Forty years after Bruton's discovery, the spectrum of primary defects of immunoglobulins has been largely extended and characterized. An increasingly more accurate recognition of the basic pathogenetic mechanisms of disease has helped to design more effective drugs and therapeutic strategies for patients with both primary and secondary immune deficiencies. In recent years, major advances in molecular biology have allowed characterization of the genetic basis of many primary immunodeficiencies, resulting in more accurate genetic counseling and leading to the first successful application of genetic therapy to the treatment of a human disease
Mutation pattern was characterized in the Bruton's tyrosine kinase gene (BTK) in 26 patients with X-...
Introduction: X-linked agammaglobulinemia (XLA) is the most common primary immunodeficiency in man, ...
Genetic testing has become important in the repertoire for the diagnosis of primary immunodeficienci...
Primary antibody deficiencies represent the most frequent genetic diseases of the immune system and ...
More than 50 years after Ogdeon Bruton's discovery of congenital agammaglobulinemia, human primary i...
La agammaglobulinemia ligada al X o de Bruton constituye el prototipo de deficiencia primaria de cél...
In the last fifteen years, therapeutic use of intravenous immunoglobulin on one hand, and of bone ma...
International audienceThe precise diagnosis of an immunodeficiency is sometimes difficult to assess,...
The elucidation of the genes leading to selected immune defects has acceler-ated our understanding o...
Review on Bruton's agammaglobulinemia, with data on clinics, and the genes involved
The study of human T-cell PIDs with Mendelian inheritance has enabled the molecular characterization...
Primary immunodeficiency disorders are a recognized public health problem worldwide. The prototype o...
X-linked agammaglobulinemia (XLA) is a rare genetic disease caused by a mutation in the Bruton tyros...
The X chromosome-linked antibody deficiency disease, X-linked agammaglobulinemia (XLA), results from...
The identification of a cytoplasmic tyrosine kinase, Btk, as the defective protein in human XLA and ...
Mutation pattern was characterized in the Bruton's tyrosine kinase gene (BTK) in 26 patients with X-...
Introduction: X-linked agammaglobulinemia (XLA) is the most common primary immunodeficiency in man, ...
Genetic testing has become important in the repertoire for the diagnosis of primary immunodeficienci...
Primary antibody deficiencies represent the most frequent genetic diseases of the immune system and ...
More than 50 years after Ogdeon Bruton's discovery of congenital agammaglobulinemia, human primary i...
La agammaglobulinemia ligada al X o de Bruton constituye el prototipo de deficiencia primaria de cél...
In the last fifteen years, therapeutic use of intravenous immunoglobulin on one hand, and of bone ma...
International audienceThe precise diagnosis of an immunodeficiency is sometimes difficult to assess,...
The elucidation of the genes leading to selected immune defects has acceler-ated our understanding o...
Review on Bruton's agammaglobulinemia, with data on clinics, and the genes involved
The study of human T-cell PIDs with Mendelian inheritance has enabled the molecular characterization...
Primary immunodeficiency disorders are a recognized public health problem worldwide. The prototype o...
X-linked agammaglobulinemia (XLA) is a rare genetic disease caused by a mutation in the Bruton tyros...
The X chromosome-linked antibody deficiency disease, X-linked agammaglobulinemia (XLA), results from...
The identification of a cytoplasmic tyrosine kinase, Btk, as the defective protein in human XLA and ...
Mutation pattern was characterized in the Bruton's tyrosine kinase gene (BTK) in 26 patients with X-...
Introduction: X-linked agammaglobulinemia (XLA) is the most common primary immunodeficiency in man, ...
Genetic testing has become important in the repertoire for the diagnosis of primary immunodeficienci...