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combined immunodeficiency disease

CABI Compendium, 2022
This datasheet on combined immunodeficiency disease covers Identity, Hosts/Species Affected.

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Defining combined immunodeficiency

Journal of Allergy and Clinical Immunology, 2012
Although the extreme condition of typical profound T-cell dysfunction (TD), severe combined immunodeficiency (SCID), has been carefully defined, we are currently in the process of better defining less typical T-cell deficiencies, which tend to present with autologous circulating T-cell combined immunodeficiency (CID).
Chaim M, Roifman, Raz, Somech, Fotini, Kavadas, Linda, Pires, Amit, Nahum, Ilan, Dalal, Eyal, Grunebaum   +6 more
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Severe Combined Immunodeficiency Disorders

Immunology and Allergy Clinics of North America, 2015
Severe combined immunodeficiency disorders represent pediatric emergencies due to absence of adaptive immune responses to infections. The conditions result from either intrinsic defects in T-cell development (ie, severe combined immunodeficiency disease [SCID]) or congenital athymia (eg, complete DiGeorge anomaly).
Ivan K, Chinn, William T, Shearer
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Severe Combined Immunodeficiency Diseases

Springer Seminars in Immunopathology, 1978
The most severe, and also a relatively common immunodeficiency syndrome involves both antibody- and cell-mediated immune mechanisms. In more modern terms the ‘severe combined immunodeficiency’ syndromes (SCID) are defined as all diseases resulting from marked and longlasting functional impairment of both the T- and B-cell system.
W. H. Hitzig, L. J. Dooren, J. M. Vossen
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Keeping it in the family: the case for considering late-onset combined immunodeficiency a subset of common variable immunodeficiency disorders

Expert Review of Clinical Immunology, 2018
Introduction: Common variable immunodeficiency disorders (CVID) are the most frequent symptomatic primary immune defect in adults. Within the broad spectrum of CVID, a proportion of patients present with a predominant T cell phenotype associated with ...
R. Ameratunga, Y. Ahn, A. Jordan, K. Lehnert, S. Brothers, S. Woon   +5 more
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Combined immunodeficiency in a calf

Journal of the American Veterinary Medical Association, 1989
Combined immunodeficiency was documented in a 6-week-old Angus calf. The calf had lymphopenia, undetectable serum IgM or IgA, and low concentrations of serum IgG (420 mg/dl). The calf was treated for diarrhea, pneumonia, and shock, and was given antimicrobial drugs, fluids, and plasma.
P A, Bartram, B P, Smith, C, Holmberg, C P, Mandell   +3 more
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Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease.

Science, 2000
M. Cavazzana‐Calvo, S. Hacein‐Bey, G. Basile, F. Gross, E. Yvon, P. Nusbaum, F. Selz, C. Hue, S. Certain, J. Casanova, P. Bousso, F. Deist, A. Fischer   +12 more
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X-linked severe combined immunodeficiency

Clinical Immunology and Immunopathology, 1991
Between a third and half of all males with SCID and no family history of immunodeficiency represent the first manifestation in their family of a new mutation of the gene that causes X-linked SCID. These patients, like boys with a positive family history of X-linked SCID, have markedly reduced numbers of T cells, elevated numbers of B cells, and ...
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A20 Haploinsufficiency Presenting with a Combined Immunodeficiency

Journal of Clinical Immunology, 2020
M. Gans, Hongying Wang, N. S. Moura, I. Aksentijevich, A. Rubinstein   +4 more
semanticscholar   +1 more source