Results 201 to 210 of about 12,870 (263)
Clinical and genetic features of UNC13D deficiency with hypogammaglobulinemia. [PDF]
Front ImmunolXiong L +8 more
europepmc +1 more source
Bloodless Surgeries in Pediatric Dentistry: A Review.
J Pharm Bioallied SciAggarwal N +4 more
europepmc +1 more source
X-linked Agammaglobulinemia [PDF]
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
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International Journal of Biological Macromolecules, 2020
Taj Mohammad, Mohd Amir, Kartikay Prasad
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Taj Mohammad, Mohd Amir, Kartikay Prasad
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Agammaglobulinemia in the adult [PDF]
The American Journal of Medicine, 1955 Abstract Two case studies of adult white men with agammaglobulinemia and splenomegaly are reported. One has been subject to repeated bacterial infections of the skin and respiratory tract and has had several attacks of severe diarrhea. The other patient has had recurrent small bowel obstruction probably due to inflammatory lymph node enlargement, but ...
Marvin Rosecan +2 more
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Medical Clinics of North America, 1956
Although a diminution of serum gamma globulin or even its total absence electrophoretically not infrequently follows an infection in early childhood, it is much less common in adults. A persistent diminution or absence of serum gamma globulin as the cause of multiple infections is a concept that was introduced by Bruton 1 in 1952.
Harry F. Wechsler, M. Joel Wolf
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Although a diminution of serum gamma globulin or even its total absence electrophoretically not infrequently follows an infection in early childhood, it is much less common in adults. A persistent diminution or absence of serum gamma globulin as the cause of multiple infections is a concept that was introduced by Bruton 1 in 1952.
Harry F. Wechsler, M. Joel Wolf
openaire +5 more sources
Eosinophilia and Agammaglobulinemia
Pediatrics, 1965While studying a group of children with the visceral larva migrans syndrome we encountered in the patient group a child with agammaglobulinemia. This child, in spite of an almost complete absence of immune globulins, exhibited the massive eosinophilia characteristic of the tissue phase of helminth infections. Case Report L.
Carolyn C. Huntley, Margarita C. Costas
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Annals of Internal Medicine, 1957
Excerpt The purpose of this report is to call attention to another case of agammaglobulinemia in an adult, to emphasize a few of the features of this interesting process, and to add to the accumula...
J. W. Savacool, Ray P. Landes
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Excerpt The purpose of this report is to call attention to another case of agammaglobulinemia in an adult, to emphasize a few of the features of this interesting process, and to add to the accumula...
J. W. Savacool, Ray P. Landes
openaire +3 more sources
Journal of the American Veterinary Medical Association, 1979
SUMMARY Immunologic deficiency was suspected in an 18-month-old Standardbred horse with persistent fever, multifocal bacterial infection, and neutropenia with a large number of immature neutrophils. Serum protein electrophoresis revealed marked depression of the gamma-globulin fraction (0.2 g/100 ml).
D A, Deem +3 more
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SUMMARY Immunologic deficiency was suspected in an 18-month-old Standardbred horse with persistent fever, multifocal bacterial infection, and neutropenia with a large number of immature neutrophils. Serum protein electrophoresis revealed marked depression of the gamma-globulin fraction (0.2 g/100 ml).
D A, Deem +3 more
openaire +2 more sources