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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: giovagnoli ar. Neurology. 2014 Sep 9;83(11):981-9. doi: 10.1212/WNL.0000000000000770. Epub 2014 Aug 6. Neurology. 2014. PMID: 25098542
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.
Bugiani O, Giaccone G, Rossi G, Mangieri M, Capobianco R, Morbin M, Mazzoleni G, Cupidi C, Marcon G, Giovagnoli A, Bizzi A, Di Fede G, Puoti G, Carella F, Salmaggi A, Romorini A, Patruno GM, Magoni M, Padovani A, Tagliavini F. Bugiani O, et al. Arch Neurol. 2010 Aug;67(8):987-95. doi: 10.1001/archneurol.2010.178. Arch Neurol. 2010. PMID: 20697050
Selective theory of mind impairment and cerebellar atrophy: a case report.
Parente A, Manfredi V, Tarallo A, Salsano E, Erbetta A, Pareyson D, Giovagnoli AR. Parente A, et al. Among authors: giovagnoli ar. J Neurol. 2013 Aug;260(8):2166-9. doi: 10.1007/s00415-013-6985-0. Epub 2013 Jun 16. J Neurol. 2013. PMID: 23771507 No abstract available.
104 results