Mongini T - Search Results

1

The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?

Mancuso M, Orsucci D, Angelini C, Bertini E, Carelli V, Comi GP, Donati A, Minetti C, Moggio M, Mongini T, Servidei S, Tonin P, Toscano A, Uziel G, Bruno C, Ienco EC, Filosto M, Lamperti C, Catteruccia M, Moroni I, Musumeci O, Pegoraro E, Ronchi D, Santorelli FM, Sauchelli D, Scarpelli M, Sciacco M, Valentino ML, Vercelli L, Zeviani M, Siciliano G. Mancuso M, et al. Among authors: mongini t. J Neurol. 2014 Mar;261(3):504-10. doi: 10.1007/s00415-013-7225-3. Epub 2013 Dec 29. J Neurol. 2014. PMID: 24375076

2

Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.

Doriguzzi C, Palmucci L, Mongini T, Bresolin N, Bet L, Comi G, Lala R. Doriguzzi C, et al. Among authors: mongini t. J Neurol Neurosurg Psychiatry. 1989 Jan;52(1):122-5. doi: 10.1136/jnnp.52.1.122. J Neurol Neurosurg Psychiatry. 1989. PMID: 2540284 Free PMC article.

3

A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency.

Silvestri G, Mongini T, Odoardi F, Modoni A, deRosa G, Doriguzzi C, Palmucci L, Tonali P, Servidei S. Silvestri G, et al. Among authors: mongini t. Neurology. 2000 Apr 25;54(8):1693-6. doi: 10.1212/wnl.54.8.1693. Neurology. 2000. PMID: 10762520

4

MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation.

Mongini T, Doriguzzi C, Chiadò-Piat L, Silvestri G, Servidei S, Palmucci L. Mongini T, et al. Clin Neuropathol. 2002 Mar-Apr;21(2):72-6. Clin Neuropathol. 2002. PMID: 12005255

5

Phenotype modulators in myophosphorylase deficiency.

Martinuzzi A, Sartori E, Fanin M, Nascimbeni A, Valente L, Angelini C, Siciliano G, Mongini T, Tonin P, Tomelleri G, Toscano A, Merlini L, Bindoff LA, Bertelli S. Martinuzzi A, et al. Among authors: mongini t. Ann Neurol. 2003 Apr;53(4):497-502. doi: 10.1002/ana.10499. Ann Neurol. 2003. PMID: 12666117

6

Role of gabapentin in spinal muscular atrophy: results of a multicenter, randomized Italian study.

Merlini L, Solari A, Vita G, Bertini E, Minetti C, Mongini T, Mazzoni E, Angelini C, Morandi L. Merlini L, et al. Among authors: mongini t. J Child Neurol. 2003 Aug;18(8):537-41. doi: 10.1177/08830738030180080501. J Child Neurol. 2003. PMID: 13677579 Clinical Trial.

7

Motor function-muscle strength relationship in spinal muscular atrophy.

Merlini L, Bertini E, Minetti C, Mongini T, Morandi L, Angelini C, Vita G. Merlini L, et al. Among authors: mongini t. Muscle Nerve. 2004 Apr;29(4):548-52. doi: 10.1002/mus.20018. Muscle Nerve. 2004. PMID: 15052620

8

SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy.

Tomelleri G, Palmucci L, Tonin P, Mongini T, Marini M, L'erario R, Rizzuto N, Vattemi G. Tomelleri G, et al. Among authors: mongini t. Brain. 2006 Aug;129(Pt 8):2085-92. doi: 10.1093/brain/awl128. Epub 2006 May 19. Brain. 2006. PMID: 16714317

9

McArdle disease: the mutation spectrum of PYGM in a large Italian cohort.

Bruno C, Cassandrini D, Martinuzzi A, Toscano A, Moggio M, Morandi L, Servidei S, Mongini T, Angelini C, Musumeci O, Comi GP, Lamperti C, Filosto M, Zara F, Minetti C. Bruno C, et al. Among authors: mongini t. Hum Mutat. 2006 Jul;27(7):718. doi: 10.1002/humu.9434. Hum Mutat. 2006. PMID: 16786513

10

Facioscapulohumeral muscular dystrophy and occurrence of heart arrhythmia.

Trevisan CP, Pastorello E, Armani M, Angelini C, Nante G, Tomelleri G, Tonin P, Mongini T, Palmucci L, Galluzzi G, Tupler RG, Barchitta A. Trevisan CP, et al. Among authors: mongini t. Eur Neurol. 2006;56(1):1-5. doi: 10.1159/000094248. Epub 2006 Jun 27. Eur Neurol. 2006. PMID: 16804309

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