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Page 1
Mitochondrial disease heterogeneity: a prognostic challenge.
Acta Myol. 2014 Oct;33(2):86-93.
Acta Myol. 2014.
PMID: 25709378
Free PMC article.
Exertional rhabdomyolysis leading to acute kidney injury: when genetic defects are diagnosed in adult life.
Cucchiari D, Colombo I, Amato O, Podestà MA, Reggiani F, Valentino R, Faravelli I, Testolin S, Moggio M, Badalamenti S.
Cucchiari D, et al. Among authors: testolin s.
CEN Case Rep. 2018 May;7(1):62-65. doi: 10.1007/s13730-017-0292-z. Epub 2017 Dec 12.
CEN Case Rep. 2018.
PMID: 29234986
Free PMC article.
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Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophy.
Peverelli L, Testolin S, Villa L, D'Amico A, Petrini S, Favero C, Magri F, Morandi L, Mora M, Mongini T, Bertini E, Sciacco M, Comi GP, Moggio M.
Peverelli L, et al. Among authors: testolin s.
Neurology. 2015 Nov 24;85(21):1886-93. doi: 10.1212/WNL.0000000000002147. Epub 2015 Oct 23.
Neurology. 2015.
PMID: 26497992
Free PMC article.
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Adult polyglucosan body disease: clinical and histological heterogeneity of a large Italian family.
Colombo I, Pagliarani S, Testolin S, Salsano E, Napoli LM, Bordoni A, Salani S, D'Adda E, Morandi L, Farina L, Magri F, Riva M, Prelle A, Sciacco M, Comi GP, Moggio M.
Colombo I, et al. Among authors: testolin s.
Neuromuscul Disord. 2015 May;25(5):423-8. doi: 10.1016/j.nmd.2015.01.015. Epub 2015 Feb 7.
Neuromuscul Disord. 2015.
PMID: 25728520
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Longitudinal follow-up and muscle MRI pattern of two siblings with polyglucosan body myopathy due to glycogenin-1 mutation.
Colombo I, Pagliarani S, Testolin S, Cinnante CM, Fagiolari G, Ciscato P, Bordoni A, Fortunato F, Magri F, Previtali SC, Velardo D, Sciacco M, Comi GP, Moggio M.
Colombo I, et al. Among authors: testolin s.
J Neurol Neurosurg Psychiatry. 2016 Jul;87(7):797-800. doi: 10.1136/jnnp-2015-310553. Epub 2015 Jul 22.
J Neurol Neurosurg Psychiatry. 2016.
PMID: 26203156
No abstract available.
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