Dotti MT - Search Results

1

De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalities.

Battisti C, Bonaglia MC, Giglio S, Anichini C, Pucci L, Dotti MT, Zuffardi O, Federico A. Battisti C, et al. Among authors: dotti mt. Am J Med Genet A. 2003 Mar 15;117A(3):207-11. doi: 10.1002/ajmg.a.10149. Am J Med Genet A. 2003. PMID: 12599183

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

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

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

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

9

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. Among authors: dotti mt. Neuropediatrics. 1988 May;19(2):109-12. doi: 10.1055/s-2008-1052412. Neuropediatrics. 1988. PMID: 3374764

10

Familial acute dystonic-dyskinetic syndrome with dominant inheritance after use of antidopaminergic antiemetic drugs.

Macucci M, Dotti MT, Federico A. Macucci M, et al. Among authors: dotti mt. Mov Disord. 1995 Jul;10(4):528-9. Mov Disord. 1995. PMID: 7565844 No abstract available.

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