Triulzi F - Search Results

1

MCT8 deficiency: extrapyramidal symptoms and delayed myelination as prominent features.

Tonduti D, Vanderver A, Berardinelli A, Schmidt JL, Collins CD, Novara F, Genni AD, Mita A, Triulzi F, Brunstrom-Hernandez JE, Zuffardi O, Balottin U, Orcesi S. Tonduti D, et al. Among authors: triulzi f. J Child Neurol. 2013 Jun;28(6):795-800. doi: 10.1177/0883073812450944. Epub 2012 Jul 17. J Child Neurol. 2013. PMID: 22805248 Free PMC article.

2

Bilateral perisylvian polymicrogyria in three generations.

Borgatti R, Triulzi F, Zucca C, Piccinelli P, Balottin U, Carrozzo R, Guerrini R. Borgatti R, et al. Among authors: triulzi f. Neurology. 1999 Jun 10;52(9):1910-3. doi: 10.1212/wnl.52.9.1910. Neurology. 1999. PMID: 10371547

3

Congenital Cytomegalovirus Infection With Isolated "Minor" Lesions at Fetal Magnetic Resonance Imaging: Long-Term Neurological Outcome.

Doneda C, Scelsa B, Introvini P, Zavattoni M, Orcesi S, Lombardi G, Pugni L, Fumagalli M, Rustico M, Vola E, Arrigoni F, Fabbri E, Tortora M, Izzo G, Genovese M, Parazzini C, Tassis B, Ronchi A, Pietrasanta C, Triulzi F, Righini A. Doneda C, et al. Among authors: triulzi f. Pediatr Neurol. 2024 Jun;155:104-113. doi: 10.1016/j.pediatrneurol.2024.03.001. Epub 2024 Mar 7. Pediatr Neurol. 2024. PMID: 38631078

4

Correlation between multimodal evoked potentials and magnetic resonance imaging in multiple sclerosis.

Comi G, Martinelli V, Medaglini S, Locatelli T, Filippi M, Canal N, Triulzi F, Del Maschio A. Comi G, et al. Among authors: triulzi f. J Neurol. 1989 Jan;236(1):4-8. doi: 10.1007/BF00314209. J Neurol. 1989. PMID: 2915225

5

Proton magnetic resonance spectroscopy and intracranial tumours: clinical perspectives.

Falini A, Calabrese G, Origgi D, Lipari S, Triulzi F, Losa M, Scotti G. Falini A, et al. Among authors: triulzi f. J Neurol. 1996 Oct;243(10):706-14. doi: 10.1007/BF00873976. J Neurol. 1996. PMID: 8923303

6

Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment.

Zucca C, Binda S, Borgatti R, Triulzi F, Radice L, Buttè C, Barkhaus PE, Barbi M. Zucca C, et al. Among authors: triulzi f. Neurology. 2003 Sep 9;61(5):710-2. doi: 10.1212/wnl.61.5.710. Neurology. 2003. PMID: 12963772

7

A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance.

Romaniello R, Tonelli A, Arrigoni F, Baschirotto C, Triulzi F, Bresolin N, Bassi MT, Borgatti R. Romaniello R, et al. Among authors: triulzi f. Dev Med Child Neurol. 2012 Aug;54(8):765-9. doi: 10.1111/j.1469-8749.2012.04316.x. Epub 2012 May 16. Dev Med Child Neurol. 2012. PMID: 22591407 Free article.

8

Cerebroretinal microangiopathy with calcifications and cysts associated with CTC1 and NDP mutations.

Romaniello R, Arrigoni F, Citterio A, Tonelli A, Sforzini C, Rizzari C, Pessina M, Triulzi F, Bassi MT, Borgatti R. Romaniello R, et al. Among authors: triulzi f. J Child Neurol. 2013 Dec;28(12):1702-8. doi: 10.1177/0883073812467849. Epub 2012 Dec 5. J Child Neurol. 2013. PMID: 23220793

9

Brain malformations and mutations in α- and β-tubulin genes: a review of the literature and description of two new cases.

Romaniello R, Arrigoni F, Cavallini A, Tenderini E, Baschirotto C, Triulzi F, Bassi MT, Borgatti R. Romaniello R, et al. Among authors: triulzi f. Dev Med Child Neurol. 2014 Apr;56(4):354-60. doi: 10.1111/dmcn.12370. Epub 2014 Jan 7. Dev Med Child Neurol. 2014. PMID: 24392928 Free article. Review.

10

Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum.

Romaniello R, Marelli S, Giorda R, Bedeschi MF, Bonaglia MC, Arrigoni F, Triulzi F, Bassi MT, Borgatti R. Romaniello R, et al. Among authors: triulzi f. J Child Neurol. 2017 Jan;32(1):60-71. doi: 10.1177/0883073816664668. Epub 2016 Sep 29. J Child Neurol. 2017. PMID: 27683483

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