Heterozygous Mutation in Adenosine Deaminase Gene in a Patient With Severe Lymphopenia Following Corticosteroid Treatment of Autoimmune Hemolytic Anemia

Author:

Tripodi Serena I.,Corti Paola,Giliani Silvia,Lanfranchi Arnalda,Biondi Andrea,Badolato Raffaele

Funder

Ministero della Salute

Publisher

Frontiers Media SA

Subject

Pediatrics, Perinatology and Child Health

Reference25 articles.

1. Isozymes of adenosine deaminase;Hirschhorn;Isozymes Curr Top Biol Med Res,1980

2. Pathologic findings in adenosine deaminase-deficient severe combined immunodeficiency. I. Kidney, adrenal, and chondro-osseous tissue alterations;Ratech;Am J Pathol,1989

3. Adenosine-deaminase deficiency in two patients with severely impaired cellular immunity;Giblett;Lancet,1972

4. Adenosine deaminase deficient severe combined immunodeficiency presenting as atypical haemolytic uraemic syndrome;Nikolajeva;J Clin Immunol,2015

5. Diagnosis, treatment and long-term follow up of patients with ADA deficiency: a single-center experience;Baffelli;J Clin Immunol.,2015

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