Dotti MT - Search Results

1

Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis.

Malandrini A, Gambelli S, Muglia M, Berti G, Gaudiano C, Patitucci A, Sugie K, Umehara F, Quattrone A, Dotti MT, Federico A. Malandrini A, et al. Among authors: dotti mt. Brain Dev. 2008 Apr;30(4):291-4. doi: 10.1016/j.braindev.2007.07.010. Epub 2007 Sep 4. Brain Dev. 2008. PMID: 17768021

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

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

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

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.

9

Histochemical, ultrastructural and biochemical study of muscle mitochondria in Leber's hereditary optic atrophy.

Federico A, Manneschi L, Meloni M, Alessandrini C, Bardelli AM, Dotti MT, Sabatelli P. Federico A, et al. Among authors: dotti mt. J Inherit Metab Dis. 1988;11 Suppl 2:193-7. doi: 10.1007/BF01804233. J Inherit Metab Dis. 1988. PMID: 2846962 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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