• 1146 Citations
  • 18 h-Index
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Fingerprint Dive into the research topics where Federica Deodato is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 10 Similar Profiles
Glycogen Storage Disease Type II Medicine & Life Sciences
Enzyme Replacement Therapy Medicine & Life Sciences
Mutation Medicine & Life Sciences
Vitamin B 12 Medicine & Life Sciences
Type C Niemann-Pick Disease Medicine & Life Sciences
Mucopolysaccharidosis I Medicine & Life Sciences
Homocystinuria Medicine & Life Sciences
Propionic Acidemia Medicine & Life Sciences

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Research Output 2002 2019

  • 1146 Citations
  • 18 h-Index
  • 44 Article
  • 2 Review article

Pain REduction with bone metastases STereotactic radiotherapy (PREST): A phase III randomized multicentric trial

Cellini, F., Manfrida, S., Deodato, F., Cilla, S., Maranzano, E., Pergolizzi, S., Arcidiacono, F., Di Franco, R., Pastore, F., Muto, M., Borzillo, V., Donati, C. M., Siepe, G., Parisi, S., Salatino, A., D'Agostino, A., Montesi, G., Santacaterina, A., Fusco, V., Santarelli, M. & 6 others, Gambacorta, M. A., Corvò, R., Morganti, A. G., Masiello, V., Muto, P. & Valentini, V., 2019, In : Trials. 20, 1

Research output: Contribution to journalArticle

Mucopolysaccharidosis I
Genetic Therapy
Hematopoietic Stem Cells

Axonal peripheral neuropathy in propionic acidemia: A severe side effect of long-term metronidazole therapy

Diodato, D., Olivieri, G., Pro, S., Maiorani, D., Martinelli, D., Deodato, F., Taurisano, R., Di Capua, M. & Dionisi-Vici, C., Sep 18 2018, In : Neurology. 91, 12, p. 565-567 3 p.

Research output: Contribution to journalArticle

Enzyme replacement therapy: efficacy and limitations

Concolino, D., Deodato, F. & Parini, R., Nov 16 2018, In : Italian Journal of Pediatrics. 44, Suppl 2, p. 120 10 p.

Research output: Contribution to journalReview article

Enzyme Replacement Therapy
Mucopolysaccharidosis II
Mucopolysaccharidosis I
Mucopolysaccharidosis VI
12 Citations (Scopus)

Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy

Parini, R., De Lorenzo, P., Dardis, A., Burlina, A., Cassio, A., Cavarzere, P., Concolino, D., Della Casa, R., Deodato, F., Donati, M. A., Fiumara, A., Gasperini, S., Menni, F., Pagliardini, V., Sacchini, M., Spada, M., Taurisano, R., Valsecchi, M. G., Di Rocco, M. & Bembi, B., Feb 8 2018, In : Orphanet Journal of Rare Diseases. 13, 1, 32.

Research output: Contribution to journalArticle

Glycogen Storage Disease Type II
Enzyme Replacement Therapy
Multicenter Studies
Age of Onset