De Stefano N - Search Results

1

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

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

Cherry-red spot myoclonus syndrome (type I sialidosis).

Federico A, Battistini S, Ciacci G, de Stefano N, Gatti R, Durand P, Guazzi GC. Federico A, et al. Among authors: de stefano n. Dev Neurosci. 1991;13(4-5):320-6. doi: 10.1159/000112180. Dev Neurosci. 1991. PMID: 1817038 Review.

4

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

5

Serum vitamin E in inherited ataxias.

Eusebi MP, Battisti C, De Stefano N, De Michele G, Filla A, Federico A. Eusebi MP, et al. Among authors: de michele g, de stefano n. Acta Neurol (Napoli). 1990 Apr;12(2):147-50. Acta Neurol (Napoli). 1990. PMID: 2360480

6

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.

7

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

8

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

9

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

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

471 results

Search Page

Filters