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

  • 19 Similar Profiles
Mitochondrial Diseases Medicine & Life Sciences
Mutation Medicine & Life Sciences
Glycogen Storage Disease Type II Medicine & Life Sciences
Enzyme Replacement Therapy Medicine & Life Sciences
Hereditary Spastic Paraplegia Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Nemaline Myopathies Medicine & Life Sciences
Mitochondrial DNA Medicine & Life Sciences

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Research Output 2018 2019

  • 22 Citations
  • 3 h-Index
  • 17 Article
  • 3 Letter
  • 1 Review article

Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group

Filosto, M., Cotti Piccinelli, S., Ravaglia, S., Servidei, S., Moggio, M., Musumeci, O., Donati, M. A., Pegoraro, E., Di Muzio, A., Maggi, L., Tonin, P., Marrosu, G., Sancricca, C., Lerario, A., Sacchini, M., Semplicini, C., Bozzoni, V., Telese, R., Bonanno, S., Piras, R. & 10 others, Maioli, M. A., Ricci, G., Vercelli, L., Galvagni, A., Gallo Cassarino, S., Caria, F., Mongini, T., Siciliano, G., Padovani, A. & Toscano, A., May 2019, In : Advances in Therapy. 36, 5, p. 1177-1189 13 p.

Research output: Contribution to journalArticle

Glycogen Storage Disease Type II
Enzyme Replacement Therapy
Antibodies
Late Onset Disorders
Vital Capacity
1 Citation (Scopus)

Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group

Filosto, M., Cotti Piccinelli, S., Ravaglia, S., Servidei, S., Moggio, M., Musumeci, O., Donati, M. A., Pegoraro, E., Di Muzio, A., Maggi, L., Tonin, P., Marrosu, G., Sancricca, C., Lerario, A., Sacchini, M., Semplicini, C., Bozzoni, V., Telese, R., Bonanno, S., Piras, R. & 10 others, Maioli, M. A., Ricci, G., Vercelli, L., Galvagni, A., Gallo Cassarino, S., Caria, F., Mongini, T., Siciliano, G., Padovani, A. & Toscano, A., Jan 1 2019, In : Advances in Therapy. 36, 5, p. 1177-1189

Research output: Contribution to journalArticle

Glycogen Storage Disease Type II
Enzyme Replacement Therapy
Antibodies
Late Onset Disorders
Vital Capacity
Hereditary Spastic Paraplegia
Mutation
Brain
Magnetic Resonance Imaging
Phenotype
Hereditary Spastic Paraplegia
Mutation
Brain
Magnetic Resonance Imaging
Phenotype
1 Citation (Scopus)

Limb-Girdle Muscular Dystrophies (LGMDs): The clinical application of NGS analysis, a family case report

Strafella, C., Campoli, G., Galota, R. M., Caputo, V., Pagliaroli, G., Carboni, S., Zampatti, S., Peconi, C., Mela, J., Sancricca, C., Primiano, G., Minozzi, G., Servidei, S., Cascella, R. & Giardina, E., Jan 1 2019, In : Frontiers in Neurology. 10, JUN, 619.

Research output: Contribution to journalArticle

Open Access
Limb-Girdle Muscular Dystrophies
Cardiomyopathies
Mothers
Inheritance Patterns
Mutation