Silvia Danielian

B, Argentina

Last Updated: 09/26/2026

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Found 24 publications

Disease-causing STAT3 variants can be discriminated by a functional flow cytometry test.

Disease-causing STAT3 variants can be discriminated by a functional flow cytometry test.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: September 15, 2025

In silico modeling guides identification of novel JAK1 variants associated with immune dysregulation.

In silico modeling guides identification of novel JAK1 variants associated with immune dysregulation.

Journal: EMBO molecular medicine

Published: April 09, 2025

Cancer Prevalence in Children with Inborn Errors of Immunity: Report from a Single Institution.

Cancer Prevalence in Children with Inborn Errors of Immunity: Report from a Single Institution.

Journal: Journal of clinical immunology

Published: July 27, 2023

Expanding spectrum, intrafamilial diversity, and therapeutic challenges from 15 patients with heterozygous CARD11-associated diseases: A single center experience.

Expanding spectrum, intrafamilial diversity, and therapeutic challenges from 15 patients with heterozygous CARD11-associated diseases: A single center experience.

Journal: Frontiers in immunology

Published: August 16, 2022

Disseminated BCG Disease in a Patient with Hyper IgE Syndrome due to Dominant-Negative STAT3 Mutation-Case Report.

Disseminated BCG Disease in a Patient with Hyper IgE Syndrome due to Dominant-Negative STAT3 Mutation-Case Report.

Journal: Journal of clinical immunology

Published: July 06, 2022

The interplay between serine proteases and caspase-1 regulates the autophagy-mediated secretion of Interleukin-1 beta in human neutrophils.

The interplay between serine proteases and caspase-1 regulates the autophagy-mediated secretion of Interleukin-1 beta in human neutrophils.

Journal: Frontiers in immunology

Published: December 09, 2021

Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 Deficiency.

Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 Deficiency.

Journal: Journal of clinical immunology

Published: November 28, 2021

Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence.

Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence.

Journal: Journal of clinical immunology

Published: September 28, 2021

Disseminated Bacillus Calmette-Guérin Infection in a Young Girl Leading to a Diagnosis of Immunodeficiency.

Disseminated Bacillus Calmette-Guérin Infection in a Young Girl Leading to a Diagnosis of Immunodeficiency.

Journal: Actas dermo-sifiliograficas

Published: August 07, 2021

Argentinian X-MAID Siblings with One of Them Manifesting a Rare Ophthalmological Complication.

Argentinian X-MAID Siblings with One of Them Manifesting a Rare Ophthalmological Complication.

Journal: Journal of clinical immunology

Published: April 27, 2021

Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects.

Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects.

Journal: Blood

Published: January 13, 2021

Correction to: A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency.

Correction to: A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency.

Journal: Journal of clinical immunology

Published: September 09, 2020

Showing 1-12 of 24

Last Updated: 09/26/2026