Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization
Camille Engel, Michaela Rendek, Jessica Assoumani, Emanuela Argilli et autres
0 citationsEuropean Journal of Human Genetics
Thea Giacomini
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75Publications signalées
1109Citations signalées
3Affiliations récentes
Institutions déclarées
Domaines associés
Epilepsy research and treatmentGenetics and Neurodevelopmental DisordersGenomics and Rare DiseasesMultiple Sclerosis Research StudiesAdvanced MRI Techniques and Applications
Publications récentes
Correction to: Head to head comparison between arterial spin labelling MRI and [18F]FDG-PET in presurgical evaluation of epilepsy in children: the role of voxel-based asymmetry index analysis
Pietro Mattioli, Giulia Nobile, Matteo Cataldi, Luca Bosisio et autres
1 citationNeurological Sciences
Head to head comparison between arterial spin labelling MRI and [18F]FDG-PET in presurgical evaluation of epilepsy in children: the role of voxel-based asymmetry index analysis
Pietro Mattioli, Giulia Nobile, Matteo Cataldi, Luca Bosisio et autres
0 citationsNeurological Sciences
First demyelinating attack in children: A twelve year single center cohort
Alessandro Santagostino Barbone, Thea Giacomini, Silvia Casabona, Elisa De Grandis et autres
1 citationMultiple Sclerosis and Related Disorders
Refractory “status dyskineticus” in a child with post-herpes simplex virus 1 N-methyl-D-aspartate receptor encephalitis: a case report
Alessandro Santagostino Barbone, Elisa De Grandis, Thea Giacomini, Silvia Buratti et autres
1 citationBMC Neurology
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization
Camille Engel, Michaela Rendek, Jessica Assoumani, Emanuela Argilli et autres
4 citationsEuropean Journal of Human Genetics
Multidisciplinary, multicenter consensus for the care of patients affected with Sturge–Weber syndrome
May El Hachem, Andrea Diociaiuti, Angela Galeotti, Francesca Grussu et autres
14 citationsOrphanet Journal of Rare Diseases
Surgical treatment of cavernous malformation-related epilepsy in children: case series, systematic review, and meta-analysis
Luca Bosisio, Erica Cognolato, Giulia Nobile, Maria Margherita Mancardi et autres
5 citationsNeurosurgical Review
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA‐Epilepsy study
Rebecca Kerestes, Andrew Perry, Lucy Vivash, Terence J. O’Brien et autres
24 citationsEpilepsia
Brain and spine malformations and neurodevelopmental disorders in a cohort of children with CAKUT
Silvia Boeri, Monica Bodria, Rosa Maria Ammendola, Thea Giacomini et autres
3 citationsPediatric Nephrology
Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities
Marcello Scala, Kamal Khan, Claire Bénéteau, Rachel Fox et autres
11 citationsGenetics in Medicine
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study
Rebecca Kerestes, Andrew Perry, Lucy Vivash, Terence J. O’Brien et autres
4 citationsbioRxiv (Cold Spring Harbor Laboratory)
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