Istituto "Giannina Gaslini"

Fingerprint Dive into the research topics where Istituto "Giannina Gaslini" is active. These topic labels come from the works of this organisation's members. Together they form a unique fingerprint.

Pediatrics Medicine & Life Sciences
Mutation Medicine & Life Sciences
Neuroblastoma Medicine & Life Sciences
Juvenile Arthritis Medicine & Life Sciences
Natural Killer Cells Medicine & Life Sciences
Therapeutics Medicine & Life Sciences
Genes Medicine & Life Sciences
Neoplasms Medicine & Life Sciences

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Projects 2018 2018

GASLINI - STRATEGIE DIAGNOSTICO-TERAPEUTICHE INNOVATIVE E MALATTIE RARE

Ricerca, U.

1/1/1812/30/18

Project: Other project

GASLINI - SCIENZE PEDIATRICHE, CHIRURGIA E NEONATOLOGIA

Ricerca, U.

1/1/1812/30/18

Project: Other project

GASLINI - PATOLOGIE MUSCOLARI E NEUROLOGICHE

Ricerca, U.

1/1/1812/30/18

Project: Other project

Research Output 1971 2019

Abnormal circadian rhythm in patients with GRIN1-related developmental epileptic encephalopathy

Scala, M., Amadori, E., Fusco, L., Marchese, F., Capra, V., Minetti, C., Vari, M. S. & Striano, P., May 24 2019, In : European Journal of Paediatric Neurology.

Research output: Contribution to journalArticle

Brain Diseases
Circadian Rhythm
Sleep
Crying
Inborn Genetic Diseases

Accuracy and Limitations of the Growth Hormone (GH) Releasing Hormone-Arginine Retesting in Young Adults With Childhood-Onset GH Deficiency

Patti, G., Noli, S., Capalbo, D., Allegri, A. M. E., Napoli, F., Cappa, M., Ubertini, G. M., Gallizia, A., Notarnicola, S., Ibba, A., Crocco, M., Parodi, S., Salerno, M., Loche, S., Garré, M. L., Tornari, E., Maghnie, M. & Di Iorgi, N., 2019, In : Frontiers in Endocrinology. 10, p. 525

Research output: Contribution to journalArticle

Growth Hormone-Releasing Hormone
Growth Hormone
Arginine
Young Adult
Hormones

A clinical diagnostic algorithm for early onset cerebellar ataxia

Brandsma, R., Verschuuren-Bemelmans, C. C., Amrom, D., Barisic, N., Baxter, P., Bertini, E., Blumkin, L., Brankovic-Sreckovic, V., Brouwer, O. F., Bürk, K., Catsman-Berrevoets, C. E., Craiu, D., de Coo, I. F. M., Gburek, J., Kennedy, C., de Koning, T. J., Kremer, H. P. H., Kumar, R., Macaya, A., Micalizzi, A. & 14 others, Mirabelli-Badenier, M., Nemeth, A., Nuovo, S., Poll-The, B., Lerman-Sagie, T., Steinlin, M., Synofzik, M., Tijssen, M. A. J., Vasco, G., Willemsen, M. A. A. P., Zanni, G., Valente, E. M., Boltshauser, E. & Sival, D. A., Aug 10 2019, In : European Journal of Paediatric Neurology.

Research output: Contribution to journalArticle

Spinocerebellar Degenerations
Cerebellar Ataxia
Genetic Testing
Neurology
Differential Diagnosis