Dotti MT - Search Results

1

A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient.

Pescini F, Bianchi S, Salvadori E, Poggesi A, Dotti MT, Federico A, Inzitari D, Pantoni L. Pescini F, et al. Among authors: dotti mt. J Neurol Sci. 2008 Apr 15;267(1-2):170-3. doi: 10.1016/j.jns.2007.10.017. Epub 2007 Nov 19. J Neurol Sci. 2008. PMID: 18022198

2

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

3

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

4

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.

5

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

6

Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generations.

Mangano L, Palmeri S, Dotti MT, Moschini F, Federico A. Mangano L, et al. Among authors: dotti mt. Am J Med Genet. 1989 Jan;32(1):67-71. doi: 10.1002/ajmg.1320320115. Am J Med Genet. 1989. PMID: 2705485

7

Mitochondrial enzyme deficiency in cerebrotendinous xanthomatosis.

Dotti MT, Manneschi L, Federico A. Dotti MT, et al. J Neurol Sci. 1995 Apr;129(2):106-8. doi: 10.1016/0022-510x(94)00256-n. J Neurol Sci. 1995. PMID: 7608723

8

Amiodarone-induced parkinsonism: a case report and pathogenetic discussion.

Dotti MT, Federico A. Dotti MT, et al. Mov Disord. 1995 Mar;10(2):233-4. doi: 10.1002/mds.870100223. Mov Disord. 1995. PMID: 7753074 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. AJNR Am J Neuroradiol. 1994 Oct;15(9):1721-6. AJNR Am J Neuroradiol. 1994. PMID: 7847220 Free PMC article. Review.

10

Treatment of cerebrotendinous xanthomatosis.

Federico A, Dotti MT. Federico A, et al. Among authors: dotti mt. Neurology. 1994 Nov;44(11):2218. doi: 10.1212/wnl.44.11.2218. Neurology. 1994. PMID: 7970001 No abstract available.

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