Scaravilli F - Search Results

1

A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation.

Howard RS, Greenwood R, Gawler J, Scaravilli F, Marsden CD, Harding AE. Howard RS, et al. Among authors: scaravilli f. J Neurol Neurosurg Psychiatry. 1993 Sep;56(9):977-81. doi: 10.1136/jnnp.56.9.977. J Neurol Neurosurg Psychiatry. 1993. PMID: 8410038 Free PMC article.

2

Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adults.

Harding BN, Alsanjari N, Smith SJ, Wiles CM, Thrush D, Miller DH, Scaravilli F, Harding AE. Harding BN, et al. Among authors: scaravilli f. J Neurol Neurosurg Psychiatry. 1995 Mar;58(3):320-5. doi: 10.1136/jnnp.58.3.320. J Neurol Neurosurg Psychiatry. 1995. PMID: 7897414 Free PMC article. Review.

3

Nigral degeneration in neuroacanthocytosis.

Rinne JO, Daniel SE, Scaravilli F, Harding AE, Marsden CD. Rinne JO, et al. Among authors: scaravilli f. Neurology. 1994 Sep;44(9):1629-32. doi: 10.1212/wnl.44.9.1629. Neurology. 1994. PMID: 7936287

4

Bilateral symmetrical enhancing brainstem lesions: an unusual presentation of primary CNS lymphoma.

Larner AJ, D'Arrigo C, Scaravilli F, Howard RS. Larner AJ, et al. Among authors: scaravilli f. Eur J Neurol. 1999 Nov;6(6):721-3. doi: 10.1046/j.1468-1331.1999.660721.x. Eur J Neurol. 1999. PMID: 10529762

5

The neuropathological features of neuroacanthocytosis.

Rinne JO, Daniel SE, Scaravilli F, Pires M, Harding AE, Marsden CD. Rinne JO, et al. Among authors: scaravilli f. Mov Disord. 1994 May;9(3):297-304. doi: 10.1002/mds.870090303. Mov Disord. 1994. PMID: 8041370 Review.

6

Corticobasal degeneration look-alikes.

Bhatia KP, Lee MS, Rinne JO, Revesz T, Scaravilli F, Davies L, Marsden CD. Bhatia KP, et al. Among authors: scaravilli f. Adv Neurol. 2000;82:169-82. Adv Neurol. 2000. PMID: 10624481 Review. No abstract available.

7

Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.

Baraitser M, Gooddy W, Halliday AM, Harding AE, Rudge P, Scaravilli F. Baraitser M, et al. Among authors: scaravilli f. J Neurol Neurosurg Psychiatry. 1984 Jan;47(1):21-5. doi: 10.1136/jnnp.47.1.21. J Neurol Neurosurg Psychiatry. 1984. PMID: 6319613 Free PMC article.

8

A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic study.

Nelson I, Hanna MG, Alsanjari N, Scaravilli F, Morgan-Hughes JA, Harding AE. Nelson I, et al. Among authors: scaravilli f. Ann Neurol. 1995 Mar;37(3):400-3. doi: 10.1002/ana.410370317. Ann Neurol. 1995. PMID: 7695240

9

A follow-up study of isolated cases of suspected Huntington's disease.

Bateman D, Boughey AM, Scaravilli F, Marsden CD, Harding AE. Bateman D, et al. Among authors: scaravilli f. Ann Neurol. 1992 Mar;31(3):293-8. doi: 10.1002/ana.410310311. Ann Neurol. 1992. PMID: 1386209 Review.

10

Hemiballism and chorea in a patient with parkinsonism due to a multisystem degeneration.

Steiger MJ, Pires M, Scaravilli F, Quinn NP, Marsden CD. Steiger MJ, et al. Among authors: scaravilli f. Mov Disord. 1992;7(1):71-7. doi: 10.1002/mds.870070115. Mov Disord. 1992. PMID: 1557069

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