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Stefano Sotgiu

Showing results (61-70 of 93) with videos related to

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Journal of Neurology|May 9, 2003
Investigation of a genetic variation of a variable number tandem repeat polymorphism of interleukin-6 gene in patients with multiple sclerosisStephan Schmidt, Andreas Papassotiropoulos, Stefano Sotgiu, et al.
Cytokine|May 20, 2004
High frequency of TNF alleles -238A and -376A in individuals from northern SardiniaSebastian A Wirz, Maria C Morale, Bianca Marchetti, et al.
Microorganisms|January 25, 2025
HERVs Endophenotype in Autism Spectrum Disorder: Human Endogenous Retroviruses, Specific Immunoreactivity, and Disease Association in Different Family MembersMarco Bo, Alessandra Carta, Chiara Cipriani, et al.
Human Immunology|May 16, 2006
A family based linkage analysis of HLA and 5-HTTLPR gene polymorphisms in Sardinian children with autism spectrum disorderFranca R Guerini, Salvatorica Manca, Stefano Sotgiu, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|June 9, 2021
Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspringAlessandra Carta, Ignazio R Zarbo, Chiara Scoppola, et al.
Neuroscience|June 20, 2017
HLA-G∗14bp Insertion and the KIR2DS1-HLAC2 Complex Impact on Behavioral Impairment in Children with Autism Spectrum DisordersFranca R Guerini, Elisabetta Bolognesi, Matteo Chiappedi, et al.
Multiple Sclerosis and Related Disorders|March 10, 2024
Epidemiology of aquaporin-4-IgG-positive NMOSD in SardiniaElia Sechi, Mariangela Puci, Maria Ida Pateri, et al.
BMC Medical Genetics|May 9, 2019
VARS2-linked mitochondrial encephalopathy: two case reports enlarging the clinical phenotypeChiara Begliuomini, Giorgio Magli, Maja Di Rocco, et al.
American Journal of Medical Genetics. Part A|February 10, 2019
Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBPAndrea Angius, Paolo Uva, Manuela Oppo, et al.
Plos One|April 16, 2014
MxA mRNA quantification and disability progression in interferon beta-treated multiple sclerosis patientsFederico Serana, Luisa Imberti, Maria Pia Amato, et al.
Pageof 10

Showing results (61-70 of 93) with videos related to

Sort By:
Pageof 10
Journal of Neurology|May 9, 2003
Investigation of a genetic variation of a variable number tandem repeat polymorphism of interleukin-6 gene in patients with multiple sclerosisStephan Schmidt, Andreas Papassotiropoulos, Stefano Sotgiu, et al.
Cytokine|May 20, 2004
High frequency of TNF alleles -238A and -376A in individuals from northern SardiniaSebastian A Wirz, Maria C Morale, Bianca Marchetti, et al.
Microorganisms|January 25, 2025
HERVs Endophenotype in Autism Spectrum Disorder: Human Endogenous Retroviruses, Specific Immunoreactivity, and Disease Association in Different Family MembersMarco Bo, Alessandra Carta, Chiara Cipriani, et al.
Human Immunology|May 16, 2006
A family based linkage analysis of HLA and 5-HTTLPR gene polymorphisms in Sardinian children with autism spectrum disorderFranca R Guerini, Salvatorica Manca, Stefano Sotgiu, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|June 9, 2021
Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspringAlessandra Carta, Ignazio R Zarbo, Chiara Scoppola, et al.
Neuroscience|June 20, 2017
HLA-G∗14bp Insertion and the KIR2DS1-HLAC2 Complex Impact on Behavioral Impairment in Children with Autism Spectrum DisordersFranca R Guerini, Elisabetta Bolognesi, Matteo Chiappedi, et al.
Multiple Sclerosis and Related Disorders|March 10, 2024
Epidemiology of aquaporin-4-IgG-positive NMOSD in SardiniaElia Sechi, Mariangela Puci, Maria Ida Pateri, et al.
BMC Medical Genetics|May 9, 2019
VARS2-linked mitochondrial encephalopathy: two case reports enlarging the clinical phenotypeChiara Begliuomini, Giorgio Magli, Maja Di Rocco, et al.
American Journal of Medical Genetics. Part A|February 10, 2019
Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBPAndrea Angius, Paolo Uva, Manuela Oppo, et al.
Plos One|April 16, 2014
MxA mRNA quantification and disability progression in interferon beta-treated multiple sclerosis patientsFederico Serana, Luisa Imberti, Maria Pia Amato, et al.
Pageof 10