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The Journal of Clinical Investigation
|
October 21, 2021
Will GWAS eventually allow the identification of genomic biomarkers for COVID-19 severity and mortality?
Vito Luigi Colona, Michela Biancolella, Antonio Novelli, et al.
Brain Sciences
|
November 25, 2023
A New Case of Autosomal-Dominant <i>POLR3B</i>-Related Disorder: Widening Genotypic and Phenotypic <i>Spectrum</i>
Vito Luigi Colona, Enrico Bertini, Maria Cristina Digilio, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
June 17, 2017
Assessment of serum uric acid as risk factor for tauopathies
Tommaso Schirinzi, Giulia Di Lazzaro, Vito Luigi Colona, et al.
Human Genomics
|
June 1, 2022
COVID-19 2022 update: transition of the pandemic to the endemic phase
Michela Biancolella, Vito Luigi Colona, Ruty Mehrian-Shai, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 17, 2025
Genotype variability in early-onset Hereditary Spastic Paraplegia: a single-center study
Vito Luigi Colona, Lorena Travaglini, Jacopo Sartorelli, et al.
Parkinsonism & Related Disorders
|
October 24, 2018
CSF α-synuclein inversely correlates with non-motor symptoms in a cohort of PD patients
Tommaso Schirinzi, Giulia Maria Sancesario, Giulia Di Lazzaro, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
September 4, 2017
Levels of amyloid-beta-42 and CSF pressure are directly related in patients with Alzheimer's disease
Tommaso Schirinzi, Giulia Di Lazzaro, Giulia Maria Sancesario, et al.
Brain Sciences
|
February 26, 2025
Three Cases of Spinocerebellar Ataxia Type 2 (SCA2) and Pediatric Literature Review: Do Not Forget Trinucleotide Repeat Disorders in Childhood-Onset Progressive Ataxia
Jacopo Sartorelli, Maria Grazia Pomponi, Giacomo Garone, et al.
Cerebellum (London, England)
|
September 23, 2024
De Novo GRID2 Variant as a Cause of Ataxia with Oculomotor Apraxia and Alpha-Fetoprotein Elevation
Jacopo Sartorelli, Lorena Travaglini, Vito Luigi Colona, et al.
Human Genomics
|
May 10, 2021
COVID-19 one year into the pandemic: from genetics and genomics to therapy, vaccination, and policy
Giuseppe Novelli, Michela Biancolella, Ruty Mehrian-Shai, et al.
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Search research articles
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Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
The Journal of Clinical Investigation
|
October 21, 2021
Will GWAS eventually allow the identification of genomic biomarkers for COVID-19 severity and mortality?
Vito Luigi Colona, Michela Biancolella, Antonio Novelli, et al.
Brain Sciences
|
November 25, 2023
A New Case of Autosomal-Dominant <i>POLR3B</i>-Related Disorder: Widening Genotypic and Phenotypic <i>Spectrum</i>
Vito Luigi Colona, Enrico Bertini, Maria Cristina Digilio, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
June 17, 2017
Assessment of serum uric acid as risk factor for tauopathies
Tommaso Schirinzi, Giulia Di Lazzaro, Vito Luigi Colona, et al.
Human Genomics
|
June 1, 2022
COVID-19 2022 update: transition of the pandemic to the endemic phase
Michela Biancolella, Vito Luigi Colona, Ruty Mehrian-Shai, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 17, 2025
Genotype variability in early-onset Hereditary Spastic Paraplegia: a single-center study
Vito Luigi Colona, Lorena Travaglini, Jacopo Sartorelli, et al.
Parkinsonism & Related Disorders
|
October 24, 2018
CSF α-synuclein inversely correlates with non-motor symptoms in a cohort of PD patients
Tommaso Schirinzi, Giulia Maria Sancesario, Giulia Di Lazzaro, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
September 4, 2017
Levels of amyloid-beta-42 and CSF pressure are directly related in patients with Alzheimer's disease
Tommaso Schirinzi, Giulia Di Lazzaro, Giulia Maria Sancesario, et al.
Brain Sciences
|
February 26, 2025
Three Cases of Spinocerebellar Ataxia Type 2 (SCA2) and Pediatric Literature Review: Do Not Forget Trinucleotide Repeat Disorders in Childhood-Onset Progressive Ataxia
Jacopo Sartorelli, Maria Grazia Pomponi, Giacomo Garone, et al.
Cerebellum (London, England)
|
September 23, 2024
De Novo GRID2 Variant as a Cause of Ataxia with Oculomotor Apraxia and Alpha-Fetoprotein Elevation
Jacopo Sartorelli, Lorena Travaglini, Vito Luigi Colona, et al.
Human Genomics
|
May 10, 2021
COVID-19 one year into the pandemic: from genetics and genomics to therapy, vaccination, and policy
Giuseppe Novelli, Michela Biancolella, Ruty Mehrian-Shai, et al.
Page
of 4