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Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.
Santorelli FM, Sciacco M, Tanji K, Shanske S, Vu TH, Golzi V, Griggs RC, Mendell JR, Hays AP, Bertorini TE, Pestronk A, Bonilla E, DiMauro S. Santorelli FM, et al. Ann Neurol. 1996 Jun;39(6):789-95. doi: 10.1002/ana.410390615. Ann Neurol. 1996. PMID: 8651651
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle.
Prelle A, Rigoletto C, Moggio M, Sciacco M, Comi GP, Ciscato P, Fagiolari G, Rapuzzi S, Bignotti V, Scarlato G. Prelle A, et al. J Neurol Sci. 1996 Sep 1;140(1-2):132-6. doi: 10.1016/0022-510x(96)00129-3. J Neurol Sci. 1996. PMID: 8866439
Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.
Comi GP, Bordoni A, Salani S, Franceschina L, Sciacco M, Prelle A, Fortunato F, Zeviani M, Napoli L, Bresolin N, Moggio M, Ausenda CD, Taanman JW, Scarlato G. Comi GP, et al. Ann Neurol. 1998 Jan;43(1):110-6. doi: 10.1002/ana.410430119. Ann Neurol. 1998. PMID: 9450776
Clinical manifestations of mitochondrial DNA depletion.
Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.
Papadimitriou A, Comi GP, Hadjigeorgiou GM, Bordoni A, Sciacco M, Napoli L, Prelle A, Moggio M, Fagiolari G, Bresolin N, Salani S, Anastasopoulos I, Giassakis G, Divari R, Scarlato G. Papadimitriou A, et al. Neurology. 1998 Oct;51(4):1086-92. doi: 10.1212/wnl.51.4.1086. Neurology. 1998. PMID: 9781534
A novel mitochondrial tRNA(Ile) point mutation in chronic progressive external ophthalmoplegia.
Franceschina L, Salani S, Bordoni A, Sciacco M, Napoli L, Comi GP, Prelle A, Fortunato F, Hadjigeorgiou GM, Farina E, Bresolin N, D'Angelo MG, Scarlato G. Franceschina L, et al. J Neurol. 1998 Nov;245(11):755-8. doi: 10.1007/s004150050283. J Neurol. 1998. PMID: 9808249 No abstract available.
Lack of apoptosis in mitochondrial encephalomyopathies.
Sciacco M, Fagiolari G, Lamperti C, Messina S, Bazzi P, Napoli L, Chiveri L, Prelle A, Comi GP, Bresolin N, Scarlato G, Moggio M. Sciacco M, et al. Neurology. 2001 Apr 24;56(8):1070-4. doi: 10.1212/wnl.56.8.1070. Neurology. 2001. PMID: 11320180
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. J Neurol. 2001 Sep;248(9):778-88. doi: 10.1007/s004150170094. J Neurol. 2001. PMID: 11596783
A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family.
Napoli L, Bordoni A, Zeviani M, Hadjigeorgiou GM, Sciacco M, Tiranti V, Terentiou A, Moggio M, Papadimitriou A, Scarlato G, Comi GP. Napoli L, et al. Neurology. 2001 Dec 26;57(12):2295-8. doi: 10.1212/wnl.57.12.2295. Neurology. 2001. PMID: 11756613
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