• 1466 Citations
  • 19 h-Index
19952019
If you made any changes in Pure these will be visible here soon.

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

  • 7 Similar Profiles
Mutation Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Periventricular Nodular Heterotopia Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Epilepsy Medicine & Life Sciences
Genes Medicine & Life Sciences
Autistic Disorder Medicine & Life Sciences
Neuronal Ceroid-Lipofuscinoses Medicine & Life Sciences

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

Research Output 1995 2019

  • 1466 Citations
  • 19 h-Index
  • 58 Article
  • 1 Review article
1 Citation (Scopus)

Imaging in gynecological disease (15): clinical and ultrasound characteristics of uterine sarcoma

Ludovisi, M., Moro, F., Pasciuto, T., Di Noi, S., Giunchi, S., Savelli, L., Pascual, M. A., Sladkevicius, P., Alcazar, J. L., Franchi, D., Mancari, R., Moruzzi, M. C., Jurkovic, D., Chiappa, V., Guerriero, S., Exacoustos, C., Epstein, E., Frühauf, F., Fischerova, D., Fruscio, R. & 5 others, Ciccarone, F., Zannoni, G. F., Scambia, G., Valentin, L. & Testa, A. C., Jan 1 2019, (Accepted/In press) In : Ultrasound in Obstetrics and Gynecology.

Research output: Contribution to journalArticle

Sarcoma
Endometrial Stromal Sarcoma
Leiomyosarcoma
Neoplasms
Uterine Hemorrhage

SCN11A variant as possible pain generator in sensory axonal neuropathy

Ginanneschi, F., Rubegni, A., Moro, F., Volpi, N., Santorelli, F. M. & Rossi, A., Jan 1 2019, (Accepted/In press) In : Neurological Sciences.

Research output: Contribution to journalArticle

Autophagic vacuolar myopathy caused by a CLN3 mutation. A case report

Moro, F., Rubegni, A., Pochiero, F., Mero, S., Procopio, E., Baldacci, J., Donati, M. A. & Santorelli, F. M., Jan 1 2018, (Accepted/In press) In : Neuromuscular Disorders.

Research output: Contribution to journalArticle

Mitochondrial Encephalomyopathies
Muscles
Mutation
Muscle Weakness
Cardiomegaly
Genetic Association Studies
Cross-Sectional Studies
Dystroglycans
Mutation
Congenital Myasthenic Syndromes

Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study

Astrea, G., Romano, A., Angelini, C., Antozzi, C. G., Barresi, R., Battini, R., Battisti, C., Bertini, E., Bruno, C., Cassandrini, D., Fanin, M., Fattori, F., Fiorillo, C., Guerrini, R., Maggi, L., Mercuri, E., Morani, F., Mora, M., Moro, F., Pezzini, I. & 16 others, Picillo, E., Pinelli, M., Politano, L., Rubegni, A., Sanseverino, W., Savarese, M., Striano, P., Torella, A., Trevisan, C. P., Trovato, R., Zaraieva, I., Muntoni, F., Nigro, V., D'Amico, A., Santorelli, F. M. & Network, I. CMD., 2018, In : Orphanet Journal of Rare Diseases. 13, 1

Research output: Contribution to journalArticle