Farina L - Search Results

1

Forloni G, Iussich S, Awan T, Colombo L, Angeretti N, Girola L, Bertani I, Poli G, Caramelli M, Grazia Bruzzone M, Farina L, Limido L, Rossi G, Giaccone G, Ironside JW, Bugiani O, Salmona M, Tagliavini F. Forloni G, et al. Among authors: farina l. Proc Natl Acad Sci U S A. 2002 Aug 6;99(16):10849-54. doi: 10.1073/pnas.162195499. Epub 2002 Jul 29. Proc Natl Acad Sci U S A. 2002. PMID: 12149459 Free PMC article.

2

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

3

Familial frontotemporal dementia associated with the novel MAPT mutation T427M.

Giaccone G, Rossi G, Farina L, Marcon G, Di Fede G, Catania M, Morbin M, Sacco L, Bugiani O, Tagliavini F. Giaccone G, et al. Among authors: farina l. J Neurol. 2005 Dec;252(12):1543-5. doi: 10.1007/s00415-005-0879-8. Epub 2005 Jun 6. J Neurol. 2005. PMID: 15940384 No abstract available.

4

The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.

Rossi G, Marelli C, Farina L, Laurà M, Maria Basile A, Ciano C, Tagliavini F, Pareyson D. Rossi G, et al. Among authors: farina l. Mov Disord. 2008 Apr 30;23(6):892-5. doi: 10.1002/mds.21970. Mov Disord. 2008. PMID: 18307268

5

Prodromal Alzheimer's disease presenting as cerebral amyloid angiopathy-related inflammation with spontaneous amyloid-related imaging abnormalities and high cerebrospinal fluid anti-Aβ autoantibodies.

Boncoraglio GB, Piazza F, Savoiardo M, Farina L, DiFrancesco JC, Prioni S, Tagliavini F, Parati EA, Giaccone G. Boncoraglio GB, et al. Among authors: farina l. J Alzheimers Dis. 2015;45(2):363-7. doi: 10.3233/JAD-142376. J Alzheimers Dis. 2015. PMID: 25537009

6

Unusual presentations and intrafamilial phenotypic variability in infantile onset Alexander disease.

Tonduti D, Ardissone A, Ceccherini I, Giaccone G, Farina L, Moroni I. Tonduti D, et al. Among authors: farina l. Neurol Sci. 2016 Jun;37(6):973-7. doi: 10.1007/s10072-015-2466-9. Epub 2016 Jan 7. Neurol Sci. 2016. PMID: 26743065

7

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

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

9

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

10

Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities.

Mora M, Moroni I, Uziel G, di Blasi C, Barresi R, Farina L, Morandi L. Mora M, et al. Among authors: farina l. Neuromuscul Disord. 1996 Oct;6(5):377-81. doi: 10.1016/0960-8966(96)00359-8. Neuromuscul Disord. 1996. PMID: 8938702

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