Acquaviva M - Search Results

1

Identification of multiple hypoxia signatures in neuroblastoma cell lines by l1-l2 regularization and data reduction.

Fardin P, Cornero A, Barla A, Mosci S, Acquaviva M, Rosasco L, Gambini C, Verri A, Varesio L. Fardin P, et al. Among authors: acquaviva m. J Biomed Biotechnol. 2010;2010:878709. doi: 10.1155/2010/878709. Epub 2010 Jun 28. J Biomed Biotechnol. 2010. PMID: 20652058 Free PMC article.

2

Design of a multi-signature ensemble classifier predicting neuroblastoma patients' outcome.

Cornero A, Acquaviva M, Fardin P, Versteeg R, Schramm A, Eva A, Bosco MC, Blengio F, Barzaghi S, Varesio L. Cornero A, et al. Among authors: acquaviva m. BMC Bioinformatics. 2012 Mar 28;13 Suppl 4(Suppl 4):S13. doi: 10.1186/1471-2105-13-S4-S13. BMC Bioinformatics. 2012. PMID: 22536959 Free PMC article.

3

Transcriptome analysis defines myocardium gene signatures in children with ToF and ASD and reveals disease-specific molecular reprogramming in response to surgery with cardiopulmonary bypass.

Raggi F, Cangelosi D, Becherini P, Blengio F, Morini M, Acquaviva M, Belli ML, Panizzon G, Cervo G, Varesio L, Eva A, Bosco MC. Raggi F, et al. Among authors: acquaviva m. J Transl Med. 2020 Jan 10;18(1):21. doi: 10.1186/s12967-020-02210-5. J Transl Med. 2020. PMID: 31924244 Free PMC article.

4

Inferring Multiple Sclerosis Stages from the Blood Transcriptome via Machine Learning.

Acquaviva M, Menon R, Di Dario M, Dalla Costa G, Romeo M, Sangalli F, Colombo B, Moiola L, Martinelli V, Comi G, Farina C. Acquaviva M, et al. Cell Rep Med. 2020 Jul 21;1(4):100053. doi: 10.1016/j.xcrm.2020.100053. eCollection 2020 Jul 21. Cell Rep Med. 2020. PMID: 33205062 Free PMC article.

5

Assessment of copy number variations in 120 patients with Poland syndrome.

Vaccari CM, Tassano E, Torre M, Gimelli S, Divizia MT, Romanini MV, Bossi S, Musante I, Valle M, Senes F, Catena N, Bedeschi MF, Baban A, Calevo MG, Acquaviva M, Lerone M, Ravazzolo R, Puliti A. Vaccari CM, et al. Among authors: acquaviva m. BMC Med Genet. 2016 Nov 25;17(1):89. doi: 10.1186/s12881-016-0351-x. BMC Med Genet. 2016. PMID: 27884122 Free PMC article.

6

Loss of Circulating CD8+ CD161^high T Cells in Primary Progressive Multiple Sclerosis.

Acquaviva M, Bassani C, Sarno N, Dalla Costa G, Romeo M, Sangalli F, Colombo B, Moiola L, Martinelli V, Comi G, Farina C. Acquaviva M, et al. Front Immunol. 2019 Aug 14;10:1922. doi: 10.3389/fimmu.2019.01922. eCollection 2019. Front Immunol. 2019. PMID: 31474991 Free PMC article.

7

Convergence between Microglia and Peripheral Macrophages Phenotype during Development and Neuroinflammation.

Grassivaro F, Menon R, Acquaviva M, Ottoboni L, Ruffini F, Bergamaschi A, Muzio L, Farina C, Martino G. Grassivaro F, et al. Among authors: acquaviva m. J Neurosci. 2020 Jan 22;40(4):784-795. doi: 10.1523/JNEUROSCI.1523-19.2019. Epub 2019 Dec 9. J Neurosci. 2020. PMID: 31818979 Free PMC article.

8

WES in a family trio suggests involvement of TECPR2 in a complex form of progressive motor neuron disease.

Covone AE, Fiorillo C, Acquaviva M, Trucco F, Morana G, Ravazzolo R, Minetti C. Covone AE, et al. Among authors: acquaviva m. Clin Genet. 2016 Aug;90(2):182-5. doi: 10.1111/cge.12730. Epub 2016 Feb 10. Clin Genet. 2016. PMID: 27406698

9

Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease.

Mandich P, Grandis M, Geroldi A, Acquaviva M, Varese A, Gulli R, Ciotti P, Bellone E. Mandich P, et al. Among authors: acquaviva m. J Hum Genet. 2008;53(6):529-533. doi: 10.1007/s10038-008-0280-4. Epub 2008 Apr 1. J Hum Genet. 2008. PMID: 18379723

10

Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies.

Mandich P, Fossa P, Capponi S, Geroldi A, Acquaviva M, Gulli R, Ciotti P, Manganelli F, Grandis M, Bellone E. Mandich P, et al. Among authors: acquaviva m. Eur J Hum Genet. 2009 Sep;17(9):1129-34. doi: 10.1038/ejhg.2009.37. Epub 2009 Mar 18. Eur J Hum Genet. 2009. PMID: 19293842 Free PMC article.

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