Hans C. Erichsen

Oslo, 0318, Norway

Last Updated: 09/26/2026

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Found 13 publications

Precision T cell correction platform for inborn errors of immunity.

Precision T cell correction platform for inborn errors of immunity.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: February 14, 2025

Genetic and clinical characteristics of patients with Shwachman Diamond syndrome with special consideration of treatment with granulocyte-colony stimulating factor.

Genetic and clinical characteristics of patients with Shwachman Diamond syndrome with special consideration of treatment with granulocyte-colony stimulating factor.

Journal: Haematologica

Published: June 27, 2024

NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

Journal: Science immunology

Published: May 24, 2024

Primary antibody deficiency: The impact on the quality of life and mental health of affected children and their parents.

Primary antibody deficiency: The impact on the quality of life and mental health of affected children and their parents.

Journal: Acta paediatrica (Oslo, Norway : 1992)

Published: July 02, 2020

Second-Tier Next Generation Sequencing Integrated in Nationwide Newborn Screening Provides Rapid Molecular Diagnostics of Severe Combined Immunodeficiency.

Second-Tier Next Generation Sequencing Integrated in Nationwide Newborn Screening Provides Rapid Molecular Diagnostics of Severe Combined Immunodeficiency.

Journal: Frontiers in immunology

Published: March 24, 2020

A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function.

A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function.

Journal: The Journal of experimental medicine

Published: January 23, 2019

Allogeneic hematopoietic stem cell transplant outcomes for patients with dominant negative IKZF1/IKAROS mutations.

Allogeneic hematopoietic stem cell transplant outcomes for patients with dominant negative IKZF1/IKAROS mutations.

Journal: The Journal of allergy and clinical immunology

Published: December 05, 2018

A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency.

A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency.

Journal: The Journal of allergy and clinical immunology

Published: September 10, 2018

Thymus transplantation for complete DiGeorge syndrome: European experience.

Thymus transplantation for complete DiGeorge syndrome: European experience.

Journal: The Journal of allergy and clinical immunology

Published: July 08, 2016

A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction.

A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction.

Journal: Molecular genetics & genomic medicine

Published: June 14, 2016

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.

Journal: The Journal of allergy and clinical immunology

Published: February 02, 2016

Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis.

Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis.

Journal: Genome medicine

Published: August 26, 2015

Showing 1-12 of 13

Last Updated: 09/26/2026