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

  • 37 Similar Profiles
Epilepsy Medicine & Life Sciences
Seizures Medicine & Life Sciences
Encephalitis Medicine & Life Sciences
Myoclonic Epilepsy Medicine & Life Sciences
Electroencephalography Medicine & Life Sciences
Mutation Medicine & Life Sciences
Partial Epilepsy Medicine & Life Sciences
Infantile Spasms Medicine & Life Sciences

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Research Output 1988 2019

Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study

Di Marco, R., Hallemans, A., Bellon, G., Ragona, F., Piazza, E., Granata, T., Ceulemans, B., Schoonjans, A-S., Van de Walle, P., Darra, F., Dalla Bernardina, B., Vecchi, M., Sawacha, Z., Scarpa, B., Masiero, S., Benedetti, M. G. & Del Felice, A., Sep 21 2019, In : European Journal of Paediatric Neurology.

Research output: Contribution to journalArticle

Myoclonic Epilepsy
Gait
Knee
Articular Range of Motion
Biomechanical Phenomena

Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation

Canafoglia, L., Castellotti, B., Ragona, F., Freri, E., Granata, T., Chiapparini, L., Gellera, C., Scaioli, V., Franceschetti, S. & DiFrancesco, J. C., Feb 1 2019, In : Seizure. 65, p. 106-108 3 p.

Research output: Contribution to journalArticle

Relapse risk factors in anti-N-methyl-D-aspartate receptor encephalitis

Italian Working Group on Paediatric Anti-N-methyl-D-aspartate Receptor Encephalitis, Jun 7 2019, In : Developmental Medicine and Child Neurology.

Research output: Contribution to journalArticle

Anti-N-Methyl-D-Aspartate Receptor Encephalitis
Recurrence
Survival Analysis
Age of Onset
Intensive Care Units
5 Citations (Scopus)

A causality algorithm to guide diagnosis and treatment of catatonia due to autoimmune conditions in children and adolescents

Ferrafiat, V., Raffin, M., Freri, E., Granata, T., Nardocci, N., Zibordi, F., Bodeau, N., Benarous, X., Olliac, B., Riquin, E., Xavier, J., Viaux, S., Haroche, J., Amoura, Z., Gerardin, P., Cohen, D. & Consoli, A., Oct 1 2018, In : Schizophrenia Research. 200, p. 68-76 9 p.

Research output: Contribution to journalArticle

Catatonia
Causality
Therapeutics
ROC Curve
Pediatrics
3 Citations (Scopus)

A loss-of-function HCN4 mutation associated with familial benign myoclonic epilepsy in infancy causes increased neuronal excitability

Campostrini, G., Difrancesco, J. C., Castellotti, B., Milanesi, R., Gnecchi-Ruscone, T., Bonzanni, M., Bucchi, A., Baruscotti, M., Ferrarese, C., Franceschetti, S., Canafoglia, L., Ragona, F., Freri, E., Labate, A., Gambardella, A., Costa, C., Gellera, C., Granata, T., Barbuti, A. & Difrancesco, D., Jan 1 2018, In : Frontiers in Molecular Neuroscience. 11, 269.

Research output: Contribution to journalArticle

Myoclonic Epilepsy
Epilepsy
Mutation
Neurons
Brain