, Fontana L, Veniani E, Runza L, Ferrero S, Bosari S, Menghi M, Marfia G, Caroli M, Silipigni R, Guerneri S, Tabano S, Miozzo M. Pesenti C, et al. Among authors: paganini l. Oncotarget. 2017 Jul 8;8(34):57134-57148. doi: 10.18632/oncotarget.19103. eCollection 2017 Aug 22. Oncotarget. 2017. PMID: 28915660 Free PMC article.

4

ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men.

Pansa A, Sirchia SM, Melis S, Giacchetta D, Castiglioni M, Colapietro P, Fiori S, Falcone R, Paganini L, Bonaparte E, Colpi G, Miozzo M, Tabano S. Pansa A, et al. Among authors: paganini l. Hum Reprod. 2014 Dec;29(12):2620-7. doi: 10.1093/humrep/deu261. Epub 2014 Oct 14. Hum Reprod. 2014. PMID: 25316452

5

PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosis.

Augello C, Gianelli U, Falcone R, Tabano S, Savi F, Bonaparte E, Ciboddo M, Paganini L, Parafioriti A, Ricca D, Lonati S, Cattaneo D, Fracchiolla NS, Iurlo A, Cortelezzi A, Bosari S, Miozzo M, Sirchia SM. Augello C, et al. Among authors: paganini l. Leuk Res. 2015 Feb;39(2):236-41. doi: 10.1016/j.leukres.2014.11.012. Epub 2014 Dec 2. Leuk Res. 2015. PMID: 25498506 Clinical Trial.

6

Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi.

Paganini L, Carlessi N, Fontana L, Silipigni R, Motta S, Fiori S, Guerneri S, Lalatta F, Cereda A, Sirchia S, Miozzo M, Tabano S. Paganini L, et al. Epigenetics. 2015;10(7):643-9. doi: 10.1080/15592294.2015.1057383. Epigenetics. 2015. PMID: 26061650 Free PMC article.

7

Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.

Bedeschi MF, Calvello M, Paganini L, Pezzani L, Baccarin M, Fontana L, Sirchia SM, Guerneri S, Canazza L, Leva E, Colombo L, Lalatta F, Mosca F, Tabano S, Miozzo M. Bedeschi MF, et al. Among authors: paganini l. BMC Med Genet. 2017 Oct 18;18(1):115. doi: 10.1186/s12881-017-0470-z. BMC Med Genet. 2017. PMID: 29047350 Free PMC article.

8

A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome.

Paganini L, Pesenti C, Milani D, Fontana L, Motta S, Sirchia SM, Scuvera G, Marchisio P, Esposito S, Cinnante CM, Tabano SM, Miozzo MR. Paganini L, et al. Am J Med Genet A. 2018 Jun;176(6):1427-1431. doi: 10.1002/ajmg.a.38704. Epub 2018 Apr 16. Am J Med Genet A. 2018. PMID: 29663667

9

A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins.

Paganini L, Hadi LA, Chetta M, Rovina D, Fontana L, Colapietro P, Bonaparte E, Pezzani L, Marchisio P, Tabano SM, Costanza J, Sirchia SM, Riboni L, Milani D, Miozzo M. Paganini L, et al. Clin Genet. 2019 Mar;95(3):368-374. doi: 10.1111/cge.13485. Epub 2018 Dec 26. Clin Genet. 2019. PMID: 30471091 Free PMC article.

10

STAR syndrome plus: The first description of a female patient with the lethal form.

Bedeschi MF, Giangiobbe S, Paganini L, Tabano S, Silipigni R, Colombo L, Crippa BL, Lalatta F, Guerneri S, Miozzo M. Bedeschi MF, et al. Among authors: paganini l. Am J Med Genet A. 2017 Dec;173(12):3226-3230. doi: 10.1002/ajmg.a.38484. Epub 2017 Oct 31. Am J Med Genet A. 2017. PMID: 29088509

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