M. Louise Markert

Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients.

Corticosteroids regulate epithelial cell differentiation and Hassall body formation in the human thymus.

Postnatal thymus transplantation with immunosuppression as treatment for DiGeorge syndrome.

Complete DiGeorge syndrome: development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases.

Thymic transplantation for complete DiGeorge syndrome: medical and surgical considerations.

Statistical analysis of antigen receptor spectratype data.

SpA: web-accessible spectratype analysis: data management, statistical analysis and visualization.

Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants.

Long-term tolerance to allogeneic thymus transplants in complete DiGeorge anomaly.

Treatment of infants with complete DiGeorge anomaly.

Use of allograft biopsies to assess thymopoiesis after thymus transplantation.

Characterization of cultured thymus tissue used for transplantation with emphasis on promiscuous expression of thyroid tissue-specific genes.

Thymus transplantation in complete DiGeorge anomaly.

The dynamics of T-cell receptor repertoire diversity following thymus transplantation for DiGeorge anomaly.

Comèl-Netherton syndrome defined as primary immunodeficiency.

Thymus transplantation.

Mechanisms of tolerance to parental parathyroid tissue when combined with human allogeneic thymus transplantation.

First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases.

Successful extracorporeal membrane oxygenation for respiratory failure in an infant with DiGeorge anomaly, following thymus transplantation.

Induction of tolerance to parental parathyroid grafts using allogeneic thymus tissue in patients with DiGeorge anomaly.

Thymic microenvironment reconstitution after postnatal human thymus transplantation.

Interpreting low T-cell receptor excision circles in newborns with DiGeorge anomaly: importance of assessing naive T-cell markers.

Human FOXN1-deficiency is associated with αβ double-negative and FoxP3+ T-cell expansions that are distinctly modulated upon thymic transplantation.

Diagnosis of 22q11.2 deletion syndrome and artemis deficiency in two children with T-B-NK+ immunodeficiency.

Clinical course and outcome predictors of critically ill infants with complete DiGeorge anomaly following thymus transplantation.