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Nidia Moreno-Corona

Showing results (1-10 of 7) with videos related to

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Frontiers in Pediatrics|July 12, 2021
Activated PI3Kinase Delta Syndrome-A Multifaceted DiseaseRomane Thouenon, Nidia Moreno-Corona, Lucie Poggi, et al.
Journal of Clinical Immunology|July 31, 2023
A Case Report of Folliculin-Interacting Protein 1 DeficiencyNidia Moreno-Corona, Alice Valagussa, Romane Thouenon, et al.
Journal of Human Immunity|January 30, 2026
A heterozygous USB1 variant linked to immunodeficiencyAlice Valagussa, Nidia Moreno-Corona, Chantal Lagresle-Peyrou, et al.
Frontiers in Pediatrics|July 12, 2021
Two Monogenetic Disorders, Activated PI3-Kinase-δ Syndrome 2 and Smith-Magenis Syndrome, in One Patient: Case Report and a Literature Review of Neurodevelopmental Impact in Primary Immunodeficiencies Associated With Disturbed PI3K SignalingNidia Moreno-Corona, Loïc Chentout, Lucie Poggi, et al.
Journal of Human Immunity|May 8, 2026
Ribosomal RNA processing impairments in a B cell immunodeficient patient with WDR75 variantsNidia Moreno-Corona, Alice Valagussa, Lucie Poggi, et al.
The Journal of Experimental Medicine|March 14, 2023
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiencyRomane Thouenon, Loïc Chentout, Nidia Moreno-Corona, et al.
Science Immunology|January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency, Oriol Fornes, Alicia Jia, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Frontiers in Pediatrics|July 12, 2021
Activated PI3Kinase Delta Syndrome-A Multifaceted DiseaseRomane Thouenon, Nidia Moreno-Corona, Lucie Poggi, et al.
Journal of Clinical Immunology|July 31, 2023
A Case Report of Folliculin-Interacting Protein 1 DeficiencyNidia Moreno-Corona, Alice Valagussa, Romane Thouenon, et al.
Journal of Human Immunity|January 30, 2026
A heterozygous USB1 variant linked to immunodeficiencyAlice Valagussa, Nidia Moreno-Corona, Chantal Lagresle-Peyrou, et al.
Frontiers in Pediatrics|July 12, 2021
Two Monogenetic Disorders, Activated PI3-Kinase-δ Syndrome 2 and Smith-Magenis Syndrome, in One Patient: Case Report and a Literature Review of Neurodevelopmental Impact in Primary Immunodeficiencies Associated With Disturbed PI3K SignalingNidia Moreno-Corona, Loïc Chentout, Lucie Poggi, et al.
Journal of Human Immunity|May 8, 2026
Ribosomal RNA processing impairments in a B cell immunodeficient patient with WDR75 variantsNidia Moreno-Corona, Alice Valagussa, Lucie Poggi, et al.
The Journal of Experimental Medicine|March 14, 2023
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiencyRomane Thouenon, Loïc Chentout, Nidia Moreno-Corona, et al.
Science Immunology|January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency, Oriol Fornes, Alicia Jia, et al.
Pageof 1