Dotti MT - Search Results

1

The first Italian family with tibial muscular dystrophy caused by a novel titin mutation.

Pollazzon M, Suominen T, Penttilä S, Malandrini A, Carluccio MA, Mondelli M, Marozza A, Federico A, Renieri A, Hackman P, Dotti MT, Udd B. Pollazzon M, et al. Among authors: dotti mt. J Neurol. 2010 Apr;257(4):575-9. doi: 10.1007/s00415-009-5372-3. Epub 2009 Nov 13. J Neurol. 2010. PMID: 19911250

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

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. Among authors: dotti mt. J Inherit Metab Dis. 1988;11 Suppl 2:178-82. doi: 10.1007/BF01804229. J Inherit Metab Dis. 1988. PMID: 2846958 No abstract available.

10

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. Among authors: dotti mt. J Inherit Metab Dis. 1988;11 Suppl 2:169-72. doi: 10.1007/BF01804227. J Inherit Metab Dis. 1988. PMID: 3141701 No abstract available.

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