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Sandra Salem

Showing results (1-10 of 9) with videos related to

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Human Genetics|April 2, 2020
Role of IRF8 in immune cells functions, protection against infections, and susceptibility to inflammatory diseasesSandra Salem, David Salem, Philippe Gros
BMC Nephrology|October 16, 2025
Real-world burden of primary hyperoxaluria with chronic kidney disease in the United States: a retrospective administrative claims analysisDavid S Goldfarb, Frank Modersitzki, Jeffrey R Skaar, et al.
Orphanet Journal of Rare Diseases|May 14, 2025
Treatment preferences among individuals with primary hyperoxaluria type 1 (PH1): a real-world studyDavid S Goldfarb, Jing Voon Chen, Rebekah Zincavage, et al.
Journal of Cellular and Molecular Medicine|June 24, 2014
A novel role for interferon regulatory factor 1 (IRF1) in regulation of bone metabolismSandra Salem, Chan Gao, Ailian Li, et al.
Mindfulness|January 25, 2020
MYmind: a Concurrent Group-Based Mindfulness Intervention for Youth with Autism and Their ParentsSandra Salem-Guirgis, Carly Albaum, Paula Tablon, et al.
Human Mutation|March 26, 2009
Novel mutations in VANGL1 in neural tube defectsZoha Kibar, Ciprian M Bosoi, Megan Kooistra, et al.
Blood|August 15, 2014
Functional characterization of the human dendritic cell immunodeficiency associated with the IRF8(K108E) mutationSandra Salem, David Langlais, François Lefebvre, et al.
Science (New York, N.Y.)|August 4, 2012
Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiencyDusan Bogunovic, Minji Byun, Larissa A Durfee, et al.
The New England Journal of Medicine|April 29, 2011
IRF8 mutations and human dendritic-cell immunodeficiencySophie Hambleton, Sandra Salem, Jacinta Bustamante, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Human Genetics|April 2, 2020
Role of IRF8 in immune cells functions, protection against infections, and susceptibility to inflammatory diseasesSandra Salem, David Salem, Philippe Gros
BMC Nephrology|October 16, 2025
Real-world burden of primary hyperoxaluria with chronic kidney disease in the United States: a retrospective administrative claims analysisDavid S Goldfarb, Frank Modersitzki, Jeffrey R Skaar, et al.
Orphanet Journal of Rare Diseases|May 14, 2025
Treatment preferences among individuals with primary hyperoxaluria type 1 (PH1): a real-world studyDavid S Goldfarb, Jing Voon Chen, Rebekah Zincavage, et al.
Journal of Cellular and Molecular Medicine|June 24, 2014
A novel role for interferon regulatory factor 1 (IRF1) in regulation of bone metabolismSandra Salem, Chan Gao, Ailian Li, et al.
Mindfulness|January 25, 2020
MYmind: a Concurrent Group-Based Mindfulness Intervention for Youth with Autism and Their ParentsSandra Salem-Guirgis, Carly Albaum, Paula Tablon, et al.
Human Mutation|March 26, 2009
Novel mutations in VANGL1 in neural tube defectsZoha Kibar, Ciprian M Bosoi, Megan Kooistra, et al.
Blood|August 15, 2014
Functional characterization of the human dendritic cell immunodeficiency associated with the IRF8(K108E) mutationSandra Salem, David Langlais, François Lefebvre, et al.
Science (New York, N.Y.)|August 4, 2012
Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiencyDusan Bogunovic, Minji Byun, Larissa A Durfee, et al.
The New England Journal of Medicine|April 29, 2011
IRF8 mutations and human dendritic-cell immunodeficiencySophie Hambleton, Sandra Salem, Jacinta Bustamante, et al.
Pageof 1