Piccolo G - Search Results

1

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families.

Mariotti C, Gellera C, Rimoldi M, Mineri R, Uziel G, Zorzi G, Pareyson D, Piccolo G, Gambi D, Piacentini S, Squitieri F, Capra R, Castellotti B, Di Donato S. Mariotti C, et al. Among authors: piccolo g. Neurol Sci. 2004 Jul;25(3):130-7. doi: 10.1007/s10072-004-0246-z. Neurol Sci. 2004. PMID: 15300460

2

Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).

Zeviani M, Amati P, Bresolin N, Antozzi C, Piccolo G, Toscano A, DiDonato S. Zeviani M, et al. Among authors: piccolo g. Am J Hum Genet. 1991 Feb;48(2):203-11. Am J Hum Genet. 1991. PMID: 1899320 Free PMC article.

3

A multicentre follow-up study of 1152 patients with myasthenia gravis in Italy.

Mantegazza R, Beghi E, Pareyson D, Antozzi C, Peluchetti D, Sghirlanzoni A, Cosi V, Lombardi M, Piccolo G, Tonali P, et al. Mantegazza R, et al. Among authors: piccolo g. J Neurol. 1990 Oct;237(6):339-44. doi: 10.1007/BF00315656. J Neurol. 1990. PMID: 2277266 Clinical Trial.

4

Four novel cases of periaxin-related neuropathy and review of the literature.

Marchesi C, Milani M, Morbin M, Cesani M, Lauria G, Scaioli V, Piccolo G, Fabrizi GM, Cavallaro T, Taroni F, Pareyson D. Marchesi C, et al. Among authors: piccolo g. Neurology. 2010 Nov 16;75(20):1830-8. doi: 10.1212/WNL.0b013e3181fd6314. Neurology. 2010. PMID: 21079185 Review.

5

Combined central and peripheral demyelination: Clinical features, diagnostic findings, and treatment.

Cortese A, Franciotta D, Alfonsi E, Visigalli N, Zardini E, Diamanti L, Prunetti P, Osera C, Gastaldi M, Berzero G, Pichiecchio A, Piccolo G, Lozza A, Piscosquito G, Salsano E, Ceroni M, Moglia A, Bono G, Pareyson D, Marchioni E. Cortese A, et al. Among authors: piccolo g. J Neurol Sci. 2016 Apr 15;363:182-7. doi: 10.1016/j.jns.2016.02.022. Epub 2016 Feb 10. J Neurol Sci. 2016. PMID: 27000248

6

Laryngeal and phrenic nerve involvement in a patient with hereditary neuropathy with liability to pressure palsies (HNPP).

Cortese A, Piccolo G, Lozza A, Schreiber A, Callegari I, Moglia A, Alfonsi E, Pareyson D. Cortese A, et al. Among authors: piccolo g. Neuromuscul Disord. 2016 Jul;26(7):455-8. doi: 10.1016/j.nmd.2016.05.007. Epub 2016 May 12. Neuromuscul Disord. 2016. PMID: 27241821

7

Prognosis of myasthenia gravis: a multicenter follow-up study of 844 patients.

Beghi E, Antozzi C, Batocchi AP, Cornelio F, Cosi V, Evoli A, Lombardi M, Mantegazza R, Monticelli ML, Piccolo G, et al. Beghi E, et al. Among authors: piccolo g. J Neurol Sci. 1991 Dec;106(2):213-20. doi: 10.1016/0022-510x(91)90260-e. J Neurol Sci. 1991. PMID: 1802969 Clinical Trial.

8

Anti-Ma2/Ta antibodies in a woman with primary lateral sclerosis-like phenotype and Sjögren syndrome.

Piccolo G, Tavazzi E, Jarius S, Alfonsi E, Cavagna L, Piccolo L, Zardini E, Voltz R, Franciotta D. Piccolo G, et al. Among authors: piccolo l. Neurol Sci. 2011 Oct;32(5):915-7. doi: 10.1007/s10072-011-0510-y. Epub 2011 Mar 3. Neurol Sci. 2011. PMID: 21369848

9

Acute disseminated encephalomyelitis.

Marchioni E, Tavazzi E, Minoli L, Del Bue S, Ferrante P, Piccolo G, Bastianello S, Ravaglia S. Marchioni E, et al. Among authors: piccolo g. Neurol Sci. 2008 Sep;29 Suppl 2:S286-8. doi: 10.1007/s10072-008-0966-6. Neurol Sci. 2008. PMID: 18690521 Review.

10

Ocular palsy preceding chronic relapsing idiopathic polyneuropathy. Poor response to plasma exchange.

Piccolo G, Martino G. Piccolo G, et al. Ital J Neurol Sci. 1988 Aug;9(4):383-4. doi: 10.1007/BF02334003. Ital J Neurol Sci. 1988. PMID: 3220715

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