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Diagnóstico genético de pacientes con agammaglobulinemia primaria atendidos en centros peruanos de tercer nivel
(Instituto Nacional de Salud, 2020)
Las agammaglobulinemias primarias (AP) resultan de alteraciones específicas en las células B, lo cual, conduce a baja producción de anticuerpos. La sospecha diagnóstica se establece con el antecedente de infecciones a ...
Mutations of Bruton's tyrosine kinase gene in Brazilian patients with X-linked agammaglobulinemia
(Associação Brasileira de Divulgação Científica, 2010)
Mutations in Bruton's tyrosine kinase (BTK) gene are responsible for X-linked agammaglobulinemia (XLA), which is characterized by recurrent bacterial infections, profound hypogammaglobulinemia, and decreased numbers of ...
Defective Fc-, CR1- and CR3-mediated monocyte phagocytosis and chemotaxis in common variable immunodeficiency and X-linked agammaglobulinemia patients
(Hogrefe & Huber PublishersGottingenAlemanha, 2003)
Positive prick test in an x-linked agammaglobulinemia patient
(Elsevier B.V., 2007-01-01)
Arthritis associated with primary agammaglobulinemia: New clues to its immunopathology
Primary agammaglobulinemia is a rare disorder which is associated with articular symptoms in 11% of patients. Septic arthritis may occur, but often patients complain of chronic oligoarthritis and have a clinical presentation ...
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency
(2020)
Agammaglobulinemia is the most profound primary antibody deficiency that can occur due to an early termination of B-cell development. We here investigated three novel patients, including the first known adult, from unrelated ...