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

  • 7 Similar Profiles
Opsoclonus-Myoclonus Syndrome Medicine & Life Sciences
Mutation Medicine & Life Sciences
Neuroblastoma Medicine & Life Sciences
Myelin-Oligodendrocyte Glycoprotein Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences
Pediatrics Medicine & Life Sciences
Periventricular Leukomalacia Medicine & Life Sciences
Optic Neuritis Medicine & Life Sciences

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Research Output 2006 2020

Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients

Giacomini, T., Foiadelli, T., Annovazzi, P., Nosadini, M., Gastaldi, M., Franciotta, D., Panarese, C., Capris, P., Camicione, P., Lanteri, P., De Grandis, E., Prato, G., Cordani, R., Nobili, L., Morana, G., Rossi, A., Pistorio, A., Cellerino, M., Uccelli, A., Sartori, S. & 2 others, Savasta, S. & Mancardi, M. M., Apr 2020, In : Multiple Sclerosis and Related Disorders. 39, 101917.

Research output: Contribution to journalArticle

Myelin-Oligodendrocyte Glycoprotein
Optic Neuritis
Pediatrics
Antibodies
Nerve Fibers

PANDAS and PANS: Clinical, Neuropsychological, and Biological Characterization of a Monocentric Series of Patients and Proposal for a Diagnostic Protocol

Gamucci, A., Uccella, S., Sciarretta, L., D'Apruzzo, M., Calevo, M. G., Mancardi, M. M., Veneselli, E. & De Grandis, E., May 2019, In : Journal of Child and Adolescent Psychopharmacology. 29, 4, p. 305-312 8 p.

Research output: Contribution to journalArticle

Pediatrics
Chorea
Tic Disorders
Behavioral Symptoms
Aptitude

Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients

Giacomini, T., Foiadelli, T., Annovazzi, P., Nosadini, M., Gastaldi, M., Franciotta, D., Panarese, C., Capris, P., Camicione, P., Lanteri, P., De Grandis, E., Prato, G., Cordani, R., Nobili, L., Morana, G., Rossi, A., Pistorio, A., Cellerino, M., Uccelli, A., Sartori, S. & 2 others, Savasta, S. & Mancardi, M. M., Dec 24 2019, In : Multiple Sclerosis and Related Disorders. 39, p. 101917

Research output: Contribution to journalArticle

Myelin-Oligodendrocyte Glycoprotein
Optic Neuritis
Pediatrics
Antibodies
Nerve Fibers

A novel pathogenic MYH3 mutation in a child with Sheldon–Hall syndrome and vertebral fusions

Scala, M., Accogli, A., De Grandis, E., Allegri, A., Bagowski, C. P., Shoukier, M., Maghnie, M. & Capra, V., Mar 1 2018, In : American Journal of Medical Genetics, Part A. 176, 3, p. 663-667 5 p.

Research output: Contribution to journalArticle

Mutation
Arthrogryposis
Muscle Development
Bone Development
Contracture