Adenosine deaminase (ADA) deficiency is best known as a form of severe combined immunodeficiency (SCID) that results from mutations in the gene encoding ADA. Affected patients present with clinical and immunological manifestations typical of a SCID. Therapies are currently available that can target these immunological disturbances and treated patients show varying degrees of clinical improvement. However, there is now a growing body of evidence that deficiency of ADA has significant impact on non-immunological organ systems. This review will outline the impact of ADA deficiency on various organ systems, starting with the well-understood immunological abnormalities. We will discuss possible pathogenic mechanisms and also highlight ways in wh...
A deficiency of the enzyme adenosine deaminase is associated with an autosomal recessive form of sev...
We describe a previously healthy 14-year-old girl with acute onset autoimmune hemolytic anemia, asso...
Objective To describe the clinical features, genotype, and treatment in a series of subjects with c...
Adenosine deaminase (ADA) deficiency is one of the most prevalent forms of severe combined immunodef...
Adenosine deaminase 1 [ADA] deficiency is a very rare condition inherited in an autosomal recessive ...
Adenosine Desaminase (ADA) deficiency, is a purine metabolic disorder that cause severe combined imm...
Adenosine deaminase (ADA) deficiency is an autosomal recessive primary immunodeficiency. It results ...
SummaryAdenosine deaminase (ADA) deficiency causes lymphopenia and immunodeficiency due to toxic eff...
PURPOSE OF REVIEW: Adenosine deaminase (ADA)- deficient severe combined immunodeficiency (SCID) is ...
Adenosine deaminase (ADA) is a purine metabolism enzyme that catalyses the breakdown of adenosine an...
Deficiency of adenosine deaminase (ADA, EC3.5.4.4), a housekeeping enzyme intrinsic to the purine sa...
Human adenosine deaminase 1 deficiency was described in the 1970s to cause severe combined immunodef...
Abstract Adenosine deaminase (ADA) deficiency leads to an accumulation of toxic purine degradation b...
adenosine deaminase (ADA) results in a syndrome of severe combined immunodeficiency (SCID). Children...
Background: We investigated the long-term outcome of gene therapy for severe combined immunodeficien...
A deficiency of the enzyme adenosine deaminase is associated with an autosomal recessive form of sev...
We describe a previously healthy 14-year-old girl with acute onset autoimmune hemolytic anemia, asso...
Objective To describe the clinical features, genotype, and treatment in a series of subjects with c...
Adenosine deaminase (ADA) deficiency is one of the most prevalent forms of severe combined immunodef...
Adenosine deaminase 1 [ADA] deficiency is a very rare condition inherited in an autosomal recessive ...
Adenosine Desaminase (ADA) deficiency, is a purine metabolic disorder that cause severe combined imm...
Adenosine deaminase (ADA) deficiency is an autosomal recessive primary immunodeficiency. It results ...
SummaryAdenosine deaminase (ADA) deficiency causes lymphopenia and immunodeficiency due to toxic eff...
PURPOSE OF REVIEW: Adenosine deaminase (ADA)- deficient severe combined immunodeficiency (SCID) is ...
Adenosine deaminase (ADA) is a purine metabolism enzyme that catalyses the breakdown of adenosine an...
Deficiency of adenosine deaminase (ADA, EC3.5.4.4), a housekeeping enzyme intrinsic to the purine sa...
Human adenosine deaminase 1 deficiency was described in the 1970s to cause severe combined immunodef...
Abstract Adenosine deaminase (ADA) deficiency leads to an accumulation of toxic purine degradation b...
adenosine deaminase (ADA) results in a syndrome of severe combined immunodeficiency (SCID). Children...
Background: We investigated the long-term outcome of gene therapy for severe combined immunodeficien...
A deficiency of the enzyme adenosine deaminase is associated with an autosomal recessive form of sev...
We describe a previously healthy 14-year-old girl with acute onset autoimmune hemolytic anemia, asso...
Objective To describe the clinical features, genotype, and treatment in a series of subjects with c...