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145 results

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Page 1
Brain fluorodeoxyglucose PET in adrenoleukodystrophy.
Salsano E, Marotta G, Manfredi V, Giovagnoli AR, Farina L, Savoiardo M, Pareyson D, Benti R, Uziel G. Salsano E, et al. Among authors: savoiardo m. Neurology. 2014 Sep 9;83(11):981-9. doi: 10.1212/WNL.0000000000000770. Epub 2014 Aug 6. Neurology. 2014. PMID: 25098542
Adult-onset leukodystrophies from respiratory chain disorders: do they exist?
Salsano E, Farina L, Lamperti C, Piscosquito G, Salerno F, Morandi L, Carrara F, Lamantea E, Zeviani M, Uziel G, Savoiardo M, Pareyson D. Salsano E, et al. Among authors: savoiardo m. J Neurol. 2013 Jun;260(6):1617-23. doi: 10.1007/s00415-013-6844-z. Epub 2013 Jan 29. J Neurol. 2013. PMID: 23358625 Review.
Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation.
Di Bella D, Pareyson D, Savoiardo M, Farina L, Ciano C, Caldarazzo S, Sagnelli A, Bonato S, Nava S, Bresolin N, Tedeschi G, Taroni F, Salsano E. Di Bella D, et al. Among authors: savoiardo m. Neurology. 2014 Sep 23;83(13):1217-8. doi: 10.1212/WNL.0000000000000812. Epub 2014 Aug 15. Neurology. 2014. PMID: 25128180 Free article. No abstract available.
Epileptic phenotypes associated with mitochondrial disorders.
Canafoglia L, Franceschetti S, Antozzi C, Carrara F, Farina L, Granata T, Lamantea E, Savoiardo M, Uziel G, Villani F, Zeviani M, Avanzini G. Canafoglia L, et al. Among authors: savoiardo m. Neurology. 2001 May 22;56(10):1340-6. doi: 10.1212/wnl.56.10.1340. Neurology. 2001. PMID: 11376185
CT and MRI in maple syrup urine disease.
Uziel G, Savoiardo M, Nardocci N. Uziel G, et al. Among authors: savoiardo m. Neurology. 1988 Mar;38(3):486-8. doi: 10.1212/wnl.38.3.486. Neurology. 1988. PMID: 3347354
Spontaneous intracranial hypotension with deep brain swelling.
Savoiardo M, Minati L, Farina L, De Simone T, Aquino D, Mea E, Filippini G, Bussone G, Chiapparini L. Savoiardo M, et al. Brain. 2007 Jul;130(Pt 7):1884-93. doi: 10.1093/brain/awm101. Epub 2007 May 29. Brain. 2007. PMID: 17535837
Novel (ovario) leukodystrophy related to AARS2 mutations.
Dallabona C, Diodato D, Kevelam SH, Haack TB, Wong LJ, Salomons GS, Baruffini E, Melchionda L, Mariotti C, Strom TM, Meitinger T, Prokisch H, Chapman K, Colley A, Rocha H, Ounap K, Schiffmann R, Salsano E, Savoiardo M, Hamilton EM, Abbink TE, Wolf NI, Ferrero I, Lamperti C, Zeviani M, Vanderver A, Ghezzi D, van der Knaap MS. Dallabona C, et al. Among authors: savoiardo m. Neurology. 2014 Jun 10;82(23):2063-71. doi: 10.1212/WNL.0000000000000497. Epub 2014 May 7. Neurology. 2014. PMID: 24808023 Free PMC article.
MRI in Leigh syndrome with SURF1 gene mutation.
Savoiardo M, Zeviani M, Uziel G, Farina L. Savoiardo M, et al. Ann Neurol. 2002 Jan;51(1):138-9. doi: 10.1002/ana.10031. Ann Neurol. 2002. PMID: 11782998 No abstract available.
145 results