Sciacco M - Search Results

1

Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation: a case report.

Ronchi D, Cosi A, Tonduti D, Orcesi S, Bordoni A, Fortunato F, Rizzuti M, Sciacco M, Collotta M, Cagdas S, Capovilla G, Moggio M, Berardinelli A, Veggiotti P, Comi GP. Ronchi D, et al. Among authors: sciacco m. BMC Neurol. 2011 Jul 12;11:85. doi: 10.1186/1471-2377-11-85. BMC Neurol. 2011. PMID: 21749722 Free PMC article.

2

Sural nerve immunoreactivity for nerve growth factor receptor in a case of localized hypertrophic neuropathy.

Sciacco M, Scarpini E, Baron PL, Doronzo R, Moggio M, Passerini D, Scarlato G. Sciacco M, et al. Acta Neuropathol. 1992;83(5):547-53. doi: 10.1007/BF00310035. Acta Neuropathol. 1992. PMID: 1320324

3

Lack of anionic phospholipid calcium binding sites in Duchenne muscular dystrophy.

Moggio M, Fagiolari G, Prelle A, Gallanti A, Sciacco M, Scarlato G. Moggio M, et al. Among authors: sciacco m. Muscle Nerve. 1992 Mar;15(3):325-31. doi: 10.1002/mus.880150311. Muscle Nerve. 1992. PMID: 1557080

4

Appearance and localization of dystrophin in normal human fetal muscle.

Prelle A, Chianese L, Moggio M, Gallanti A, Sciacco M, Checcarelli N, Comi G, Scarpini E, Bonilla E, Scarlato G. Prelle A, et al. Among authors: sciacco m. Int J Dev Neurosci. 1991;9(6):607-12. doi: 10.1016/0736-5748(91)90022-e. Int J Dev Neurosci. 1991. PMID: 1803857

5

Decrease of nerve Na+,K(+)-ATPase activity in the pathogenesis of human diabetic neuropathy.

Scarpini E, Bianchi R, Moggio M, Sciacco M, Fiori MG, Scarlato G. Scarpini E, et al. Among authors: sciacco m. J Neurol Sci. 1993 Dec 15;120(2):159-67. doi: 10.1016/0022-510x(93)90268-4. J Neurol Sci. 1993. PMID: 8138805

6

Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophy.

Moggio M, Prelle A, Fagiolari G, Checcarelli N, Sciacco M, Ciscato P, Scarlato G. Moggio M, et al. Among authors: sciacco m. Muscle Nerve. 1994 May;17(5):485-8. doi: 10.1002/mus.880170503. Muscle Nerve. 1994. PMID: 8159177

7

Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle.

Prelle A, Rigoletto C, Moggio M, Sciacco M, Comi GP, Ciscato P, Fagiolari G, Rapuzzi S, Bignotti V, Scarlato G. Prelle A, et al. Among authors: sciacco m. J Neurol Sci. 1996 Sep 1;140(1-2):132-6. doi: 10.1016/0022-510x(96)00129-3. J Neurol Sci. 1996. PMID: 8866439

8

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.

Comi GP, Bordoni A, Salani S, Franceschina L, Sciacco M, Prelle A, Fortunato F, Zeviani M, Napoli L, Bresolin N, Moggio M, Ausenda CD, Taanman JW, Scarlato G. Comi GP, et al. Among authors: sciacco m. Ann Neurol. 1998 Jan;43(1):110-6. doi: 10.1002/ana.410430119. Ann Neurol. 1998. PMID: 9450776

9

Clinical manifestations of mitochondrial DNA depletion.

Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Among authors: sciacco m. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728

10

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.

Papadimitriou A, Comi GP, Hadjigeorgiou GM, Bordoni A, Sciacco M, Napoli L, Prelle A, Moggio M, Fagiolari G, Bresolin N, Salani S, Anastasopoulos I, Giassakis G, Divari R, Scarlato G. Papadimitriou A, et al. Among authors: sciacco m. Neurology. 1998 Oct;51(4):1086-92. doi: 10.1212/wnl.51.4.1086. Neurology. 1998. PMID: 9781534

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