Schirinzi T - Search Results

1

Comparison of the Gait Biomechanical Constraints in Three Different Type of Neuromotor Damages.

Minosse S, Favetta M, Romano A, Pisano A, Summa S, Schirinzi T, Vasco G, Castelli E, Petrarca M. Minosse S, et al. Among authors: schirinzi t. Front Hum Neurosci. 2022 Mar 29;16:822205. doi: 10.3389/fnhum.2022.822205. eCollection 2022. Front Hum Neurosci. 2022. PMID: 35422690 Free PMC article.

2

Nrf2-Inducers Counteract Neurodegeneration in Frataxin-Silenced Motor Neurons: Disclosing New Therapeutic Targets for Friedreich's Ataxia.

Petrillo S, Piermarini E, Pastore A, Vasco G, Schirinzi T, Carrozzo R, Bertini E, Piemonte F. Petrillo S, et al. Among authors: schirinzi t. Int J Mol Sci. 2017 Oct 18;18(10):2173. doi: 10.3390/ijms18102173. Int J Mol Sci. 2017. PMID: 29057804 Free PMC article.

3

Serum uric acid in Friedreich Ataxia.

Schirinzi T, Vasco G, Zanni G, Petrillo S, Piemonte F, Castelli E, Bertini ES. Schirinzi T, et al. Clin Biochem. 2018 Apr;54:139-141. doi: 10.1016/j.clinbiochem.2018.01.022. Epub 2018 Feb 2. Clin Biochem. 2018. PMID: 29409831

4

Novel Homozygous KCNJ10 Mutation in a Patient with Non-syndromic Early-Onset Cerebellar Ataxia.

Nicita F, Tasca G, Nardella M, Bellacchio E, Camponeschi I, Vasco G, Schirinzi T, Bertini E, Zanni G. Nicita F, et al. Among authors: schirinzi t. Cerebellum. 2018 Aug;17(4):499-503. doi: 10.1007/s12311-018-0924-7. Cerebellum. 2018. PMID: 29476442

5

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. Int J Rehabil Res. 2018 Dec;41(4):377-379. doi: 10.1097/MRR.0000000000000304. Int J Rehabil Res. 2018. PMID: 30045062

6

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. Eur J Neurol. 2019 Feb;26(2):326-332. doi: 10.1111/ene.13816. Epub 2018 Nov 9. Eur J Neurol. 2019. PMID: 30295399

7

Non-invasive Focal Mechanical Vibrations Delivered by Wearable Devices: An Open-Label Pilot Study in Childhood Ataxia.

Schirinzi T, Romano A, Favetta M, Sancesario A, Burattini R, Summa S, Della Bella G, Castelli E, Bertini E, Petrarca M, Vasco G. Schirinzi T, et al. Front Neurol. 2018 Oct 9;9:849. doi: 10.3389/fneur.2018.00849. eCollection 2018. Front Neurol. 2018. PMID: 30356679 Free PMC article.

8

SLC2A1 mutations are a rare cause of pediatric-onset hereditary spastic paraplegia.

Nicita F, Schirinzi T, Stregapede F, Vasco G, Bertini E, Travaglini L. Nicita F, et al. Among authors: schirinzi t. Eur J Paediatr Neurol. 2019 Mar;23(2):329-332. doi: 10.1016/j.ejpn.2018.12.004. Epub 2018 Dec 18. Eur J Paediatr Neurol. 2019. PMID: 30616884

9

Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review.

Schirinzi T, Garone G, Travaglini L, Vasco G, Galosi S, Rios L, Castiglioni C, Barassi C, Battaglia D, Gambardella ML, Cantonetti L, Graziola F, Marras CE, Castelli E, Bertini E, Capuano A, Leuzzi V. Schirinzi T, et al. Parkinsonism Relat Disord. 2019 Apr;61:19-25. doi: 10.1016/j.parkreldis.2018.11.019. Epub 2018 Nov 16. Parkinsonism Relat Disord. 2019. PMID: 30642806 Review.

10

Response to Jardim and colleagues regarding comments on 'Natural history of a cohort of ABCD1 variant female carriers'.

Schirinzi T, Vasco G, Bertini ES, Cappa M. Schirinzi T, et al. Eur J Neurol. 2019 Aug;26(8):e77. doi: 10.1111/ene.13947. Epub 2019 May 6. Eur J Neurol. 2019. PMID: 31058396 No abstract available.

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