Virginie Grandin
Paris, France
Last Updated: 09/26/2026
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Found 8 publications
Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited.
Journal: Journal of clinical immunology
Published: July 05, 2022
Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencing.
Journal: The Journal of allergy and clinical immunology
Published: January 16, 2020
A deep intronic splice mutation of STAT3 underlies hyper IgE syndrome by negative dominance.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: July 27, 2019
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency.
Journal: Journal of clinical immunology
Published: May 11, 2018
Familial haemophagocytosis lymphohisticytosis type 3: A case report.
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: February 22, 2016
Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion.
Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: October 07, 2014
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey.
Journal: Medicine
Published: July 04, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026