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Frontiers in Psychiatry
|
January 30, 2024
<i>PTCHD1</i> gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports
Federica Alice Maria Montanaro, Alessandra Mandarino, Viola Alesi, et al.
Ebiomedicine
|
September 4, 2018
Assessing statin effects on cardiovascular pathways in HIV using a novel proteomics approach: Analysis of data from INTREPID, a randomized controlled trial
Mabel Toribio, Kathleen V Fitch, Lauren Stone, et al.
JACC. Heart Failure
|
August 12, 2019
The Risk for Sudden Cardiac Death Among Patients Living With Heart Failure and Human Immunodeficiency Virus
Raza M Alvi, Anne M Neilan, Noor Tariq, et al.
Annals of Human Genetics
|
October 16, 2010
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities
Tiziana Bachetti, Eleonora Di Zanni, Francesca Lantieri, et al.
Journal of Medical Genetics
|
September 11, 2025
Further evidence of <i>RNU4ATAC</i> variants causing Joubert syndrome with skeletal involvement
Fulvio D'Abrusco, Simone Gana, Enrico Alfei, et al.
Viruses
|
September 27, 2025
Human-Derived H3N2 Influenza A Viruses Detected in Pigs in Northern Italy
Laura Soliani, Ada Mescoli, Irene Zanni, et al.
European Heart Journal. Acute Cardiovascular Care
|
September 14, 2023
Air pollution and out-of-hospital cardiac arrest risk: a 7-year study from a highly polluted area
Luca Moderato, Daniela Aschieri, Davide Lazzeroni, et al.
Frontiers in Psychiatry
|
February 28, 2024
Corrigendum: PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports
Federica Alice Maria Montanaro, Alessandra Mandarino, Viola Alesi, et al.
AIDS (London, England)
|
June 18, 2016
Subclinical myocyte injury, fibrosis and strain in relationship to coronary plaque in asymptomatic HIV-infected individuals
Kathleen V Fitch, Christopher DeFilippi, Robert Christenson, et al.
Neurogenetics
|
April 26, 2018
The impact of next-generation sequencing on the diagnosis of pediatric-onset hereditary spastic paraplegias: new genotype-phenotype correlations for rare HSP-related genes
Lorena Travaglini, Chiara Aiello, Fabrizia Stregapede, et al.
Page
of 95
Search research articles
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Showing results (741-750 of 943) with videos related to
Sort By:
Page
of 95
Frontiers in Psychiatry
|
January 30, 2024
<i>PTCHD1</i> gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports
Federica Alice Maria Montanaro, Alessandra Mandarino, Viola Alesi, et al.
Ebiomedicine
|
September 4, 2018
Assessing statin effects on cardiovascular pathways in HIV using a novel proteomics approach: Analysis of data from INTREPID, a randomized controlled trial
Mabel Toribio, Kathleen V Fitch, Lauren Stone, et al.
JACC. Heart Failure
|
August 12, 2019
The Risk for Sudden Cardiac Death Among Patients Living With Heart Failure and Human Immunodeficiency Virus
Raza M Alvi, Anne M Neilan, Noor Tariq, et al.
Annals of Human Genetics
|
October 16, 2010
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities
Tiziana Bachetti, Eleonora Di Zanni, Francesca Lantieri, et al.
Journal of Medical Genetics
|
September 11, 2025
Further evidence of <i>RNU4ATAC</i> variants causing Joubert syndrome with skeletal involvement
Fulvio D'Abrusco, Simone Gana, Enrico Alfei, et al.
Viruses
|
September 27, 2025
Human-Derived H3N2 Influenza A Viruses Detected in Pigs in Northern Italy
Laura Soliani, Ada Mescoli, Irene Zanni, et al.
European Heart Journal. Acute Cardiovascular Care
|
September 14, 2023
Air pollution and out-of-hospital cardiac arrest risk: a 7-year study from a highly polluted area
Luca Moderato, Daniela Aschieri, Davide Lazzeroni, et al.
Frontiers in Psychiatry
|
February 28, 2024
Corrigendum: PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports
Federica Alice Maria Montanaro, Alessandra Mandarino, Viola Alesi, et al.
AIDS (London, England)
|
June 18, 2016
Subclinical myocyte injury, fibrosis and strain in relationship to coronary plaque in asymptomatic HIV-infected individuals
Kathleen V Fitch, Christopher DeFilippi, Robert Christenson, et al.
Neurogenetics
|
April 26, 2018
The impact of next-generation sequencing on the diagnosis of pediatric-onset hereditary spastic paraplegias: new genotype-phenotype correlations for rare HSP-related genes
Lorena Travaglini, Chiara Aiello, Fabrizia Stregapede, et al.
Page
of 95