Federico A - Search Results

1

Cerebro-ocular dysplasia and muscular dystrophy: report of two cases.

Federico A, Dotti MT, Malandrini A, Guazzi GC, Hayek G, Simonati A, Rizzuto N, Toti P. Federico A, et al. Neuropediatrics. 1988 May;19(2):109-12. doi: 10.1055/s-2008-1052412. Neuropediatrics. 1988. PMID: 3374764

2

Progressive myoclonus epilepsies. Criteria for diagnosis on the basis of the follow-up of 37 cases.

Guazzi GC, Federico A. Guazzi GC, et al. Among authors: federico a. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):469-84. Acta Neurol (Napoli). 1992. PMID: 1293989 Review.

3

Cerebrotendinous xanthomatosis as a multisystem disease mimicking premature ageing.

Dotti MT, Salen G, Federico A. Dotti MT, et al. Among authors: federico a. Dev Neurosci. 1991;13(4-5):371-6. doi: 10.1159/000112187. Dev Neurosci. 1991. PMID: 1817044 Review.

4

Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy.

Federico A, Dotti MT, Fabrizi GM, Palmeri S, Massimo L, Robinson BH, Malandrini A, Guazzi GC. Federico A, et al. Eur Neurol. 1990;30(3):123-7. doi: 10.1159/000117327. Eur Neurol. 1990. PMID: 2162773

5

Peripheral nerve involvement in ataxia telangiectasia: histological and ultrastructural studies of peroneal nerve biopsy in two cases.

Malandrini A, Guazzi GC, Alessandrini C, Federico A. Malandrini A, et al. Among authors: federico a. Clin Neuropathol. 1990 May-Jun;9(3):109-14. Clin Neuropathol. 1990. PMID: 2163784

6

Neurocutaneous syndromes with pigmentary abnormalities and central nervous system involvement. II. Two cases with atypical incontinentia pigmenti.

Federico A, Fabrizi GM, Dotti MT, Palmeri S, Aguglia U, Miracco C, Guazzi GC. Federico A, et al. Acta Neurol (Napoli). 1990 Aug;12(4):264-72. Acta Neurol (Napoli). 1990. PMID: 2251951

7

Infanto-juvenile encephaloneuropathy and pigmentary retinopathy in a girl associated with congenital adrenal insufficiency and altered plasma medium-chain fatty acid levels.

Federico A, Baracchini G, Dotti MT, Ibba L, Malandrini A, Ciacci G, Meloni M, Palmeri S, Pompella A, Guazzi GC. Federico A, et al. J Inherit Metab Dis. 1988;11 Suppl 2:178-82. doi: 10.1007/BF01804229. J Inherit Metab Dis. 1988. PMID: 2846958 No abstract available.

8

Adrenomyeloneurodystrophy with late cerebral involvement and evidence of a multiple autoimmune disorder.

Federico A, Dotti MT, Annunziata P, Bonuccelli U, Fenzi G, Ciacci G, Malandrini A, Meucci G, Guazzi GC. Federico A, et al. J Inherit Metab Dis. 1988;11 Suppl 2:169-72. doi: 10.1007/BF01804227. J Inherit Metab Dis. 1988. PMID: 3141701 No abstract available.

9

Cerebrotendinous xanthomatosis (van Bogaert-Scherer-Epstein disease): CT and MR findings.

Dotti MT, Federico A, Signorini E, Caputo N, Venturi C, Filosomi G, Guazzi GC. Dotti MT, et al. Among authors: federico a. AJNR Am J Neuroradiol. 1994 Oct;15(9):1721-6. AJNR Am J Neuroradiol. 1994. PMID: 7847220 Free PMC article. Review.

10

Association of myopathy with multiple exostoses and mental retardation: a case report.

De Stefano N, Dotti MT, Malandrini A, Federico A. De Stefano N, et al. Among authors: federico a. Brain Dev. 1994 Mar-Apr;16(2):136-8. doi: 10.1016/0387-7604(94)90050-7. Brain Dev. 1994. PMID: 8048702

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,184 results

Search Page

Filters