Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Debray

Showing results (881-890 of 938) with videos related to

Pageof 94
Sort By:
Plos One|December 16, 2020
Glucocorticoids with low-dose anti-IL1 anakinra rescue in severe non-ICU COVID-19 infection: A cohort studyRaphael Borie, Laurent Savale, Antoine Dossier, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulationQuentin Riller, Boris Sorin, Charline Courteille, et al.
JHEP Reports : Innovation in Hepatology|January 18, 2024
Expert management of congenital portosystemic shunts and their complicationsValérie Anne McLin, Stéphanie Franchi-Abella, Timothée Brütsch, et al.
Brain : a Journal of Neurology|February 2, 2023
BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screeningTrine Tangeraas, Juliana R Constante, Paul Hoff Backe, et al.
The Annals of Thoracic Surgery|October 2, 2021
Diagnosis Yield and Safety of Surgical Biopsy in Interstitial Lung Diseases: A Prospective StudyDana Radu, Olivia Freynet, Marianne Kambouchner, et al.
European Journal of Human Genetics : EJHG|April 16, 2009
BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defectsEmma Hilton, Jennifer Johnston, Sandra Whalen, et al.
The Journal of Clinical Investigation|May 4, 2021
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammationEva Lausberg, Sebastian Gießelmann, Joseph P Dewulf, et al.
JHEP Reports : Innovation in Hepatology|March 14, 2024
Corrigendum to "Expert management of congenital portosystemic shunts and their complications" [JHEP Reports 6 (2024)]Valérie Anne McLin, Stéphanie Franchi-Abella, Timothée Brütsch, et al.
Scientific Data|March 2, 2026
Demographic, behavioral, and ecological data from a long-term field study of wild baboons in Amboseli, KenyaChelsea A Southworth, Jack C Winans, Jacob B Gordon, et al.
Radiology|June 29, 2021
Study of Thoracic CT in COVID-19: The STOIC ProjectMarie-Pierre Revel, Samia Boussouar, Constance de Margerie-Mellon, et al.
Pageof 94

Showing results (881-890 of 938) with videos related to

Sort By:
Pageof 94
Plos One|December 16, 2020
Glucocorticoids with low-dose anti-IL1 anakinra rescue in severe non-ICU COVID-19 infection: A cohort studyRaphael Borie, Laurent Savale, Antoine Dossier, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulationQuentin Riller, Boris Sorin, Charline Courteille, et al.
JHEP Reports : Innovation in Hepatology|January 18, 2024
Expert management of congenital portosystemic shunts and their complicationsValérie Anne McLin, Stéphanie Franchi-Abella, Timothée Brütsch, et al.
Brain : a Journal of Neurology|February 2, 2023
BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screeningTrine Tangeraas, Juliana R Constante, Paul Hoff Backe, et al.
The Annals of Thoracic Surgery|October 2, 2021
Diagnosis Yield and Safety of Surgical Biopsy in Interstitial Lung Diseases: A Prospective StudyDana Radu, Olivia Freynet, Marianne Kambouchner, et al.
European Journal of Human Genetics : EJHG|April 16, 2009
BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defectsEmma Hilton, Jennifer Johnston, Sandra Whalen, et al.
The Journal of Clinical Investigation|May 4, 2021
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammationEva Lausberg, Sebastian Gießelmann, Joseph P Dewulf, et al.
JHEP Reports : Innovation in Hepatology|March 14, 2024
Corrigendum to "Expert management of congenital portosystemic shunts and their complications" [JHEP Reports 6 (2024)]Valérie Anne McLin, Stéphanie Franchi-Abella, Timothée Brütsch, et al.
Scientific Data|March 2, 2026
Demographic, behavioral, and ecological data from a long-term field study of wild baboons in Amboseli, KenyaChelsea A Southworth, Jack C Winans, Jacob B Gordon, et al.
Radiology|June 29, 2021
Study of Thoracic CT in COVID-19: The STOIC ProjectMarie-Pierre Revel, Samia Boussouar, Constance de Margerie-Mellon, et al.
Pageof 94