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Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study.
Federico A, Dotti MT, Cardaioli E, Grieco G, Malandrini A, Manneschi L, Plewnia K, Rufa A, Renieri A, Bruttini M, Perticoni GF. Federico A, et al. Among authors: cardaioli e. J Submicrosc Cytol Pathol. 1998 Oct;30(4):521-6. J Submicrosc Cytol Pathol. 1998. PMID: 9851061
Genetic leukoencephalopathies with unknown metabolic pathogenesis.
Federico A, Rufa A, Battisti C, Bianchi S, Cardaioli E, Da Pozzo P, De Stefano N, Formichi P, Sicurelli F, Dotti MT. Federico A, et al. Among authors: cardaioli e. Neurol Sci. 2001 Nov;22 Suppl 2:S108-12. doi: 10.1007/s100720100046. Neurol Sci. 2001. PMID: 11794472 Review.
54 results