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Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review.
Galosi S, Barca E, Carrozzo R, Schirinzi T, Quinzii CM, Lieto M, Vasco G, Zanni G, Di Nottia M, Galatolo D, Filla A, Bertini E, Santorelli FM, Leuzzi V, Haas R, Hirano M, Friedman J. Galosi S, et al. Among authors: vasco g. Parkinsonism Relat Disord. 2019 Nov;68:8-16. doi: 10.1016/j.parkreldis.2019.09.015. Epub 2019 Sep 28. Parkinsonism Relat Disord. 2019. PMID: 31621627 Review.
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency.
Pane M, Messina S, Vasco G, Foley AR, Morandi L, Pegoraro E, Mongini T, D'Amico A, Bianco F, Lombardo ME, Scalise R, Bruno C, Berardinelli A, Pini A, Moroni I, Mora M, Toscano A, Moggio M, Comi G, Santorelli FM, Bertini E, Muntoni F, Mercuri E. Pane M, et al. Among authors: vasco g. Neuromuscul Disord. 2012 Aug;22(8):685-9. doi: 10.1016/j.nmd.2012.05.006. Epub 2012 Jun 22. Neuromuscul Disord. 2012. PMID: 22727687 Free PMC article.
Serum uric acid in Friedreich Ataxia.
Schirinzi T, Vasco G, Zanni G, Petrillo S, Piemonte F, Castelli E, Bertini ES. Schirinzi T, et al. Among authors: vasco g. Clin Biochem. 2018 Apr;54:139-141. doi: 10.1016/j.clinbiochem.2018.01.022. Epub 2018 Feb 2. Clin Biochem. 2018. PMID: 29409831
The impact of next-generation sequencing on the diagnosis of pediatric-onset hereditary spastic paraplegias: new genotype-phenotype correlations for rare HSP-related genes.
Travaglini L, Aiello C, Stregapede F, D'Amico A, Alesi V, Ciolfi A, Bruselles A, Catteruccia M, Pizzi S, Zanni G, Loddo S, Barresi S, Vasco G, Tartaglia M, Bertini E, Nicita F. Travaglini L, et al. Among authors: vasco g. Neurogenetics. 2018 May;19(2):111-121. doi: 10.1007/s10048-018-0545-9. Epub 2018 Apr 24. Neurogenetics. 2018. PMID: 29691679
Longitudinal gait assessment in a stiff person syndrome.
Schirinzi T, Sancesario A, Romano A, Favetta M, Gobbi M, Valeriani M, Bertini ES, Castelli E, Vasco G, Petrarca M, Della Bella G. Schirinzi T, et al. Among authors: vasco g. Int J Rehabil Res. 2018 Dec;41(4):377-379. doi: 10.1097/MRR.0000000000000304. Int J Rehabil Res. 2018. PMID: 30045062
Natural history of a cohort of ABCD1 variant female carriers.
Schirinzi T, Vasco G, Aiello C, Rizzo C, Sancesario A, Romano A, Favetta M, Petrarca M, Paone L, Castelli E, Bertini ES, Cappa M. Schirinzi T, et al. Among authors: vasco g. Eur J Neurol. 2019 Feb;26(2):326-332. doi: 10.1111/ene.13816. Epub 2018 Nov 9. Eur J Neurol. 2019. PMID: 30295399
91 results