• 639 Citations
  • 15 h-Index
20062019
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Fingerprint Dive into the research topics where Giovanni Morana is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 7 Similar Profiles
Pediatrics Medicine & Life Sciences
Magnetic Resonance Imaging Medicine & Life Sciences
Neuroimaging Medicine & Life Sciences
Neoplasms Medicine & Life Sciences
Dihydroxyphenylalanine Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences
Brain Medicine & Life Sciences
Glioma Medicine & Life Sciences

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Research Output 2006 2019

  • 639 Citations
  • 15 h-Index
  • 84 Article
  • 10 Chapter
  • 3 Review article
  • 1 Letter

Advanced MR imaging and 18F-DOPA PET characteristics of H3K27M-mutant and wild-type pediatric diffuse midline gliomas

Piccardo, A., Tortora, D., Mascelli, S., Severino, M., Piatelli, G., Consales, A., Pescetto, M., Biassoni, V., Schiavello, E., Massollo, M., Verrico, A., Milanaccio, C., Garrè, M. L., Rossi, A. & Morana, G., Jul 1 2019, In : European Journal of Nuclear Medicine and Molecular Imaging. 46, 8, p. 1685-1694 10 p.

Research output: Contribution to journalArticle

Dihydroxyphenylalanine
Glioma
Pediatrics
Cerebrovascular Circulation
Choline
Sturge-Weber Syndrome
Cavernous Sinus
Port-Wine Stain
Cerebral Veins
Vascular Malformations

Epileptic Encephalopathy, Myoclonus-Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene

Giacomini, T., Vari, M. S., Janis, S., Prato, G., Pisciotta, L., Rocchi, A., Michelucci, A., Di Rocco, M., Gandullia, P., Mattioli, G., Sacco, O., Morana, G. & Mancardi, M. M., Oct 1 2019, In : Neuropediatrics. 50, 5, p. 327-331 5 p.

Research output: Contribution to journalArticle

Brain Diseases
Siblings
Mutation
Genes
Movement Disorders

A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype

Iapadre, G., Morana, G., Vari, M. S., Pinto, F., Lanteri, P., Tessa, A., Santorelli, F. M., Striano, P. & Verrotti, A., May 2018, In : European Journal of Paediatric Neurology. 22, 3, p. 563-567 5 p.

Research output: Contribution to journalArticle

Phenotype
Mutation
Tooth
Polyneuropathies
Genetic Testing