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Thea Giacomini

Showing results (1-10 of 50) with videos related to

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Cytogenetic and Genome Research|December 4, 2018
Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number VariationsElisa Tassano, Sara Uccella, Thea Giacomini, et al.
Cytogenetic and Genome Research|June 13, 2017
Characterization of the Phenotype Associated with Microduplication Reciprocal to NF1 Microdeletion SyndromeElisa Tassano, Thea Giacomini, Mariasavina Severino, et al.
Cytogenetic and Genome Research|August 8, 2018
Intragenic Microdeletion of ULK4 and Partial Microduplication of BRWD3 in Siblings with Neuropsychiatric Features and ObesityElisa Tassano, Sara Uccella, Thea Giacomini, et al.
European Journal of Medical Genetics|March 27, 2020
1p31.1 microdeletion including only NEGR1 gene in two patientsElisa Tassano, Sara Uccella, Thea Giacomini, et al.
Neuropediatrics|April 10, 2018
Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral PhenotypeLivia Pisciotta, Valeria Capra, Andrea Accogli, et al.
Neuroradiology|May 17, 2020
Spatial coefficient of variation applied to arterial spin labeling MRI may contribute to predict surgical revascularization outcomes in pediatric moyamoya vasculopathyDomenico Tortora, Camilla Scavetta, Giacomo Rebella, et al.
Journal of Genetics|March 12, 2021
Expanding the phenotype associated with interstitial 6p25.1p24.3 microdeletion: a new case and review of the literatureElisa Tassano, Sara Uccella, Mariasavina Severino, et al.
Neuroradiology|June 6, 2020
Correction to: Spatial coefficient of variation applied to arterial spin labeling MRI may contribute to predict surgical revascularization outcomes in pediatric moyamoya vasculopathyDomenico Tortora, Camilla Scavetta, Giacomo Rebella, et al.
BMC Neurology|August 29, 2025
Refractory "status dyskineticus" in a child with post-herpes simplex virus 1 N-methyl-D-aspartate receptor encephalitis: a case reportAlessandro Santagostino Barbone, Elisa De Grandis, Thea Giacomini, et al.
European Journal of Medical Genetics|March 5, 2018
3q29 microduplication syndrome: Description of two new cases and delineation of the minimal critical regionElisa Tassano, Sara Uccella, Thea Giacomini, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Cytogenetic and Genome Research|December 4, 2018
Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number VariationsElisa Tassano, Sara Uccella, Thea Giacomini, et al.
Cytogenetic and Genome Research|June 13, 2017
Characterization of the Phenotype Associated with Microduplication Reciprocal to NF1 Microdeletion SyndromeElisa Tassano, Thea Giacomini, Mariasavina Severino, et al.
Cytogenetic and Genome Research|August 8, 2018
Intragenic Microdeletion of ULK4 and Partial Microduplication of BRWD3 in Siblings with Neuropsychiatric Features and ObesityElisa Tassano, Sara Uccella, Thea Giacomini, et al.
European Journal of Medical Genetics|March 27, 2020
1p31.1 microdeletion including only NEGR1 gene in two patientsElisa Tassano, Sara Uccella, Thea Giacomini, et al.
Neuropediatrics|April 10, 2018
Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral PhenotypeLivia Pisciotta, Valeria Capra, Andrea Accogli, et al.
Neuroradiology|May 17, 2020
Spatial coefficient of variation applied to arterial spin labeling MRI may contribute to predict surgical revascularization outcomes in pediatric moyamoya vasculopathyDomenico Tortora, Camilla Scavetta, Giacomo Rebella, et al.
Journal of Genetics|March 12, 2021
Expanding the phenotype associated with interstitial 6p25.1p24.3 microdeletion: a new case and review of the literatureElisa Tassano, Sara Uccella, Mariasavina Severino, et al.
Neuroradiology|June 6, 2020
Correction to: Spatial coefficient of variation applied to arterial spin labeling MRI may contribute to predict surgical revascularization outcomes in pediatric moyamoya vasculopathyDomenico Tortora, Camilla Scavetta, Giacomo Rebella, et al.
BMC Neurology|August 29, 2025
Refractory "status dyskineticus" in a child with post-herpes simplex virus 1 N-methyl-D-aspartate receptor encephalitis: a case reportAlessandro Santagostino Barbone, Elisa De Grandis, Thea Giacomini, et al.
European Journal of Medical Genetics|March 5, 2018
3q29 microduplication syndrome: Description of two new cases and delineation of the minimal critical regionElisa Tassano, Sara Uccella, Thea Giacomini, et al.
Pageof 5