Raul Heredia-Jimenez
Vienna, Austria
Last Updated: 09/26/2026
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Found 23 publications
Image-based drug screening combined with molecular profiling identifies signatures and drivers of therapy resistance in pediatric AML.
Journal: Cell reports. Medicine
Published: November 28, 2024
Clinical and Immunological Prognostic Factors With Novel Variants in a Large Cohort of Diacylglycerol Acyltransferase 1 Deficiency.
Journal: The journal of allergy and clinical immunology. In practice
Published: November 28, 2024
Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome.
Journal: Research square
Published: September 18, 2023
A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes.
Journal: HemaSphere
Published: August 02, 2023
Systemic Inflammation and Normocytic Anemia in DOCK11 Deficiency.
Journal: The New England journal of medicine
Published: June 21, 2023
Novel CARMIL2 (RLTPR) Mutation Presenting with Hyper-IgE and Eosinophilia: A Case Report.
Journal: Endocrine, metabolic & immune disorders drug targets
Published: May 20, 2023
Evans syndrome caused by a deleterious mutation affecting the adaptor protein SASH3.
Journal: British journal of haematology
Published: April 23, 2023
Phosphomevalonate kinase deficiency expands the genetic spectrum of systemic autoinflammatory diseases.
Journal: The Journal of allergy and clinical immunology
Published: February 01, 2023
Case Report: Refractory Cytopenia With a Switch From a Transient Monosomy 7 to a Disease-Ameliorating del(20q) in a NHEJ1-Deficient Long-term Survivor.
Journal: Frontiers in immunology
Published: February 03, 2022
Identification of germline monoallelic mutations in IKZF2 in patients with immune dysregulation.
Journal: Blood advances
Published: October 14, 2021
Last Updated: 09/26/2026