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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.

  • 47 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

  • 3353 Citations
  • 30 h-Index
  • 95 Article
  • 2 Letter
  • 1 Comment/debate
  • 1 Review article
1 Citation (Scopus)

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
6 Citations (Scopus)

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
1 Citation (Scopus)
Cytochrome-c Oxidase Deficiency
Spinocerebellar Ataxias
Purkinje Cells
Animal Models
Transgenic Mice
7 Citations (Scopus)

Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies

Feichtinger, R. G., Oláhová, M., Kishita, Y., Garone, C., Kremer, L. S., Yagi, M., Uchiumi, T., Jourdain, A. A., Thompson, K., D'Souza, A. R., Kopajtich, R., Alston, C. L., Koch, J., Sperl, W., Mastantuono, E., Strom, T. M., Wortmann, S. B., Meitinger, T., Pierre, G., Chinnery, P. F. & 19 others, Chrzanowska-Lightowlers, Z. M., Lightowlers, R. N., DiMauro, S., Calvo, S. E., Mootha, V. K., Moggio, M., Sciacco, M., Comi, G. P., Ronchi, D., Murayama, K., Ohtake, A., Rebelo-Guiomar, P., Kohda, M., Kang, D., Mayr, J. A., Taylor, R. W., Okazaki, Y., Minczuk, M. & Prokisch, H., 2017, In : American Journal of Human Genetics. 101, 4, p. 525-538

Research output: Contribution to journalArticle

Chronic Progressive External Ophthalmoplegia
Oxidative Phosphorylation
Muscular Diseases
Electron Transport