De Stefano N - Search Results

1

Evidence of early cortical atrophy in MS: relevance to white matter changes and disability.

De Stefano N, Matthews PM, Filippi M, Agosta F, De Luca M, Bartolozzi ML, Guidi L, Ghezzi A, Montanari E, Cifelli A, Federico A, Smith SM. De Stefano N, et al. Among authors: de luca m. Neurology. 2003 Apr 8;60(7):1157-62. doi: 10.1212/01.wnl.0000055926.69643.03. Neurology. 2003. PMID: 12682324 Clinical Trial.

2

Vitamin E deficiency secondary to chronic intestinal malabsorption and effect of vitamin supplement: a case report.

Federico A, Battisti C, Eusebi MP, de Stefano N, Malandrini A, Mondelli M, Volpi N. Federico A, et al. Among authors: de stefano n. Eur Neurol. 1991;31(6):366-71. doi: 10.1159/000116695. Eur Neurol. 1991. PMID: 1661677

3

Unexpected white matter changes in an early treated PKU case and improvement after dietary treatment.

Battistini S, De Stefano N, Parlanti S, Federico A. Battistini S, et al. Among authors: de stefano n. Funct Neurol. 1991 Apr-Jun;6(2):177-80. Funct Neurol. 1991. PMID: 1916459

4

Cerebral thromboangiitis obliterans: clinical and MRI findings in a case.

Dotti MT, De Stefano N, Vecchione V, Correra G, Federico A. Dotti MT, et al. Among authors: de stefano n. Eur Neurol. 1995;35(4):246-8. doi: 10.1159/000117142. Eur Neurol. 1995. PMID: 7671993 No abstract available.

5

Short-term dichloroacetate treatment improves indices of cerebral metabolism in patients with mitochondrial disorders.

De Stefano N, Matthews PM, Ford B, Genge A, Karpati G, Arnold DL. De Stefano N, et al. Neurology. 1995 Jun;45(6):1193-8. doi: 10.1212/wnl.45.6.1193. Neurology. 1995. PMID: 7783888 Clinical Trial.

6

Primary antiphospholipid syndrome: two case reports, one with histological examination of skin, peripheral nerve and muscle.

Macucci M, Dotti MT, Battistini S, De Stefano N, Vecchione V, Orefice G, Malandrini A, Federico A. Macucci M, et al. Among authors: de stefano n. Acta Neurol (Napoli). 1994 Jun;16(3):87-96. Acta Neurol (Napoli). 1994. PMID: 7992667

7

Association of myopathy with multiple exostoses and mental retardation: a case report.

De Stefano N, Dotti MT, Malandrini A, Federico A. De Stefano N, et al. Brain Dev. 1994 Mar-Apr;16(2):136-8. doi: 10.1016/0387-7604(94)90050-7. Brain Dev. 1994. PMID: 8048702

8

Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study.

Dotti MT, Manneschi L, Malandrini A, De Stefano N, Caznerale F, Federico A. Dotti MT, et al. Among authors: de stefano n. Brain Dev. 1993 Mar-Apr;15(2):103-6. doi: 10.1016/0387-7604(93)90045-a. Brain Dev. 1993. PMID: 8214327

9

Sensory-motor hereditary neuropathy with early onset. A case report.

Malandrini A, De Stefano N, Dotti MT, Vecchione V, Federico A. Malandrini A, et al. Among authors: de stefano n. Acta Neurol (Napoli). 1993 Apr;15(2):81-6. Acta Neurol (Napoli). 1993. PMID: 8328327

10

Optic atrophy in Marinesco-Sjögren syndrome: an additional ocular feature. Report of three cases in two families.

Dotti MT, Bardelli AM, De Stefano N, Federico A, Malandrini A, Vanni M, Guazzi GC. Dotti MT, et al. Among authors: de stefano n. Ophthalmic Paediatr Genet. 1993 Mar;14(1):5-7. doi: 10.3109/13816819309087616. Ophthalmic Paediatr Genet. 1993. PMID: 8345957

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