Yulia A. Rodina

Moscow, MOW 117198, Russian Federation

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 36 publications

Optimizing Kappa-Deleting Recombination Excision Circles (KREC) Cut-Off Values in Russian Newborn Screening Program: Balancing Sensitivity and False-Positive Rates.

Optimizing Kappa-Deleting Recombination Excision Circles (KREC) Cut-Off Values in Russian Newborn Screening Program: Balancing Sensitivity and False-Positive Rates.

Journal: International journal of neonatal screening

Published: March 30, 2026

Diagnostic workflow for X-linked agammaglobulinemia integrating BTK expression and B-cell maturation analysis by flow cytometry.

Diagnostic workflow for X-linked agammaglobulinemia integrating BTK expression and B-cell maturation analysis by flow cytometry.

Journal: Cytometry. Part B, Clinical cytometry

Published: February 26, 2026

First 2-year experience of nationwide newborn screening for severe forms of T and B cell immunodeficiency: 2.3 million newborns analyzed using TREC and KREC in Russia.

First 2-year experience of nationwide newborn screening for severe forms of T and B cell immunodeficiency: 2.3 million newborns analyzed using TREC and KREC in Russia.

Journal: Frontiers in immunology

Published: November 09, 2025

Development, Validation, and Clinical Application of an HPLC-Based Method for Determining Adenosine Deaminase Activity in Adenosine Deaminase Deficiency-Severe Combined Immunodeficiency.

Development, Validation, and Clinical Application of an HPLC-Based Method for Determining Adenosine Deaminase Activity in Adenosine Deaminase Deficiency-Severe Combined Immunodeficiency.

Journal: The journal of applied laboratory medicine

Published: October 16, 2025

Recurrent acute liver failure and neutropenia caused by a novel homozygous RINT1 variant: a brief report of phenotypic expansion and population-specific findings.

Recurrent acute liver failure and neutropenia caused by a novel homozygous RINT1 variant: a brief report of phenotypic expansion and population-specific findings.

Journal: Human genomics

Published: June 30, 2025

Clinical experience with emapalumab treatment in a group of children with primary hemophagocytic lymphohistiocytosis.

Clinical experience with emapalumab treatment in a group of children with primary hemophagocytic lymphohistiocytosis.

Journal: Journal of human immunity

Published: June 21, 2025

Different Diagnoses, Common Ancestry: 22q11.2 Deletion Syndrome and Wiskott-Aldrich Syndrome in the Same Family.

Different Diagnoses, Common Ancestry: 22q11.2 Deletion Syndrome and Wiskott-Aldrich Syndrome in the Same Family.

Journal: Molecular syndromology

Published: June 05, 2025

Harmonizing TREC Thresholds in Newborn Screening for SCID: Insights From Russian Validation Cohort.

Harmonizing TREC Thresholds in Newborn Screening for SCID: Insights From Russian Validation Cohort.

Journal: Journal of clinical laboratory analysis

Published: April 09, 2025

Рrospective multicenter study of treatment efficacy, safety, and quality of life in a large cohort of patients with inborn errors of immunity receiving subcutaneous immunoglobulin by the rapid push method.

Рrospective multicenter study of treatment efficacy, safety, and quality of life in a large cohort of patients with inborn errors of immunity receiving subcutaneous immunoglobulin by the rapid push method.

Journal: Frontiers in immunology

Published: March 23, 2025

Efficacy and safety of romiplostim and eltrombopag in management of thrombocytopenia in Wiskott-Aldrich syndrome patients.

Efficacy and safety of romiplostim and eltrombopag in management of thrombocytopenia in Wiskott-Aldrich syndrome patients.

Journal: British journal of haematology

Published: March 05, 2025

Novel LYST Variants Lead to Aberrant Splicing in a Patient with Chediak-Higashi Syndrome.

Novel LYST Variants Lead to Aberrant Splicing in a Patient with Chediak-Higashi Syndrome.

Journal: Genes

Published: December 03, 2024

A Rare Case of TP63-Associated Lymphopenia Revealed by Newborn Screening Using TREC.

A Rare Case of TP63-Associated Lymphopenia Revealed by Newborn Screening Using TREC.

Journal: International journal of molecular sciences

Published: September 15, 2024

Showing 1-12 of 36

Last Updated: 09/26/2026