Results 241 to 250 of about 18,093 (282)
Some of the next articles are maybe not open access.
Indian Journal of Pediatrics, 2016
X-linked agammaglobulinemia (XLA) is one of the commonest primary immune deficiencies encountered in pediatric clinical practice. In adults, common variable immunodeficiency (CVID) is the most common primary immunodeficiency disease (PID). It is an X-linked disorder characterized by increased susceptibility to encapsulated bacteria, severe ...
Deepti Suri, Amit Rawat, Surjit Singh
exaly +3 more sources
X-linked agammaglobulinemia (XLA) is one of the commonest primary immune deficiencies encountered in pediatric clinical practice. In adults, common variable immunodeficiency (CVID) is the most common primary immunodeficiency disease (PID). It is an X-linked disorder characterized by increased susceptibility to encapsulated bacteria, severe ...
Deepti Suri, Amit Rawat, Surjit Singh
exaly +3 more sources
International Journal of Biological Macromolecules, 2020
Taj Mohammad, Mohd Amir, Kartikay Prasad
exaly +2 more sources
Taj Mohammad, Mohd Amir, Kartikay Prasad
exaly +2 more sources
Autosomal Recessive Agammaglobulinemia Due to a Homozygous Mutation in PIK3R1
Journal of Clinical Immunology, 2017Julia E M Upton
exaly +2 more sources
Journal of Medical Virology
Immunocompromised individuals are at significantly elevated risk for severe courses of coronavirus disease 2019 (COVID‐19). In addition to vaccination, severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) neutralizing antibodies (nAbs) have been ...
M. Karbiener +8 more
semanticscholar +1 more source
Immunocompromised individuals are at significantly elevated risk for severe courses of coronavirus disease 2019 (COVID‐19). In addition to vaccination, severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) neutralizing antibodies (nAbs) have been ...
M. Karbiener +8 more
semanticscholar +1 more source
Pediatrics, 1952
A hitherto unrecognized entity manifested by complete absence of gamma globulin with otherwise normal serum proteins and recurrent pneumococcal sepsis is described in an 8 year old male. The patient appears to be normal in other respects and after extensive study no structural or functional change could be demonstrated in any body system although gamma
openaire +2 more sources
A hitherto unrecognized entity manifested by complete absence of gamma globulin with otherwise normal serum proteins and recurrent pneumococcal sepsis is described in an 8 year old male. The patient appears to be normal in other respects and after extensive study no structural or functional change could be demonstrated in any body system although gamma
openaire +2 more sources
Pediatric Allergy and Immunology, 2020
Congenital agammaglobulinemia is the first primary immunodeficiency disorder characterized by a defect in B lymphocyte development and subsequently decreased immunoglobulin levels.
Saba Fekrvand +22 more
semanticscholar +1 more source
Congenital agammaglobulinemia is the first primary immunodeficiency disorder characterized by a defect in B lymphocyte development and subsequently decreased immunoglobulin levels.
Saba Fekrvand +22 more
semanticscholar +1 more source