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Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis.
Magri F, Brusa R, Bello L, Peverelli L, Del Bo R, Govoni A, Cinnante C, Colombo I, Fortunato F, Tironi R, Corti S, Grimoldi N, Sciacco M, Bresolin N, Pegoraro E, Moggio M, Comi GP. Magri F, et al. Among authors: cinnante c. Acta Myol. 2020 Jun 1;39(2):67-82. doi: 10.36185/2532-1900-009. eCollection 2020 Jun. Acta Myol. 2020. PMID: 32904964 Free PMC article.
Transthyretin Asn90 variant: amyloidogenic or non-amyloidogenic role.
Bersano A, Del Bo R, Ballabio E, Cinnante C, Lanfranconi S, Comi GP, Baron P, Bresolin N, Candelise L. Bersano A, et al. Among authors: cinnante c. J Neurol Sci. 2009 Sep 15;284(1-2):113-5. doi: 10.1016/j.jns.2009.04.015. Epub 2009 May 9. J Neurol Sci. 2009. PMID: 19428025
A cortically blind patient with preserved visual imagery.
Zago S, Corti S, Bersano A, Baron P, Conti G, Ballabio E, Lanfranconi S, Cinnante C, Costa A, Cappellari A, Bresolin N. Zago S, et al. Among authors: cinnante c. Cogn Behav Neurol. 2010 Mar;23(1):44-8. doi: 10.1097/WNN.0b013e3181bf2e6e. Cogn Behav Neurol. 2010. PMID: 20299863
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. 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.
Paroxysmal Nocturnal Hemoglobinuria (Pnh): Brain Mri Ischemic Lesions In Neurologically Asymtomatic Patients.
Barcellini W, Scola E, Lanfranconi S, Grottaroli M, Binda F, Fattizzo B, Zaninoni A, Valcamonica G, Cinnante CM, Boschetti C, Buoli M, Altamura CA, Bresolin N, Triulzi F, Zanella A, Cortelezzi A. Barcellini W, et al. Among authors: cinnante cm. Sci Rep. 2018 Jan 11;8(1):476. doi: 10.1038/s41598-017-18936-0. Sci Rep. 2018. PMID: 29323198 Free PMC article.
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature.
Brusa R, Magri F, Papadimitriou D, Govoni A, Del Bo R, Ciscato P, Savarese M, Cinnante C, Walter MC, Abicht A, Bulst S, Corti S, Moggio M, Bresolin N, Nigro V, Comi GP. Brusa R, et al. Among authors: cinnante c. Neuromuscul Disord. 2018 Jun;28(6):532-537. doi: 10.1016/j.nmd.2018.04.006. Epub 2018 Apr 13. Neuromuscul Disord. 2018. PMID: 29759638 Review.
79 results