Cargando…
Germline biallelic PIK3CG mutations in a multifaceted immunodeficiency with immune dysregulation
Autores principales: | Thian, Marini, Hoeger, Birgit, Kamnev, Anton, Poyer, Fiona, Bal, Sevgi Köstel, Caldera, Michael, Jiménez-Heredia, Raúl, Huemer, Jakob, Pickl, Winfried F., Groß, Miriam, Ehl, Stephan, Lucas, Carrie L., Menche, Jörg, Hutter, Caroline, Attarbaschi, Andishe, Dupré, Loïc, Boztug, Kaan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Fondazione Ferrata Storti
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556668/ https://www.ncbi.nlm.nih.gov/pubmed/33054089 http://dx.doi.org/10.3324/haematol.2019.231399 |
Ejemplares similares
-
P1408: MONOALLELIC AND BIALLELIC GERMLINE MUTATIONS AFFECTING THE TRANSCRIPTION FACTOR HELIOS CAUSE PLEIOTROPIC DEFECTS OF IMMUNITY
por: Mayr, D., et al.
Publicado: (2022) -
Diagnosis and management of acute appendicitis in 21 pediatric hematology and oncology patients at a tertiary care cancer center
por: von Mersi, Hannah, et al.
Publicado: (2021) -
Human NF-κB1 Haploinsufficiency and Epstein–Barr Virus-Induced Disease—Molecular Mechanisms and Consequences
por: Hoeger, Birgit, et al.
Publicado: (2018) -
Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity
por: Willmann, Katharina L., et al.
Publicado: (2014) -
Relapsed acute lymphoblastic leukaemia after allogeneic stem cell
transplantation: a therapeutic dilemma challenging the armamentarium of
immunotherapies currently available (case reports)
por: Poyer, Fiona, et al.
Publicado: (2022)