Farina L - Search Results

1

Hypomyelinating leukodystrophies in adults: Clinical and genetic features.

Di Bella D, Magri S, Benzoni C, Farina L, Maccagnano C, Sarto E, Moscatelli M, Baratta S, Ciano C, Piacentini SHMJ, Draghi L, Mauro E, Pareyson D, Gellera C, Taroni F, Salsano E. Di Bella D, et al. Among authors: farina l. Eur J Neurol. 2021 Mar;28(3):934-944. doi: 10.1111/ene.14646. Epub 2020 Dec 3. Eur J Neurol. 2021. PMID: 33190326

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

Familial schizencephaly associated with EMX2 mutation.

Granata T, Farina L, Faiella A, Cardini R, D'Incerti L, Boncinelli E, Battaglia G. Granata T, et al. Among authors: farina l. Neurology. 1997 May;48(5):1403-6. doi: 10.1212/wnl.48.5.1403. Neurology. 1997. PMID: 9153481

4

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

5

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

6

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.

7

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.

8

Positive response to immunomodulatory therapy in an adult patient with Rasmussen's encephalitis.

Villani F, Spreafico R, Farina L, Giovagnoli AR, Bernasconi P, Granata T, Avanzini G. Villani F, et al. Among authors: farina l. Neurology. 2001 Jan 23;56(2):248-50. doi: 10.1212/wnl.56.2.248. Neurology. 2001. PMID: 11160964

9

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

10

Spinal radiological findings in nine patients with spontaneous intracranial hypotension.

Chiapparini L, Farina L, D'Incerti L, Erbetta A, Pareyson D, CarrieroM R, Savoiardo M. Chiapparini L, et al. Among authors: farina l. Neuroradiology. 2002 Feb;44(2):143-50; discussion 151-2. doi: 10.1007/s002340100685. Neuroradiology. 2002. PMID: 11942367

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

433 results

Search Page