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Fingerprint Dive into the research topics where Monica Sciacco is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 45 Similar Profiles
Mitochondrial DNA Medicine & Life Sciences
Mutation Medicine & Life Sciences
Muscles Medicine & Life Sciences
Chronic Progressive External Ophthalmoplegia Medicine & Life Sciences
Mitochondrial Diseases Medicine & Life Sciences
Mitochondrial Encephalomyopathies Medicine & Life Sciences
Biopsy Medicine & Life Sciences
Skeletal Muscle Medicine & Life Sciences

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Research Output 1991 2019

Can intestinal pseudo-obstruction drive recurrent stroke-like episodes in late-onset MELAS syndrome? A case report and review of the literature

Gagliardi, D., Mauri, E., Magri, F., Velardo, D., Meneri, M., Abati, E., Brusa, R., Faravelli, I., Piga, D., Ronchi, D., Triulzi, F., Peverelli, L., Sciacco, M., Bresolin, N., Comi, G. P., Corti, S. & Govoni, A., Jan 1 2019, In : Frontiers in Neurology. 10, JAN, 38.

Research output: Contribution to journalArticle

Open Access
MELAS Syndrome
Intestinal Pseudo-Obstruction
Mitochondrial Diseases

Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophy

Galimberti, V., Tironi, R., Lerario, A., Scali, M., Del Bo, R., Rodolico, C., Brizzi, T., Gibertini, S., Maggi, L., Mora, M., Toscano, A., Comi, G. P., Sciacco, M., Moggio, M. & Peverelli, L., Jan 1 2019, (Accepted/In press) In : European Journal of Neurology.

Research output: Contribution to journalArticle

Oculopharyngeal Muscular Dystrophy
Chronic Progressive External Ophthalmoplegia
Inclusion Body Myositis

Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD)

Ripolone, M., Violano, R., Ronchi, D., Mondello, S., Nascimbeni, A., Colombo, I., Fagiolari, G., Bordoni, A., Fortunato, F., Lucchini, V., Simona, S., Filosto, M., Musumeci, O., Tonin, P., Mongini, T., Previtali, S., Morandi, L., Angelini, C., Mora, M., Sandri, M. & 4 others, Sciacco, M., Toscano, A., Comi, G. P. & Moggio, M., 2018, In : Neuropathology and Applied Neurobiology. 44, 5, p. 449-462

Research output: Contribution to journalArticle

Glycogen Storage Disease Type II
Enzyme Replacement Therapy
Skeletal Muscle

Purkinje cell cox deficiency and mtdna depletion in an animal model of spinocerebellar ataxia type 1

Ripolone, M., Lucchini, V., Ronchi, D., Fagiolari, G., Bordoni, A., Fortunato, F., Mondello, S., Bonato, S., Meregalli, M., Torrente, Y., Corti, S., Comi, G. P., Moggio, M. & Sciacco, M., Jan 1 2018, In : Journal of Neuroscience Research. 96, 9, p. 1576-1585 10 p.

Research output: Contribution to journalArticle

Cytochrome-c Oxidase Deficiency
Spinocerebellar Ataxias
Purkinje Cells
Animal Models
Transgenic Mice