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Page 1
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia.
Virgilio R, Ronchi D, Hadjigeorgiou GM, Bordoni A, Saladino F, Moggio M, Adobbati L, Kafetsouli D, Tsironi E, Previtali S, Papadimitriou A, Bresolin N, Comi GP. Virgilio R, et al. Among authors: adobbati l. J Neurol. 2008 Sep;255(9):1384-91. doi: 10.1007/s00415-008-0926-3. Epub 2008 Jun 30. J Neurol. 2008. PMID: 18575922
Cytochrome c oxidase during human fetal development.
Moggio M, Bresolin N, Scarpini E, Adobbati L, Prelle A, Gallanti A, Bet L, Fortunato F, Pellegrini G, Scarlato G. Moggio M, et al. Among authors: adobbati l. Int J Dev Neurosci. 1989;7(1):5-14. doi: 10.1016/0736-5748(89)90040-3. Int J Dev Neurosci. 1989. PMID: 2540623
Muscle glucose-6-phosphate dehydrogenase deficiency.
Bresolin N, Bet L, Moggio M, Meola G, Fortunato F, Comi G, Adobbati L, Geremia L, Pittalis S, Scarlato G. Bresolin N, et al. Among authors: adobbati l. J Neurol. 1989 May;236(4):193-8. doi: 10.1007/BF00314498. J Neurol. 1989. PMID: 2760630
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation.
Sciacco M, Prelle A, Comi GP, Napoli L, Battistel A, Bresolin N, Tancredi L, Lamperti C, Bordoni A, Fagiolari G, Ciscato P, Chiveri L, Perini MP, Fortunato F, Adobbati L, Messina S, Toscano A, Martinelli-Boneschi F, Papadimitriou A, Scarlato G, Moggio M. Sciacco M, et al. Among authors: adobbati l. J Neurol. 2001 Sep;248(9):778-88. doi: 10.1007/s004150170094. J Neurol. 2001. PMID: 11596783
20 results