De Stefano N - Search Results

1

Vitamin D levels in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Carluccio MA, Di Donato I, Pescini F, Battaglini M, Bianchi S, Valenti R, Nannucci S, Franci B, Stromillo ML, De Stefano N, Inzitari D, Pantoni L, Nuti R, Federico A, Gonnelli S, Dotti MT. Carluccio MA, et al. Among authors: de stefano n. Neurol Sci. 2017 Jul;38(7):1333-1336. doi: 10.1007/s10072-017-2900-2. Epub 2017 Apr 4. Neurol Sci. 2017. PMID: 28378255

2

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

3

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

4

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

5

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

6

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

7

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

8

Merosin positive congenital muscular dystrophy with severe involvement of the central nervous system.

De Stefano N, Dotti MT, Villanova M, Scarano G, Federico A. De Stefano N, et al. Brain Dev. 1996 Jul-Aug;18(4):323-6. doi: 10.1016/0387-7604(96)00029-0. Brain Dev. 1996. PMID: 8879654

9

A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case.

Plewnia K, Dotti MT, Malandrini A, Manneschi L, Battisti C, De Stefano N, Rufa A, Motolese E, Federico A. Plewnia K, et al. Among authors: de stefano n. J Submicrosc Cytol Pathol. 1997 Jul;29(3):335-8. J Submicrosc Cytol Pathol. 1997. PMID: 9267042

10

New perspectives in clinical neurology: the promise of non-conventional magnetic resonance techniques.

Federico A, De Stefano N. Federico A, et al. Among authors: de stefano n. Ital J Neurol Sci. 1997 Dec;18(6):319-20. doi: 10.1007/BF02048234. Ital J Neurol Sci. 1997. PMID: 9494863 No abstract available.

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