Moroni I - Search Results

1

SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.

Nanetti L, Cavalieri S, Pensato V, Erbetta A, Pareyson D, Panzeri M, Zorzi G, Antozzi C, Moroni I, Gellera C, Brusco A, Mariotti C. Nanetti L, et al. Among authors: moroni i. Orphanet J Rare Dis. 2013 Aug 14;8:123. doi: 10.1186/1750-1172-8-123. Orphanet J Rare Dis. 2013. PMID: 23941260 Free PMC article.

2

Childhood-onset multifocal motor neuropathy with conduction blocks.

Moroni I, Bugiani M, Ciano C, Bono R, Pareyson D. Moroni I, et al. Neurology. 2006 Mar 28;66(6):922-4. doi: 10.1212/01.wnl.0000203346.25068.3f. Neurology. 2006. PMID: 16567714

3

Classification of childhood white matter disorders using proton MR spectroscopic imaging.

Bizzi A, Castelli G, Bugiani M, Barker PB, Herskovits EH, Danesi U, Erbetta A, Moroni I, Farina L, Uziel G. Bizzi A, et al. Among authors: moroni i. AJNR Am J Neuroradiol. 2008 Aug;29(7):1270-5. doi: 10.3174/ajnr.A1106. Epub 2008 May 15. AJNR Am J Neuroradiol. 2008. PMID: 18483189 Free PMC article.

4

Novel mutations in the GDAP1 gene in patients affected with early-onset axonal Charcot-Marie-Tooth type 4A.

Moroni I, Morbin M, Milani M, Ciano C, Bugiani M, Pagliano E, Cavallaro T, Pareyson D, Taroni F. Moroni I, et al. Neuromuscul Disord. 2009 Jul;19(7):476-80. doi: 10.1016/j.nmd.2009.04.014. Epub 2009 Jun 4. Neuromuscul Disord. 2009. PMID: 19500985

5

Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.

Castellotti B, Mariotti C, Rimoldi M, Fancellu R, Plumari M, Caimi S, Uziel G, Nardocci N, Moroni I, Zorzi G, Pareyson D, Di Bella D, Di Donato S, Taroni F, Gellera C. Castellotti B, et al. Among authors: moroni i. Neurogenetics. 2011 Aug;12(3):193-201. doi: 10.1007/s10048-011-0281-x. Epub 2011 Apr 5. Neurogenetics. 2011. PMID: 21465257

6

Outcome measures for Charcot-Marie-Tooth disease: clinical and neurofunctional assessment in children.

Pagliano E, Moroni I, Baranello G, Magro A, Marchi A, Bulgheroni S, Ferrarin M, Pareyson D. Pagliano E, et al. Among authors: moroni i. J Peripher Nerv Syst. 2011 Sep;16(3):237-242. doi: 10.1111/j.1529-8027.2011.00357.x. J Peripher Nerv Syst. 2011. PMID: 22003938 Free PMC article.

7

Cortical myoclonus in childhood and juvenile onset Huntington's disease.

Rossi Sebastiano D, Soliveri P, Panzica F, Moroni I, Gellera C, Gilioli I, Nardocci N, Ciano C, Albanese A, Franceschetti S, Canafoglia L. Rossi Sebastiano D, et al. Among authors: moroni i. Parkinsonism Relat Disord. 2012 Jul;18(6):794-7. doi: 10.1016/j.parkreldis.2012.03.011. Epub 2012 Apr 10. Parkinsonism Relat Disord. 2012. PMID: 22494662

8

Changes of gait pattern in children with Charcot-Marie-Tooth disease type 1A: a 18 months follow-up study.

Ferrarin M, Lencioni T, Rabuffetti M, Moroni I, Pagliano E, Pareyson D. Ferrarin M, et al. Among authors: moroni i. J Neuroeng Rehabil. 2013 Jul 2;10:65. doi: 10.1186/1743-0003-10-65. J Neuroeng Rehabil. 2013. PMID: 23819439 Free PMC article.

9

Peripheral neuropathy in mitochondrial disorders.

Pareyson D, Piscosquito G, Moroni I, Salsano E, Zeviani M. Pareyson D, et al. Among authors: moroni i. Lancet Neurol. 2013 Oct;12(10):1011-24. doi: 10.1016/S1474-4422(13)70158-3. Lancet Neurol. 2013. PMID: 24050734 Review.

10

Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48.

Pensato V, Castellotti B, Gellera C, Pareyson D, Ciano C, Nanetti L, Salsano E, Piscosquito G, Sarto E, Eoli M, Moroni I, Soliveri P, Lamperti E, Chiapparini L, Di Bella D, Taroni F, Mariotti C. Pensato V, et al. Among authors: moroni i. Brain. 2014 Jul;137(Pt 7):1907-20. doi: 10.1093/brain/awu121. Epub 2014 May 15. Brain. 2014. PMID: 24833714

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