BACKGROUND: Patients with adenosine deaminase 2 (ADA2) deficiency can present with various neurological manifestations due to vasculopathies and autoinflammation. These include ischemic and hemorrhagic stroke, but less clearly defined neurological symptoms have also been reported.METHODS: In this cohort study, we included patients with confirmed ADA2 deficiency from seven university hospitals in the Netherlands. We analyzed the frequency and recurrence rates of neurological manifestations before and after initiation of TNF-α inhibiting therapy.RESULTS: We included 29 patients with a median age at presentation of 5 years (IQR: 1-17). Neurological manifestations occurred in 19/29 (66%) patients and were the presenting symptom in 9/29 (31%) pa...
Adenosine deaminase (ADA) deficiency is one of the most prevalent forms of severe combined immunodef...
Deficiency of adenosine deaminase 2 (DADA2) is a unique monogenic autoinflammatory disease caused by...
Objective. To determine the genotype-phenotype association in patients with adenosine deaminase-2 (A...
BACKGROUND: Patients with adenosine deaminase 2 (ADA2) deficiency can present with various neurologi...
BACKGROUND: Patients with adenosine deaminase 2 (ADA2) deficiency can present with various neurologi...
Abstract Background Adenosine deaminase 2 (ADA2) deficiency is an inherited autoinflammatory syndrom...
SUMMARY: Adenosine deaminase 2 deficiency (OMIM #615688) is an autosomal recessive disorder characte...
Objectives T o analyse the prevalence of CECR1 mutations in patients diagnosed with early onset live...
Objectives\u2002To analyse the prevalence of CECR1 mutations in patients diagnosed with early onset ...
Funding Information: Funded by the Latvian Council of Science project grant Nr. lzp-2020/1–0269 and ...
Objective To describe the clinical features, genotype, and treatment in a series of subjects with c...
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessively inherited disease that h...
Objective To describe the clinical features, genotype, and treatment approaches of patients with con...
Adenosine deaminase 2 (ADA2) is an enzyme involved in purine metabolism and a growth factor that ...
Deficiency of ADA2 (DADA2) is the first molecularly described monogenic vasculitis syndrome. DADA2 i...
Adenosine deaminase (ADA) deficiency is one of the most prevalent forms of severe combined immunodef...
Deficiency of adenosine deaminase 2 (DADA2) is a unique monogenic autoinflammatory disease caused by...
Objective. To determine the genotype-phenotype association in patients with adenosine deaminase-2 (A...
BACKGROUND: Patients with adenosine deaminase 2 (ADA2) deficiency can present with various neurologi...
BACKGROUND: Patients with adenosine deaminase 2 (ADA2) deficiency can present with various neurologi...
Abstract Background Adenosine deaminase 2 (ADA2) deficiency is an inherited autoinflammatory syndrom...
SUMMARY: Adenosine deaminase 2 deficiency (OMIM #615688) is an autosomal recessive disorder characte...
Objectives T o analyse the prevalence of CECR1 mutations in patients diagnosed with early onset live...
Objectives\u2002To analyse the prevalence of CECR1 mutations in patients diagnosed with early onset ...
Funding Information: Funded by the Latvian Council of Science project grant Nr. lzp-2020/1–0269 and ...
Objective To describe the clinical features, genotype, and treatment in a series of subjects with c...
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessively inherited disease that h...
Objective To describe the clinical features, genotype, and treatment approaches of patients with con...
Adenosine deaminase 2 (ADA2) is an enzyme involved in purine metabolism and a growth factor that ...
Deficiency of ADA2 (DADA2) is the first molecularly described monogenic vasculitis syndrome. DADA2 i...
Adenosine deaminase (ADA) deficiency is one of the most prevalent forms of severe combined immunodef...
Deficiency of adenosine deaminase 2 (DADA2) is a unique monogenic autoinflammatory disease caused by...
Objective. To determine the genotype-phenotype association in patients with adenosine deaminase-2 (A...