Teresa K Tarrant

17PUBLICATIONS
131CO-AUTHORS
Gene and molecular therapyGene expression (incl. microarray and other genome-wide approaches)Infant and child healthNeonatologyDisease surveillance
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Publications (17)

|Jul 22, 2026
A case of progressive multifocal leukoencephalopathy in an adult patient with ADA-SCID.

|Jun 18, 2026
ADA2 genotype and enzyme activity may predict vasculitic or hematologic DADA2 phenotype.

|May 22, 2026
Early identification of delayed-onset ADA deficiency: The case for expanded first-tier newborn screening.

|May 05, 2025
Comment on: Use of Plerixafor for Short-Term Management of Leukopenia in a Pediatric Patient With WHIM Syndrome.

Julia T Warren, Christophe Arbet-Engels, Deborah J Steiner

|Mar 27, 2025
Multi-Year Registry Study of Elapegademase Treatment in Patients With Adenosine Deaminase Severe Combined Immunodeficiency (ADA-SCID) Requiring Enzyme Replacement Therapy.

Morna J Dorsey, Manish J Butte, Jay A Lieberman

|May 20, 2024
A novel transmembrane CXCR4 variant that expands the WHIM genotype-phenotype paradigm.

Katarina Zmajkovicova, Sumit Pawar, Svetlana O Sharapova

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Frequent Collaborators

5 joint publications

Michael S Hershfield

2 joint publications

Jolan E Walter

2 joint publications

Bodo Grimbacher

2 joint publications

David S Lawrence