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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 ...
Arye Rubinstein, B Speck, M Jeannet
exaly +4 more sources
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.
R, 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 N, Schimke +2 more
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The immunologic deficiency of Rubinstein-Taybi syndrome
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.
F. Wertheimer +5 more
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[Primary immunologic deficiency syndromes in man].
Arkhiv patologii, 1977Current concepts on the immune system, the genesis of human T- and B-lymphocytes, and their functional properties are presented as well as current data on the pathogenesis and classification of hereditary defects of the human immune system. The main forms of immunity deficiency conditions are described.
, Lopukhin YuM +2 more
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[General variable immunologic deficiency with malabsorption syndrome].
Klinicheskaia meditsina, 1990Twenty-two patients with general variable immunodeficiency (GVI) and malabsorption syndrome (MS) were followed up for 2-12 years. III degree MS was found in 17 cases. Serum immunoglobulins concentration and T-lymphocyte count were reduced, the latter at the expense of theophylline-resistant and active E-RFC. With casein and milk albumin as the antigens,
A I, Parfenov +3 more
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Current and potential new treatment strategies for creatine deficiency syndromes
Molecular Genetics and Metabolism, 2022Olivier Braissant
exaly
Immunologic Alterations in Acquired Immune Deficiency Syndrome
2015M S, Gottlieb, J L, Fahey
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