Savoiardo M - Search Results

1

4-Hydroxybutyric aciduria: clinical findings and vigabatrin therapy.

Uziel G, Bardelli P, Pantaleoni C, Rimoldi M, Savoiardo M. Uziel G, et al. Among authors: savoiardo m. J Inherit Metab Dis. 1993;16(3):520-2. doi: 10.1007/BF00711670. J Inherit Metab Dis. 1993. PMID: 7609441 No abstract available.

2

L-2-Hydroxyglutaric aciduria: MRI in seven cases.

D'Incerti L, Farina L, Moroni I, Uziel G, Savoiardo M. D'Incerti L, et al. Among authors: savoiardo m. Neuroradiology. 1998 Nov;40(11):727-33. doi: 10.1007/s002340050673. Neuroradiology. 1998. PMID: 9860123

3

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

4

Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients.

Farina L, Morandi L, Milanesi I, Ciceri E, Mora M, Moroni I, Pantaleoni C, Savoiardo M. Farina L, et al. Among authors: savoiardo m. Neuroradiology. 1998 Dec;40(12):807-11. doi: 10.1007/s002340050689. Neuroradiology. 1998. PMID: 9877136

5

Hemophagocytic lymphohistiocytosis with neurological presentation: MRI findings and a nearly miss diagnosis.

Chiapparini L, Uziel G, Vallinoto C, Bruzzone MG, Rovelli A, Tricomi G, Bizzi A, Nardocci N, Rizzari C, Savoiardo M. Chiapparini L, et al. Among authors: savoiardo m. Neurol Sci. 2011 Jun;32(3):473-7. doi: 10.1007/s10072-010-0467-2. Epub 2011 Jan 14. Neurol Sci. 2011. PMID: 21234777

6

MR findings in Leigh syndrome with COX deficiency and SURF-1 mutations.

Farina L, Chiapparini L, Uziel G, Bugiani M, Zeviani M, Savoiardo M. Farina L, et al. Among authors: savoiardo m. AJNR Am J Neuroradiol. 2002 Aug;23(7):1095-100. AJNR Am J Neuroradiol. 2002. PMID: 12169463 Free PMC article.

7

Epilepsia partialis continua associated with NADH-coenzyme Q reductase deficiency.

Antozzi C, Franceschetti S, Filippini G, Barbiroli B, Savoiardo M, Fiacchino F, Rimoldi M, Lodi R, Zaniol P, Zeviani M. Antozzi C, et al. Among authors: savoiardo m. J Neurol Sci. 1995 Apr;129(2):152-61. doi: 10.1016/0022-510x(94)00267-r. J Neurol Sci. 1995. PMID: 7608730

8

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

9

Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series.

Prodi E, Grisoli M, Panzeri M, Minati L, Fattori F, Erbetta A, Uziel G, D'Arrigo S, Tessa A, Ciano C, Santorelli FM, Savoiardo M, Mariotti C. Prodi E, et al. Among authors: savoiardo m. Eur J Neurol. 2013 Jan;20(1):138-46. doi: 10.1111/j.1468-1331.2012.03815.x. Epub 2012 Jul 21. Eur J Neurol. 2013. PMID: 22816526

10

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

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