Zollino M - Search Results

1

LETM1 couples mitochondrial DNA metabolism and nutrient preference.

Durigon R, Mitchell AL, Jones AW, Manole A, Mennuni M, Hirst EM, Houlden H, Maragni G, Lattante S, Doronzio PN, Dalla Rosa I, Zollino M, Holt IJ, Spinazzola A. Durigon R, et al. Among authors: zollino m. EMBO Mol Med. 2018 Sep;10(9):e8550. doi: 10.15252/emmm.201708550. EMBO Mol Med. 2018. PMID: 30012579 Free PMC article.

2

A novel L67P SOD1 mutation in an Italian ALS patient.

del Grande A, Luigetti M, Conte A, Mancuso I, Lattante S, Marangi G, Stipa G, Zollino M, Sabatelli M. del Grande A, et al. Among authors: zollino m. Amyotroph Lateral Scler. 2011 Mar;12(2):150-2. doi: 10.3109/17482968.2011.551939. Epub 2011 Jan 19. Amyotroph Lateral Scler. 2011. PMID: 21247266

3

SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant.

Luigetti M, Lattante S, Zollino M, Conte A, Marangi G, Del Grande A, Sabatelli M. Luigetti M, et al. Among authors: zollino m. Neurobiol Aging. 2011 Oct;32(10):1924.e15-8. doi: 10.1016/j.neurobiolaging.2011.04.004. Epub 2011 May 28. Neurobiol Aging. 2011. PMID: 21621297

4

Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter.

Iwanowski PS, Panasiuk B, Van Buggenhout G, Murdolo M, Myśliwiec M, Maas NM, Lattante S, Korniszewski L, Posmyk R, Pilch J, Zajączek S, Fryns JP, Zollino M, Midro AT. Iwanowski PS, et al. Among authors: zollino m. Am J Med Genet A. 2011 Aug;155A(8):1833-47. doi: 10.1002/ajmg.a.34005. Epub 2011 Jul 8. Am J Med Genet A. 2011. PMID: 21744486

5

D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation.

Del Grande A, Conte A, Lattante S, Luigetti M, Marangi G, Zollino M, Madia F, Bisogni G, Sabatelli M. Del Grande A, et al. Among authors: zollino m. J Neurol Sci. 2011 Oct 15;309(1-2):31-3. doi: 10.1016/j.jns.2011.07.041. Epub 2011 Aug 11. J Neurol Sci. 2011. PMID: 21839474

6

Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion.

Luigetti M, Quaranta D, Conte A, Piccininni C, Lattante S, Romano A, Silvestri G, Zollino M, Sabatelli M. Luigetti M, et al. Among authors: zollino m. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Jan;14(1):66-9. doi: 10.3109/17482968.2012.692383. Epub 2012 Jun 18. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 22708871

7

A novel compound heterozygous ALS2 mutation in two Italian siblings with juvenile amyotrophic lateral sclerosis.

Luigetti M, Lattante S, Conte A, Romano A, Zollino M, Marangi G, Sabatelli M. Luigetti M, et al. Among authors: zollino m. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Sep;14(5-6):470-2. doi: 10.3109/21678421.2012.756036. Epub 2013 Jan 3. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23282280 No abstract available.

8

Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis.

Sabatelli M, Moncada A, Conte A, Lattante S, Marangi G, Luigetti M, Lucchini M, Mirabella M, Romano A, Del Grande A, Bisogni G, Doronzio PN, Rossini PM, Zollino M. Sabatelli M, et al. Among authors: zollino m. Hum Mol Genet. 2013 Dec 1;22(23):4748-55. doi: 10.1093/hmg/ddt328. Epub 2013 Jul 11. Hum Mol Genet. 2013. PMID: 23847048

9

New ALS-Related Genes Expand the Spectrum Paradigm of Amyotrophic Lateral Sclerosis.

Sabatelli M, Marangi G, Conte A, Tasca G, Zollino M, Lattante S. Sabatelli M, et al. Among authors: zollino m. Brain Pathol. 2016 Mar;26(2):266-75. doi: 10.1111/bpa.12354. Brain Pathol. 2016. PMID: 26780671 Free PMC article. Review.

10

Matrin 3 variants are frequent in Italian ALS patients.

Marangi G, Lattante S, Doronzio PN, Conte A, Tasca G, Monforte M, Patanella AK, Bisogni G, Meleo E, La Spada S, Zollino M, Sabatelli M. Marangi G, et al. Among authors: zollino m. Neurobiol Aging. 2017 Jan;49:218.e1-218.e7. doi: 10.1016/j.neurobiolaging.2016.09.023. Epub 2016 Oct 6. Neurobiol Aging. 2017. PMID: 28029397

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