Dotti MT - Search Results

1

CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients.

Bianchi S, Zicari E, Carluccio A, Di Donato I, Pescini F, Nannucci S, Valenti R, Ragno M, Inzitari D, Pantoni L, Federico A, Dotti MT. Bianchi S, et al. Among authors: dotti mt. J Neurol. 2015 Jan;262(1):134-41. doi: 10.1007/s00415-014-7533-2. Epub 2014 Oct 26. J Neurol. 2015. PMID: 25344745

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

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.

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

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

8

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

9

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

10

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

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