Schirinzi T - Search Results

1

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

2

Assessment of serum uric acid as risk factor for tauopathies.

Schirinzi T, Di Lazzaro G, Colona VL, Imbriani P, Alwardat M, Sancesario GM, Martorana A, Pisani A. Schirinzi T, et al. J Neural Transm (Vienna). 2017 Sep;124(9):1105-1108. doi: 10.1007/s00702-017-1743-6. Epub 2017 Jun 15. J Neural Transm (Vienna). 2017. PMID: 28620833

3

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.

4

ATP1A3-related epileptic encephalopathy responding to ketogenic diet.

Schirinzi T, Graziola F, Cusmai R, Fusco L, Nicita F, Elia M, Travaglini L, Bertini E, Curatolo P, Vigevano F, Capuano A. Schirinzi T, et al. Brain Dev. 2018 May;40(5):433-438. doi: 10.1016/j.braindev.2018.01.002. Epub 2018 Feb 1. Brain Dev. 2018. PMID: 29395663

5

Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 Mutations.

Schirinzi T, Graziola F, Nicita F, Travaglini L, Stregapede F, Valeriani M, Curatolo P, Bertini E, Vigevano F, Capuano A. Schirinzi T, et al. Cerebellum. 2018 Aug;17(4):489-493. doi: 10.1007/s12311-018-0920-y. Cerebellum. 2018. PMID: 29397530

6

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

7

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

8

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

9

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.

10

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

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