Zollino M - Search Results

1

HFE p.H63D polymorphism does not influence ALS phenotype and survival.

Chiò A, Mora G, Sabatelli M, Caponnetto C, Lunetta C, Traynor BJ, Johnson JO, Nalls MA, Calvo A, Moglia C, Borghero G, Monsurrò MR, La Bella V, Volanti P, Simone I, Salvi F, Logullo FO, Nilo R, Giannini F, Mandrioli J, Tanel R, Murru MR, Mandich P, Zollino M, Conforti FL, Penco S; ITALSGEN consortium; SARDINIALS consortium; Brunetti M, Barberis M, Restagno G. Chiò A, et al. Among authors: zollino m. Neurobiol Aging. 2015 Oct;36(10):2906.e7-11. doi: 10.1016/j.neurobiolaging.2015.06.016. Epub 2015 Jun 18. Neurobiol Aging. 2015. PMID: 26174855 Free PMC article.

2

Natural history of young-adult amyotrophic lateral sclerosis.

Sabatelli M, Madia F, Conte A, Luigetti M, Zollino M, Mancuso I, Lo Monaco M, Lippi G, Tonali P. Sabatelli M, et al. Among authors: zollino m. Neurology. 2008 Sep 16;71(12):876-81. doi: 10.1212/01.wnl.0000312378.94737.45. Epub 2008 Jul 2. Neurology. 2008. PMID: 18596241

3

Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis.

Luigetti M, Conte A, Madia F, Marangi G, Zollino M, Mancuso I, Dileone M, Del Grande A, Di Lazzaro V, Tonali PA, Sabatelli M. Luigetti M, et al. Among authors: zollino m. Neurol Sci. 2009 Dec;30(6):517-20. doi: 10.1007/s10072-009-0125-8. Epub 2009 Aug 15. Neurol Sci. 2009. PMID: 19685200

4

SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis.

Luigetti M, Madia F, Conte A, Marangi G, Zollino M, Del Grande A, Dileone M, Tonali PA, Sabatelli M. Luigetti M, et al. Among authors: zollino m. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):479-82. doi: 10.3109/17482960802302261. Amyotroph Lateral Scler. 2009. PMID: 19922144

5

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

6

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

7

Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS.

Sabatelli M, Zollino M, Luigetti M, Grande AD, Lattante S, Marangi G, Monaco ML, Madia F, Meleo E, Bisogni G, Conte A. Sabatelli M, et al. Among authors: zollino m. Amyotroph Lateral Scler. 2011 Jul;12(4):278-82. doi: 10.3109/17482968.2011.580849. Amyotroph Lateral Scler. 2011. PMID: 21702734

8

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

9

P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis.

Conte A, Lattante S, Zollino M, Marangi G, Luigetti M, Del Grande A, Servidei S, Trombetta F, Sabatelli M. Conte A, et al. Among authors: zollino m. Neuromuscul Disord. 2012 Jan;22(1):73-5. doi: 10.1016/j.nmd.2011.08.003. Epub 2011 Sep 9. Neuromuscul Disord. 2012. PMID: 21907581

10

Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients.

Lattante S, Marangi G, Luigetti M, Conte A, Mandrioli J, Del Grande A, Zollino M, Sabatelli M. Lattante S, et al. Among authors: zollino m. Amyotroph Lateral Scler. 2012 Feb;13(2):241-2. doi: 10.3109/17482968.2011.633269. Amyotroph Lateral Scler. 2012. PMID: 22292847 No abstract available.

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