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Last Updated: 10/31/2025
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Found 9 publications
Immune Reconstitution Inflammatory Syndrome After Hematopoietic Stem Cell Transplantation in a FOXN1 -deficient Patient.
Journal: Journal of pediatric hematology/oncology
Published: June 12, 2022
Spectrum of Genetic T-Cell Disorders from 22q11.2DS to CHARGE.
Journal: Clinical reviews in allergy & immunology
Published: January 13, 2022
Experience with cultured thymus tissue in 105 children.
Journal: The Journal of allergy and clinical immunology
Published: February 26, 2021
Congenital Athymia: Genetic Etiologies, Clinical Manifestations, Diagnosis, and Treatment.
Journal: Journal of clinical immunology
Published: January 04, 2021
Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.
Journal: American journal of human genetics
Published: April 19, 2019
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.
Journal: Journal of clinical immunology
Published: June 29, 2017
Neotenic phenomenon in gene expression in the skin of Foxn1- deficient (nude) mice - a projection for regenerative skin wound healing.
Journal: BMC genomics
Published: November 25, 2015
Post-thymus transplant vitiligo in a child with Foxn1 deficiency
Journal: Annales de dermatologie et de venereologie
Published: October 16, 2011
Showing 1-9 of 9
Last Updated: 10/31/2025