Results 141 to 150 of about 10,731 (180)

Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects

open access: yesExpert Review of Clinical Immunology, 2016
OBJECTIVES: Impairment in early B-cell development can cause a predominantly antibody deficiency with severe depletion of peripheral B-cells. Mutations in the gene encoding for Bruton's-tyrosine-kinase (BTK) and the components of the pre-B-cell ...
Seyed Alireza Mahdaviani   +2 more
exaly   +2 more sources

Agammaglobulinemia in the adult

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 ...
M, ROSECAN, F E, TROBAUGH, W H, DANFORTH
openaire   +2 more sources

Agammaglobulinemia in a Horse

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
openaire   +2 more sources

AGAMMAGLOBULINEMIA IN ADULTS

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, R P, LANDES
openaire   +2 more sources

Eosinophilia and Agammaglobulinemia

Pediatrics, 1965
While 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.
C C, Huntley, M C, Costas
openaire   +2 more sources

Comparison of clinical and immunological features and mortality in common variable immunodeficiency and agammaglobulinemia patients

open access: yesImmunology Letters, 2019
Common Variable Immunodeficiency (CVID)and agammaglobulinemia are two of the main types of symptomatic primary antibody deficiencies. The pathogenic origins of these two diseases are different; agammaglobulinemia is a group of inherited disorders that ...
Gholamreza Azizi, Majid Khoshmirsafa
exaly   +1 more source

AGAMMAGLOBULINEMIA

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 decade with agammaglobulinemia

The Journal of Pediatrics, 1962
Summary This progress report is presented a decade after recognition of a patient with agammaglobulinemia. It includes a brief description and follow-up of the first recognized patient, a brief summary of significant advances in the elucidation of agammaglobulinemia as a disease entity, and some predictions on the type of advances which may be made ...
openaire   +2 more sources

AGAMMAGLOBULINEMIA

Annals of Internal Medicine, 1954
A S, PRASAD, D W, KOZA
openaire   +4 more sources

ADULT AGAMMAGLOBULINEMIA

Archives of Internal Medicine, 1955
R L, WALL, S, SASLAW
openaire   +2 more sources

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