Farina L - Search Results

1

Can MR imaging diagnose adult-onset Alexander disease?

Farina L, Pareyson D, Minati L, Ceccherini I, Chiapparini L, Romano S, Gambaro P, Fancellu R, Savoiardo M. Farina L, et al. AJNR Am J Neuroradiol. 2008 Jun;29(6):1190-6. doi: 10.3174/ajnr.A1060. Epub 2008 Apr 3. AJNR Am J Neuroradiol. 2008. PMID: 18388212 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

Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositis.

Di Blasi C, Mora M, Pareyson D, Farina L, Sghirlanzoni A, Vignier N, Blasevich F, Cornelio F, Guicheney P, Morandi L. Di Blasi C, et al. Among authors: farina l. Ann Neurol. 2000 Jun;47(6):811-6. Ann Neurol. 2000. PMID: 10852549

9

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.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

434 results

Search Page