Results 241 to 250 of about 18,379 (288)
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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
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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
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Médecine et maladies infectieuses, 2020
BACKGROUND Campylobacter is the most common cause of infectious diarrhea in agammaglobulinemia patients. These infections can be severe, prolonged, and recurrent in such patients.
M. Dan, M. Parizade
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BACKGROUND Campylobacter is the most common cause of infectious diarrhea in agammaglobulinemia patients. These infections can be severe, prolonged, and recurrent in such patients.
M. Dan, M. Parizade
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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
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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
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Autosomal Recessive Agammaglobulinemia - first case with a novel TCF3 mutation from Pakistan.
Clinical Immunology, 2019Autosomal Recessive Agammaglobulinemia (ARA) is an uncommon type of primary immunodeficiency characterized by mutations in genes responsible for early B cell differentiation and function.
S. Qureshi, M. Sheikh, F. Qamar
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Immunology 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 ...
Y. Bagheri +11 more
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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 ...
Y. Bagheri +11 more
semanticscholar +1 more source
The 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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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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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.
C C, Huntley, M C, Costas
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