Results 1 to 10 of about 50 (46)
The immunological and infectious sequelae of the acquired immune deficiency syndrome. [PDF]
The Journal of experimental medicine, 1988 In spite of much ongoing experimentation, the consensus view is that a vaccine will be difficult to achieve. New strategies of chemo- and immunotherapy may bear more rapid results.
Cohn, Zanvil A., Steinman, Ralph M.
openaire +3 more sources
Immunological Deficiency Syndromes [Abridged] [PDF]
Proceedings of the Royal Society of Medicine, 1968 +16 more sources
Immunological profile in a chromosome 18 deletion syndrome with IgA deficiency. [PDF]
Journal of Medical Genetics, 1969 I A Uchida +5 more
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Some of the next articles are maybe not open access.
IMMUNOLOGICAL RESTITUTION IN LYMPHOPENIC IMMUNOLOGICAL DEFICIENCY SYNDROME
The Lancet, 1968Abstract All previous attempts at restoring immunological capacity in cases of the lymphopenic (Swiss type) immunological deficiency syndrome have failed. An 8-month-old boy with this syndrome and oral moniliasis was given maternal blood and foetal thymus and liver cells.
Richard Hong +5 more
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Immunologic Deficiency in the Congenital Rubella Syndrome
Archives of Pediatrics & Adolescent Medicine, 1969RECENT observations have indicated that disorders of the immune system must be added to the spectrum of congenital anomalies that are associated with prenatal infection by the rubella virus. Impaired responses of blood lymphocytes to mitogens1and antigens,2depressed delayed cutaneous hypersensitivity,2and abnormal concentrations of serum ...
R. Neil Schimke +2 more
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The immunologic deficiency of Rubinstein-Taybi syndrome*1
Journal of Allergy and Clinical Immunology, 2004Abstract Rationale Rubinstein-Tabyi syndrome is characterized by broad toes and thumbs. It is estimated that approximately 75% of patient with RTS experience respiratory infections. We have found that an immunologic abnormality may be the true cause of their infections.
Jack Rubinstein +5 more
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Successful Bone-Marrow Transplantation in a Lymphopenic Immunologic Deficiency Syndrome
New England Journal of Medicine, 1971Abstract A 12-year-old boy with lymphopenic immunologic deficiency syndrome (common variable type) was treated with an infusion of bone-marrow cells from a 10-year-old HL-A identical brother. Despite the HL-A identity and a negative mixed lymphocyte culture, a severe graft-versus-host reaction developed from which he recovered, except for persisting ...
M. Jeannet, B. Speck, A. Rubinstein
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Archives of Dermatology, 1973
A new familial heredodegenerative disorder with pancytopenia, immunologic deficiency, and cutaneous malignancies is reported. One patient had a prolonged course of multiple pneumothoraces, infections, and cutaneous malignancies. His immunologic abnormalities included near absence of IgA, elevated IgG with later development of abnormal γ-globulin, and ...
David Abels, William B. Reed
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A new familial heredodegenerative disorder with pancytopenia, immunologic deficiency, and cutaneous malignancies is reported. One patient had a prolonged course of multiple pneumothoraces, infections, and cutaneous malignancies. His immunologic abnormalities included near absence of IgA, elevated IgG with later development of abnormal γ-globulin, and ...
David Abels, William B. Reed
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Immunological Deficiency in the Down Syndrome: Importance of the Age Factor
1979Many observations have pointed out an immunological deficiency in Down syndrome. Such deficiency concerns both the B cells system and the T cells system. Most of such studies have been done on infants or very young subjects.
V. Argentiero, B. Tavolato
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