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Stefano Sotgiu

Showing results (71-80 of 93) with videos related to

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Clinical Neurophysiology Practice|July 14, 2021
Occurrence of hyperventilation-induced high amplitude rhythmic slowing with altered awareness after successful treatment of typical absence seizures and a network hypothesisSimone Mattozzi, Caterina Cerminara, Maria A Sotgiu, et al.
BMC Genetics|May 19, 2007
Variation of the myelin oligodendrocyte glycoprotein gene is not primarily associated with multiple sclerosis in the Sardinian populationMaria Giovanna Marrosu, Raffaele Murru, Gianna Costa, et al.
Autism Research : Official Journal of the International Society for Autism Research|February 22, 2020
Vitamin D Receptor Polymorphisms Associated with Autism Spectrum DisorderFranca Rosa Guerini, Elisabetta Bolognesi, Matteo Chiappedi, et al.
International Journal of Biomedical Science : IJBS|May 16, 2013
Multiple Sclerosis and HERV-W/MSRV: A Multicentric StudyGiannina Arru, Giuseppe Mameli, Vito Astone, et al.
Brain, Behavior, and Immunity|September 20, 2017
HLA-G coding region polymorphism is skewed in autistic spectrum disordersFranca R Guerini, Elisabetta Bolognesi, Matteo Chiappedi, et al.
Brain, Behavior, and Immunity|February 15, 2019
HLA-G allelic distribution in Sardinian children with Autism spectrum disorders: A replication studyFranca R Guerini, Elisabetta Bolognesi, Stefano Sotgiu, et al.
Journal of Clinical Medicine|November 11, 2022
<sup>1</sup>H-NMR-Based Metabolomics in Autism Spectrum Disorder and Pediatric Acute-Onset Neuropsychiatric SyndromeAntonella Gagliano, Federica Murgia, Agata Maria Capodiferro, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|October 8, 2025
Applying the Supporting Features for MOGAD Diagnosis to Patients With Multiple SclerosisPietro Zara, Giacomo Greco, Francesco Masi, et al.
International Journal of Molecular Sciences|December 29, 2017
Clinical and Neurobehavioral Features of Three Novel Kabuki Syndrome Patients with Mosaic KMT2D Mutations and a Review of LiteratureFrancesca Romana Lepri, Dario Cocciadiferro, Bartolomeo Augello, et al.
Journal of Neurology|June 20, 2008
Analysis of 45 candidate genes for disease modifying activity in multiple sclerosisSreeram V Ramagopalan, Gabriele C Deluca, Katie M Morrison, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
Clinical Neurophysiology Practice|July 14, 2021
Occurrence of hyperventilation-induced high amplitude rhythmic slowing with altered awareness after successful treatment of typical absence seizures and a network hypothesisSimone Mattozzi, Caterina Cerminara, Maria A Sotgiu, et al.
BMC Genetics|May 19, 2007
Variation of the myelin oligodendrocyte glycoprotein gene is not primarily associated with multiple sclerosis in the Sardinian populationMaria Giovanna Marrosu, Raffaele Murru, Gianna Costa, et al.
Autism Research : Official Journal of the International Society for Autism Research|February 22, 2020
Vitamin D Receptor Polymorphisms Associated with Autism Spectrum DisorderFranca Rosa Guerini, Elisabetta Bolognesi, Matteo Chiappedi, et al.
International Journal of Biomedical Science : IJBS|May 16, 2013
Multiple Sclerosis and HERV-W/MSRV: A Multicentric StudyGiannina Arru, Giuseppe Mameli, Vito Astone, et al.
Brain, Behavior, and Immunity|September 20, 2017
HLA-G coding region polymorphism is skewed in autistic spectrum disordersFranca R Guerini, Elisabetta Bolognesi, Matteo Chiappedi, et al.
Brain, Behavior, and Immunity|February 15, 2019
HLA-G allelic distribution in Sardinian children with Autism spectrum disorders: A replication studyFranca R Guerini, Elisabetta Bolognesi, Stefano Sotgiu, et al.
Journal of Clinical Medicine|November 11, 2022
<sup>1</sup>H-NMR-Based Metabolomics in Autism Spectrum Disorder and Pediatric Acute-Onset Neuropsychiatric SyndromeAntonella Gagliano, Federica Murgia, Agata Maria Capodiferro, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|October 8, 2025
Applying the Supporting Features for MOGAD Diagnosis to Patients With Multiple SclerosisPietro Zara, Giacomo Greco, Francesco Masi, et al.
International Journal of Molecular Sciences|December 29, 2017
Clinical and Neurobehavioral Features of Three Novel Kabuki Syndrome Patients with Mosaic KMT2D Mutations and a Review of LiteratureFrancesca Romana Lepri, Dario Cocciadiferro, Bartolomeo Augello, et al.
Journal of Neurology|June 20, 2008
Analysis of 45 candidate genes for disease modifying activity in multiple sclerosisSreeram V Ramagopalan, Gabriele C Deluca, Katie M Morrison, et al.
Pageof 10