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

  • 13 Similar Profiles
Neurofibromatosis 1 Medicine & Life Sciences
inherited metabolic diseases Agriculture & Biology
Inborn Errors Metabolism Medicine & Life Sciences
Rubinstein-Taybi Syndrome Medicine & Life Sciences
Enzyme Replacement Therapy Medicine & Life Sciences
Glycogen Storage Disease Type II Medicine & Life Sciences
Vaccination Medicine & Life Sciences
Vaccines Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1996 2019

  • 657 Citations
  • 13 h-Index
  • 39 Article
  • 2 Review article
Open Access
Pseudotumor Cerebri
Mycoplasma pneumoniae
Levofloxacin
Infection
Headache

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
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

2 Citations (Scopus)

Progressive bone impairment with age and pubertal development in neurofibromatosis type I

Rodari, G., Scuvera, G., Ulivieri, F. M., Profka, E., Menni, F., Saletti, V., Esposito, S., Bergamaschi, S., Ferrante, E., Eller-Vainicher, C., Esposito, S., Arosio, M. & Giavoli, C., Dec 1 2018, In : Archives of Osteoporosis. 13, 1, 93.

Research output: Contribution to journalArticle

Neurofibromatosis 1
Bone and Bones
Bone Density
Spine
Photon Absorptiometry