Farina L - Search Results

1

Wallerian degeneration of the pontocerebellar fibers.

De Simone T, Regna-Gladin C, Carriero MR, Farina L, Savoiardo M. De Simone T, et al. Among authors: farina l. AJNR Am J Neuroradiol. 2005 May;26(5):1062-5. AJNR Am J Neuroradiol. 2005. PMID: 15891160 Free PMC article.

2

The effects of wallerian degeneration of the optic radiations demonstrated by MRI.

Savoiardo M, Pareyson D, Grisoli M, Forester M, D'Incerti L, Farina L. Savoiardo M, et al. Among authors: farina l. Neuroradiology. 1992;34(4):323-5. doi: 10.1007/BF00588192. Neuroradiology. 1992. PMID: 1528444

3

Ganglioneuroblastoma of the spinal cord.

Sibilla L, Martelli A, Farina L, Uggetti C, Zappoli F, Sessa F, Rodriguez y Baena R, Gaeltani P. Sibilla L, et al. Among authors: farina l. AJNR Am J Neuroradiol. 1995 Apr;16(4 Suppl):875-7. AJNR Am J Neuroradiol. 1995. PMID: 7611061 Free PMC article.

4

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: farina l. Neuroradiology. 1998 Nov;40(11):727-33. doi: 10.1007/s002340050673. Neuroradiology. 1998. PMID: 9860123

5

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. Neuroradiology. 1998 Dec;40(12):807-11. doi: 10.1007/s002340050689. Neuroradiology. 1998. PMID: 9877136

6

Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria.

Nardocci N, Zorzi G, Farina L, Binelli S, Scaioli W, Ciano C, Verga L, Angelini L, Savoiardo M, Bugiani O. Nardocci N, et al. Among authors: farina l. Neurology. 1999 Apr 22;52(7):1472-8. doi: 10.1212/wnl.52.7.1472. Neurology. 1999. PMID: 10227637

7

Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients.

Farina L, Nardocci N, Bruzzone MG, D'Incerti L, Zorzi G, Verga L, Morbin M, Savoiardo M. Farina L, et al. Neuroradiology. 1999 May;41(5):376-80. doi: 10.1007/s002340050768. Neuroradiology. 1999. PMID: 10379598

8

MR imaging and proton MR spectroscopy in adult Krabbe disease.

Farina L, Bizzi A, Finocchiaro G, Pareyson D, Sghirlanzoni A, Bertagnolio B, Savoiardo M, Naidu S, Singhal BS, Wenger DA. Farina L, et al. AJNR Am J Neuroradiol. 2000 Sep;21(8):1478-82. AJNR Am J Neuroradiol. 2000. PMID: 11003282 Free PMC article.

9

Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease.

Selleri S, Torchiana E, Pareyson D, Lulli L, Bertagnolio B, Savoiardo M, Farina L, Carrara F, Filocamo M, Gatti R, Sghirlanzoni A, Uziel G, Finocchiaro G. Selleri S, et al. Among authors: farina l. J Neurol. 2000 Nov;247(11):875-7. doi: 10.1007/s004150070076. J Neurol. 2000. PMID: 11151421 No abstract available.

10

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: farina l. Neurology. 2001 May 22;56(10):1340-6. doi: 10.1212/wnl.56.10.1340. Neurology. 2001. PMID: 11376185

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