• 27 Citations
  • 4 h-Index
20172018
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Fingerprint Dive into the research topics where Roberta Taurisano is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 3 Similar Profiles
Glycogen Storage Disease Type II Medicine & Life Sciences
Enzyme Replacement Therapy Medicine & Life Sciences
N-acetylglucosamine-6-sulfatase Medicine & Life Sciences
Carbamoyl-Phosphate Synthase I Deficiency Disease Medicine & Life Sciences
Inborn Errors Metabolism Medicine & Life Sciences
Type A Niemann-Pick Disease Medicine & Life Sciences
Mucopolysaccharidosis IV Medicine & Life Sciences
Biomarkers Medicine & Life Sciences

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Research Output 2017 2018

  • 27 Citations
  • 4 h-Index
  • 11 Article

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

11 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
Neuroimaging

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., 2018, In : Orphanet Journal of Rare Diseases. 13, 1

Research output: Contribution to journalArticle

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, 12 p., 32.

Research output: Contribution to journalArticle

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

microRNAs as biomarkers in Pompe disease

Tarallo, A., Carissimo, A., Gatto, F., Nusco, E., Toscano, A., Musumeci, O., Coletta, M., Karali, M., Acampora, E., Damiano, C., Minopoli, N., Fecarotta, S., Della Casa, R., Mongini, T., Vercelli, L., Santoro, L., Ruggiero, L., Deodato, F., Taurisano, R., Bembi, B. & 5 others, Dardis, A., Banfi, S., Pijnappel, W. W. P., van der Ploeg, A. T. & Parenti, G., Jul 12 2018, In : Genetics in Medicine. 10 p.

Research output: Contribution to journalArticle

Glycogen Storage Disease Type II
MicroRNAs
Biomarkers
Enzyme Replacement Therapy
Muscular Atrophy