Disease: Agammaglobulinemia- non-Bruton type
- A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project
- Autosomal Recessive Agammaglobulinemia - first case with a novel TCF3 mutation from Pakistan
- Autosomal Recessive Agammaglobulinemia Due to a Homozygous Mutation in PIK3R1
- Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a
- Autosomal recessive agammaglobulinemia: the third case of Igbeta deficiency due to a novel non-sense mutation
- Autosomal recessive agammaglobulinemia: the third case of Igβ deficiency due to a novel non-sense mutation
- Efficacy and safety of Gammaplex(®) 5% in children and adolescents with primary immunodeficiency diseases
- Efficacy and safety of Hizentra(®) in patients with primary immunodeficiency after a dose-equivalent switch from intravenous or subcutaneous replacement therapy
- Evaluation of B lymphocyte deficiencies
- Evaluation of respiratory complications in patients with X-linked and autosomal recessive agammaglobulinemia
- Gastrectomy with isoperistaltic jejunal parallel pouch in a 15-year-old adolescent boy with gastric adenocarcinoma and autosomal recessive agammaglobulinemia
- Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study