Savasta SM - Search Results

1

Pelizaeus-Merzbacher disease: electrophysiological study of two sibs with the classic form and of their relatives.

Alfonsi E, Clerici AM, Costi I, Berardinelli A, Rognone F, Savasta SM, Moglia A. Alfonsi E, et al. Among authors: savasta sm. Funct Neurol. 2001 Oct-Dec;16(4):337-45. Funct Neurol. 2001. PMID: 11853325

2

Kikuchi-Fujimoto disease complicated by peripheral neuropathy.

Longaretti P, Savasta S, Caimmi D, Possenti I, Marseglia GL. Longaretti P, et al. Pediatr Neurol. 2012 May;46(5):319-21. doi: 10.1016/j.pediatrneurol.2012.02.024. Pediatr Neurol. 2012. PMID: 22520354

3

Bickerstaff Brainstem Encephalitis and overlapping Guillain-Barré syndrome in children: Report of two cases and review of the literature.

Michev A, Musso P, Foiadelli T, Trabatti C, Lozza A, Franciotta D, Simoncelli AM, Savasta S. Michev A, et al. Eur J Paediatr Neurol. 2019 Jan;23(1):43-52. doi: 10.1016/j.ejpn.2018.11.008. Epub 2018 Nov 20. Eur J Paediatr Neurol. 2019. PMID: 30502045 Review.

4

Cell-based assays for the detection of MOG antibodies: a comparative study.

Gastaldi M, Scaranzin S, Jarius S, Wildeman B, Zardini E, Mallucci G, Rigoni E, Vegezzi E, Foiadelli T, Savasta S, Banfi P, Versino M, Benedetti L, Novi G, Mancardi MM, Giacomini T, Annovazzi P, Baroncini D, Ferraro D, Lampasona V, Reindl M, Waters P, Franciotta D. Gastaldi M, et al. J Neurol. 2020 Dec;267(12):3555-3564. doi: 10.1007/s00415-020-10024-0. Epub 2020 Jul 4. J Neurol. 2020. PMID: 32623596

5

Infantile mitochondria encephalomyopathies: report on 4 cases.

Pastoris O, Dossena M, Scelsi R, Savasta S, Bianchi E. Pastoris O, et al. Eur Neurol. 1993;33(1):54-61. doi: 10.1159/000116902. Eur Neurol. 1993. PMID: 8440289

6

Subependymal periventricular heterotopias in a patient with ehlers-danlos syndrome: a new case.

Savasta S, Crispino M, Valli M, Calligaro A, Zambelloni C, Poggiani C. Savasta S, et al. J Child Neurol. 2007 Mar;22(3):317-20. doi: 10.1177/0883073807299857. J Child Neurol. 2007. PMID: 17621503

7

Mitochondrial DNA deletion in a child with mitochondrial encephalomyopathy, growth hormone deficiency, and hypoparathyroidism.

Cassandrini D, Savasta S, Bozzola M, Tessa A, Pedemonte M, Assereto S, Stringara S, Minetti C, Santorelli FM, Bruno C. Cassandrini D, et al. J Child Neurol. 2006 Nov;21(11):983-5. doi: 10.1177/08830738060210111001. J Child Neurol. 2006. PMID: 17092469

8

Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

Verrotti A, Cusmai R, Laino D, Carotenuto M, Esposito M, Falsaperla R, Margari L, Rizzo R, Savasta S, Grosso S, Striano P, Belcastro V, Franzoni E, Curatolo P, Giordano L, Freri E, Matricardi S, Pruna D, Toldo I, Tozzi E, Lobefalo L, Operto F, Altobelli E, Chiarelli F, Spalice A. Verrotti A, et al. J Neurol. 2015 Jan;262(1):116-23. doi: 10.1007/s00415-014-7542-1. Epub 2014 Oct 18. J Neurol. 2015. PMID: 25326049

9

Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency.

Savasta S, Comi GP, Perini MP, Lupi A, Strazzer S, Rognoni F, Rossoni R. Savasta S, et al. J Child Neurol. 2001 Aug;16(8):608-13. doi: 10.1177/088307380101600816. J Child Neurol. 2001. PMID: 11510937

10

Long-term follow-up in children with benign convulsions associated with gastroenteritis.

Verrotti A, Moavero R, Vigevano F, Cantonetti L, Guerra A, Spezia E, Tricarico A, Nanni G, Agostinelli S, Chiarelli F, Parisi P, Capovilla G, Beccaria F, Spalice A, Coppola G, Franzoni E, Gentile V, Casellato S, Veggiotti P, Malgesini S, Crichiutti G, Balestri P, Grosso S, Zamponi N, Incorpora G, Savasta S, Costa P, Pruna D, Cusmai R. Verrotti A, et al. Eur J Paediatr Neurol. 2014 Sep;18(5):572-7. doi: 10.1016/j.ejpn.2014.04.006. Epub 2014 Apr 14. Eur J Paediatr Neurol. 2014. PMID: 24780603

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