Dotti MT - Search Results

1

Evoked potentials in cerebrotendinous xanthomatosis and effect induced by chenodeoxycholic acid.

Mondelli M, Rossi A, Scarpini C, Dotti MT, Federico A. Mondelli M, et al. Among authors: dotti mt. Arch Neurol. 1992 May;49(5):469-75. doi: 10.1001/archneur.1992.00530290051011. Arch Neurol. 1992. PMID: 1316120

2

Magnetic resonance imaging findings in Leber's hereditary optic neuropathy.

Dotti MT, Caputo N, Signorini E, Federico A. Dotti MT, et al. Eur Neurol. 1992;32(1):17-9. doi: 10.1159/000116781. Eur Neurol. 1992. PMID: 1563448

3

Muscle mitochondrial changes in cerebrotendinous xanthomatosis.

Federico A, Dotti MT, Volpi N. Federico A, et al. Among authors: dotti mt. Ann Neurol. 1991 Nov;30(5):734-5. doi: 10.1002/ana.410300517. Ann Neurol. 1991. PMID: 1763899 No abstract available.

4

Leber's optic atrophy: VEP and BAEP changes in 16 asymptomatic subjects.

Mondelli M, Rossi A, Scarpini C, Dotti MT, Federico A. Mondelli M, et al. Among authors: dotti mt. Acta Neurol Scand. 1991 Oct;84(4):366. doi: 10.1111/j.1600-0404.1991.tb04970.x. Acta Neurol Scand. 1991. PMID: 1772010 No abstract available.

5

Cerebrotendinous xanthomatosis as a multisystem disease mimicking premature ageing.

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

6

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. Among authors: dotti mt. Eur Neurol. 1990;30(3):123-7. doi: 10.1159/000117327. Eur Neurol. 1990. PMID: 2162773

7

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. Among authors: dotti mt. Acta Neurol (Napoli). 1990 Aug;12(4):264-72. Acta Neurol (Napoli). 1990. PMID: 2251951

8

BAEP changes in Leber's hereditary optic atrophy: further confirmation of multisystem involvement.

Mondelli M, Rossi A, Scarpini C, Dotti MT, Federico A. Mondelli M, et al. Among authors: dotti mt. Acta Neurol Scand. 1990 Apr;81(4):349-53. doi: 10.1111/j.1600-0404.1990.tb01569.x. Acta Neurol Scand. 1990. PMID: 2360403

9

Atypical phenotype of Refsum's disease: clinical, biochemical, neurophysiological and pathological study.

Dotti MT, Rossi A, Rizzuto N, Hayek G, Bardelli N, Bardelli AM, Federico A. Dotti MT, et al. Eur Neurol. 1985;24(2):85-93. doi: 10.1159/000115767. Eur Neurol. 1985. PMID: 2579819

10

Congenital oculo-facial paralysis (Moebius syndrome): evidence of dominant inheritance in two families.

Dotti MT, Federico A, Palmeri S, Guazzi GC. Dotti MT, et al. Acta Neurol (Napoli). 1989 Dec;11(6):434-8. Acta Neurol (Napoli). 1989. PMID: 2618829

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

320 results

Search Page

Filters