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1991

Appearance and localization of dystrophin in normal human fetal muscle

Prelle, A., Chianese, L., Moggio, M., Gallanti, A., Sciacco, M., Checcarelli, N., Comi, G., Scarpini, E., Bonilla, E. & Scarlato, G., 1991, In : International Journal of Developmental Neuroscience. 9, 6, p. 607-612 6 p.

Research output: Contribution to journalArticle

1992

Desmin and Vimentin as markers of regeneration in muscle diseases

Gallanti, A., Prelle, A., Moggio, M., Ciscato, P., Checcarelli, N., Sciacco, M., Comini, A. & Scarlato, G., Dec 1992, In : Acta Neuropathologica. 85, 1, p. 88-92 5 p.

Research output: Contribution to journalArticle

Guillain-Barré syndrome associated with high titers of anti-GM1 antibodies

Nobile-Orazio, E., Carpo, M., Meucci, N., Grassi, M. P., Capitani, E., Sciacco, M., Mangoni, A. & Scarlato, G., 1992, In : Journal of the Neurological Sciences. 109, 2, p. 200-206 7 p.

Research output: Contribution to journalArticle

Lack of anionic phospholipid calcium binding sites in Duchenne muscular dystrophy

Moggio, M., Fagiolari, G., Prelle, A., Gallanti, A., Sciacco, M. & Scarlato, G., 1992, In : Muscle and Nerve. 15, 3, p. 325-331 7 p.

Research output: Contribution to journalArticle

New morphological approaches to the study of mitochondrial encephalomyopathies

Bonilla, E., Sciacco, M., Tanji, K., Sparaco, M., Petruzzella, V. & Moraes, C. T., 1992, In : Brain Pathology. 2, 2, p. 113-119 7 p.

Research output: Contribution to journalArticle

Sural nerve immunoreactivity for nerve growth factor receptor in a case of localized hypertrophic neuropathy

Sciacco, M., Scarpini, E., Baron, P. L., Doronzo, R., Moggio, M., Passerini, D. & Scarlato, G., Apr 1992, In : Acta Neuropathologica. 83, 5, p. 547-553 7 p.

Research output: Contribution to journalArticle

1993

Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA

Moraes, C. T., Ciacci, F., Silvestri, G., Shanske, S., Sciacco, M., Hirano, M., Schon, E. A., Bonilla, E. & DiMauro, S., 1993, In : Neuromuscular Disorders. 3, 1, p. 43-50 8 p.

Research output: Contribution to journalArticle

Decrease of nerve Na+,K+-ATPase activity in the pathogenesis of human diabetic neuropathy

Scarpini, E., Bianchi, R., Moggio, M., Sciacco, M., Fiori, M. G. & Scarlato, G., Dec 15 1993, In : Journal of the Neurological Sciences. 120, 2, p. 159-167 9 p.

Research output: Contribution to journalArticle

Immunolocalization of heat shock proteins in ragged-red fibers of patients with mitochondrial encephalomyopathies

Sparaco, M., Rosoklija, G., Tanji, K., Sciacco, M., Latov, N., DiMauro, S. & Bnilla, E., 1993, In : Neuromuscular Disorders. 3, 1, p. 71-76 6 p.

Research output: Contribution to journalArticle

1994

Anionic phospholipids calcium binding sites in Duchenne and murine x- linked muscular dystrophy

Moggio, M., Prelle, A., Fagiolari, G., Checcarelli, N., Sciacco, M., Ciscato, P. & Scarlato, G., 1994, In : Muscle and Nerve. 17, 5, p. 485-488 4 p.

Research output: Contribution to journalArticle

Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy

Sciacco, M., Bonilla, E., Schon, E. A., DiMauro, S. & Moraes, C. T., Jan 1994, In : Human Molecular Genetics. 3, 1, p. 13-19 7 p.

Research output: Contribution to journalArticle

1995

Paucity of deleted mitochondrial DNAs in brain regions of Huntington's disease patients

Chen, X., Bonilla, E., Sciacco, M. & Schon, E. A., May 24 1995, In : Biochimica et Biophysica Acta - Molecular Basis of Disease. 1271, 1, p. 229-233 5 p.

Research output: Contribution to journalArticle

Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletions

Moraes, C. T., Sciacco, M., Ricci, E., Tengan, C. H., Hao, H., Bonilla, E., Schon, E. A. & DiMauro, S., 1995, In : Muscle and Nerve. 18, SUPPL. 3

Research output: Contribution to journalArticle

1996

[43] Cytochemistry and immunocytochemistry of mitochondria in tissue sections

Sciacco, M. & Bonilla, E., 1996, In : Methods in Enzymology. 264, p. 509-517 9 p.

Research output: Contribution to journalArticle

Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle

Prelle, A., Rigoletto, C., Moggio, M., Sciacco, M., Comi, G. P., Ciscato, P., Fagiolari, G., Rapuzzi, S., Bignotti, V. & Scarlato, G., Sep 1 1996, In : Journal of the Neurological Sciences. 140, 1-2, p. 132-136 5 p.

Research output: Contribution to journalArticle

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients

Santorelli, F. M., Sciacco, M., Tanji, K., Shanske, S., Vu, T. H., Golzi, V., Griggs, R. C., Mendell, J. R., Hays, A. P., Bertorini, T. E., Pestronk, A., Bonilla, E. & DiMauro, S., Jun 1996, In : Annals of Neurology. 39, 6, p. 789-795 7 p.

Research output: Contribution to journalArticle

1998

A novel mitochondrial tRNA(Ile) point mutation in chronic progressive external ophthalmoplegia [5]

Franceschina, L., Salani, S., Bordoni, A., Sciacco, M., Napoli, L., Comi, G. P., Prelle, A., Fortunato, F., Hadjigeorgiou, G. M., Farina, E., Bresolin, N., D'Angelo, M. G. & Scarlato, G., 1998, In : Journal of Neurology. 245, 11, p. 755-758 4 p.

Research output: Contribution to journalArticle

Clinical manifestations of mitochondrial DNA depletion

Vu, T. H., Sciacco, M., Tanji, K., Nichter, C., Bonilla, E., Chatkupt, S., Maertens, P., Shanske, S., Mendell, J., Koenigsberger, M. R., Sharer, L., Schon, E. A., DiMauro, S. & DeVivo, D. C., Jun 1998, In : Neurology. 50, 6, p. 1783-1790 8 p.

Research output: Contribution to journalArticle

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease

Comi, G. P., Bordoni, A., Salani, S., Franceschina, L., Sciacco, M., Prelle, A., Fortunato, F., Zeviani, M., Napoli, L., Bresolin, N., Moggio, M., Ausenda, C. D., Taanman, J. W. & Scarlato, G., Jan 1998, In : Annals of Neurology. 43, 1, p. 110-116 7 p.

Research output: Contribution to journalArticle

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome

Papadimitriou, A., Comi, G. P., Hadjigeorgiou, G. M., Bordoni, A., Sciacco, M., Napoli, L., Prelle, A., Moggio, M., Fagiolari, G., Bresolin, N., Salani, S., Anastasopoulos, I., Giassakis, G., Divari, R. & Scarlato, G., Oct 1998, In : Neurology. 51, 4, p. 1086-1092 7 p.

Research output: Contribution to journalArticle

Sarcoglycan deficiency in a large Italian population of myopathic patients

Prelle, A., Comi, G. P., Tancredi, L., Rigoletto, C., Ciscato, P., Fortunato, F., Nesti, S., Sciacco, M., Robotti, M., Bazzi, P., Felisari, G., Moggio, M. & Scarlato, G., Nov 1998, In : Acta Neuropathologica. 96, 5, p. 509-514 6 p.

Research output: Contribution to journalArticle

Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reaction

Sciacco, M., Gasparo-Rippa, P., Vu, T. H., Tanji, K., Shanske, S., Mendell, J. R., Schon, E. A., DiMauro, S. & Bonilla, E., 1998, In : Muscle and Nerve. 21, 11, p. 1374-1381 8 p.

Research output: Contribution to journalArticle

1999

Critically ill patients: Immunological evidence of inflammation in muscle biopsy

Bazzi, P., Moggio, M., Prelle, A., Sciacco, M., Messina, S., Barbieri, S., Tonin, P., Tomelleri, G., Battistel, A., Adobbati, L., Checcarelli, N., Veschi, G. & Scarlato, G., Jan 1999, In : Clinical Neuropathology. 18, 1, p. 23-30 8 p.

Research output: Contribution to journalArticle

2000

A sporadic, atypical case of desminopathy: Morphological and immunological characterization

Prelle, A., Sciacco, M., Comi, G. P., Messina, S., Carpo, M., Ciscato, P., Nobile Orazio, E., Fortunato, F., Mora, G., Bignotti, V., Fagiolari, G., Moggio, M. & Scarlato, G., Jul 2000, In : Clinical Neuropathology. 19, 4, p. 208-212 5 p.

Research output: Contribution to journalArticle

Severe polyneuropathy in a patient with Churg-Strauss syndrome

Bazzi, P., Tancredi, L., Scarpini, E., Messina, S., Sciacco, M., Livraghi, S., Vanoli, M., Prelle, A., Scarlato, G. & Moggio, M., Jun 2000, In : Journal of the Peripheral Nervous System. 5, 2, p. 106-110 5 p.

Research output: Contribution to journalArticle

2001

A novel missense adenine nucleotide translocator-1 gene mutation in a greek adPEO family

Napoli, L., Bordoni, A., Zeviani, M., Hadjigeorgiou, G. M., Sciacco, M., Tiranti, V., Terentiou, A., Moggio, M., Papadimitriou, A., Scarlato, G. & Comi, G. P., Dec 26 2001, In : Neurology. 57, 12, p. 2295-2298 4 p.

Research output: Contribution to journalArticle

Lack of apoptosis in mitochondrial encephalomyopathies

Sciacco, M., Fagiolari, G., Lamperti, C., Messina, S., Bazzi, P., Napoli, L., Chiveri, L., Prelle, A., Comi, G. P., Bresolin, N., Scarlato, G. & Moggio, M., Apr 24 2001, In : Neurology. 56, 8, p. 1070-1074 5 p.

Research output: Contribution to journalArticle

Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation.

Sciacco, M., Prelle, A., Comi, G. P., Napoli, L., Battistel, A., Bresolin, N., Tancredi, L., Lamperti, C., Bordoni, A., Fagiolari, G., Ciscato, P., Chiveri, L., Perini, M. P., Fortunato, F., Adobbati, L., Messina, S., Toscano, A., Martinelli-Boneschi, F., Papadimitriou, A., Scarlato, G. & 1 others, Moggio, M., Sep 2001, In : Journal of Neurology. 248, 9, p. 778-788 11 p.

Research output: Contribution to journalArticle

Retrospective study of a large population of patients affected with mitochondrial disorders: Clinical, morphological and molecular genetic evaluation

Sciacco, M., Prelle, A., Comi, G. P., Napoli, L., Battistel, A., Bresolin, N., Tancredi, L., Lamperti, C., Bordoni, A., Fagiolari, G., Ciscato, P., Chiveri, L., Perini, M. P., Fortunato, F., Adobbati, L., Messina, S., Toscano, A., Martinelli-Boneschi, F., Papadimitriou, A., Scarlato, G. & 1 others, Moggio, M., 2001, In : Journal of Neural Transmission. 108, 8-9, p. 778-788 11 p.

Research output: Contribution to journalArticle

2002

A collection of 33 novel human mtDNA homoplasmic variants.

Crimi, M., Sciacco, M., Galbiati, S., Bordoni, A., Malferrari, G., Del Bo, R., Biunno, I., Bresolin, N. & Comi, G. P., Nov 2002, In : Human Mutation. 20, 5, p. 409 1 p.

Research output: Contribution to journalArticle

Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients

Del Bo, R., Bordoni, A., Boneschi, F. M., Crimi, M., Sciacco, M., Bresolin, N., Scarlato, G. & Comi, G. P., Oct 15 2002, In : Journal of the Neurological Sciences. 202, 1-2, p. 85-91 7 p.

Research output: Contribution to journalArticle

Lack of apoptosis in patients with progressive external ophthalmoplegia and mutated adenine nucleotide translocator-1 gene

Fagiolari, G., Sciacco, M., Chiveri, L., Lamperti, C., Comi, G. P., Scarlato, G., Moggio, M. & Prelle, A., 2002, In : Muscle and Nerve. 26, 2, p. 265-269 5 p.

Research output: Contribution to journalArticle

Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levels

Prelle, A., Tancredi, L., Sciacco, M., Chiveri, L., Comi, G. P., Battistel, A., Bazzi, P., Boneschi, F. M., Bagnardi, V., Ciscato, P., Bordoni, A., Fortunato, F., Strazzer, S., Bresolin, N., Scarlato, G. & Moggio, M., 2002, In : Journal of Neurology. 249, 3, p. 305-311 7 p.

Research output: Contribution to journalArticle

Women with pregnancy-related polymyositis and high serum CK levels in the newborn

Messina, S., Fagiolari, G., Lamperti, C., Cavaletti, G., Prelle, A., Scarlato, G., Bresolin, M., Moggio, M. & Sciacco, M., Feb 12 2002, In : Neurology. 58, 3, p. 482-484 3 p.

Research output: Contribution to journalArticle

2003

A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome

Crimi, M., Galbiati, S., Moroni, I., Bordoni, A., Perini, M. P., Lamantea, E., Sciacco, M., Zeviani, M., Biunno, I., Moggio, M., Scarlato, G. & Comi, G. P., Jun 10 2003, In : Neurology. 60, 11, p. 1857-1861 5 p.

Research output: Contribution to journalArticle

A mitochondrial tRNAHis gene mutation causing pigmentary retinopathy and neurosensorial deafness

Crimi, M., Galbiati, S., Perini, M. P., Bordoni, A., Malferrari, G., Sciacco, M., Biunno, I., Strazzer, S., Moggio, M., Bresolin, N. & Comi, G. P., Apr 8 2003, In : Neurology. 60, 7, p. 1200-1203 4 p.

Research output: Contribution to journalArticle

Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency

Prelle, A., Sciacco, M., Tancredi, L., Fagiolari, G., Comi, G. P., Ciscato, P., Serafini, M., Fortunato, F., Zecca, C., Gallanti, A., Chiveri, L., Bresolin, N., Scarlato, G. & Moggio, M., Jun 1 2003, In : Acta Neuropathologica. 105, 6, p. 537-542 6 p.

Research output: Contribution to journalArticle

Familial mtDNA T8993C transition causing both the NARP and the MILS phenotype in the same generation: A morphological, genetic and spectroscopic study [4]

Sciacco, M., Prelle, A., D'Adda, E., Lamperti, C., Bordoni, A., Rango, M., Crimi, M., Comi, G. P., Bresolin, N. & Moggio, M., Dec 2003, In : Journal of Neurology. 250, 12, p. 1498-1500 3 p.

Research output: Contribution to journalArticle

High mutational burden in the mtDNA control region from aged muscles: A single-fiber study

Del Bo, R., Crimi, M., Sciacco, M., Malferrari, G., Bordoni, A., Napoli, L., Prelle, A., Biunno, I., Moggio, M., Bresolin, N., Scarlato, G. & Comi, G. P., Oct 2003, In : Neurobiology of Aging. 24, 6, p. 829-838 10 p.

Research output: Contribution to journalArticle

Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion

Crimi, M., Del Bo, R., Galbiati, S., Sciacco, M., Bordoni, A., Bresolin, N. & Comi, G. P., Nov 2003, In : European Journal of Human Genetics. 11, 11, p. 896-898 3 p.

Research output: Contribution to journalArticle

Remarkable infidelity of polymerase γA associated with mutations in POLG1 exonuclease domain

Del Bo, R., Bordoni, A., Sciacco, M., Di Fonzo, A., Galbiati, S., Crimi, M., Bresolin, N. & Comi, G. P., Oct 14 2003, In : Neurology. 61, 7, p. 903-908 6 p.

Research output: Contribution to journalArticle

Schizophreniform disorder with cerebrospinal fluid PCR positivity for herpes simplex virus type 1

Chiveri, L., Sciacco, M. & Prelle, A., 2003, In : European Neurology. 50, 3, p. 182-183 2 p.

Research output: Contribution to journalArticle

2004

Mitochondrial-DNA nucleotides G4298A and T10010C as pathogenic mutations: The confirmation in two new cases

Crimi, M., Galbiati, S., Sciacco, M., Bordoni, A., Natali, M. G., Raimondi, M., Bresolin, N. & Comi, G. P., Apr 2004, In : Mitochondrion. 3, 5, p. 279-283 5 p.

Research output: Contribution to journalArticle

2005

A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy

Sciacco, M., Prelle, A., Fagiolari, G., Bordoni, A., Crimi, M., Di Fonzo, A., Ciscato, P., Lamperti, C., D'Adda, E., Jann, S., Bresolin, N., Comi, G. P. & Moggio, M., Dec 15 2005, In : Journal of the Neurological Sciences. 239, 1, p. 21-24 4 p.

Research output: Contribution to journalArticle

Muscle coenzyme Q10 level in statin-related myopathy

Lamperti, C., Naini, A. B., Lucchini, V., Prelle, A., Bresolin, N., Moggio, M., Sciacco, M., Kaufmann, P. & DiMauro, S., Nov 2005, In : Archives of Neurology. 62, 11, p. 1709-1712 4 p.

Research output: Contribution to journalArticle

2006

Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjects

D'Adda, E., Sciacco, M., Fruguglietti, M. E., Crugnola, V., Lucchini, V., Martinelli-Boneschi, F., Zecca, C., Lamperti, C., Comi, G. P., Bresolin, N., Moggio, M. & Prelle, A., Nov 2006, In : Journal of Neurology. 253, 11, p. 1399-1403 5 p.

Research output: Contribution to journalArticle

New mutations in TK2 gene associated with mitochondrial DNA depletion

Galbiati, S., Bordoni, A., Papadimitriou, D., Toscano, A., Rodolico, C., Katsarou, E., Sciacco, M., Garufi, A., Prelle, A., Aguennouz, MH., Bonsignore, M., Crimi, M., Martinuzzi, A., Bresolin, N., Papadimitriou, A. & Comi, G. P., Mar 2006, In : Pediatric Neurology. 34, 3, p. 177-185 9 p.

Research output: Contribution to journalArticle

2009

Aphasic and visual aura with increased vasogenic leakage: An atypical migrainosus status

Lanfranconi, S., Corti, S., Bersano, A., Costa, A., Prelle, A., Sciacco, M., Bresolin, N. & Ghione, I., Oct 15 2009, In : Journal of the Neurological Sciences. 285, 1-2, p. 227-229 3 p.

Research output: Contribution to journalArticle

Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanoma

Fruguglietti, M. E., Napoli, L., Sciacco, M., Ripolone, M., Serafini, M., Grimoldi, N., Bresolin, N., Moggio, M. & Prelle, A., 2009, In : Clinical Neuropathology. 28, 2, p. 125-128 4 p.

Research output: Contribution to journalArticle