Daniela S. Iancu

Southampton, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 30 publications

Erythromelalgia in a Child With a KIF2A Mutation.

Erythromelalgia in a Child With a KIF2A Mutation.

Journal: Clinical and experimental dermatology

Published: March 31, 2026

A multi-national study examined the response sustainability to calcineurin inhibitors and long-term kidney survivals in children with genetic podocytopathies.

A multi-national study examined the response sustainability to calcineurin inhibitors and long-term kidney survivals in children with genetic podocytopathies.

Journal: Kidney international

Published: November 07, 2025

A multi-national study examined the response sustainability to calcineurin inhibitors and long-term kidney survivals in children with genetic podocytopathies.

A multi-national study examined the response sustainability to calcineurin inhibitors and long-term kidney survivals in children with genetic podocytopathies.

Journal: Kidney international

Published: November 07, 2025

Tuning antibody stability and function by rational designs of framework mutations.

Tuning antibody stability and function by rational designs of framework mutations.

Journal: mAbs

Published: July 14, 2025

Duchenne and Becker Muscular Dystrophies in Romania: a 10-year Retrospective Study.

Duchenne and Becker Muscular Dystrophies in Romania: a 10-year Retrospective Study.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: May 23, 2025

Ethical implications of developing RNA-based therapies for cardiovascular disorders.

Ethical implications of developing RNA-based therapies for cardiovascular disorders.

Journal: Frontiers in bioengineering and biotechnology

Published: January 14, 2024

Corrigendum to "A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants." Kidney Int. 2023;103:962-972.

Corrigendum to "A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants." Kidney Int. 2023;103:962-972.

Journal: Kidney international

Published: January 05, 2024

De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome.

De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome.

Journal: Brain : a journal of neurology

Published: November 02, 2023

Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic Patients.

Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic Patients.

Journal: Kidney international reports

Published: October 03, 2022

A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants.

A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants.

Journal: Kidney international

Published: May 11, 2022

A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.

A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.

Journal: Journal of the American Society of Nephrology : JASN

Published: October 06, 2021

ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature.

ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature.

Journal: American journal of medical genetics. Part A

Published: March 01, 2021

Showing 1-12 of 30

Last Updated: 09/26/2026