Results 151 to 160 of about 142,171 (218)

Case Report: Profound newborn leukopenia related to a novel RAC2 variant. [PDF]

open access: yesFront Pediatr
Hall G   +10 more
europepmc   +1 more source

Genetic Variants in Early-Onset Inflammatory Bowel Disease: Monogenic Causes and Clinical Implications. [PDF]

open access: yesChildren (Basel)
Demirtas Guner D   +11 more
europepmc   +1 more source

Acquired immune deficiency syndromes: A review of immunologic aspects

Clinical Immunology Newsletter, 1983
John L. Fahey   +2 more
openaire   +3 more sources

Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept.

European Journal of Gastroenterology and Hepathology, 2021
Gut involvement is frequent in immunologic disorders, especially with inflammatory manifestations but also with cancer. In the last years, advances in functional and genetic testing have improved the diagnostic and therapeutic approach to immune ...
G. Angelino   +23 more
semanticscholar   +1 more source

Virologic and immunologic characterization of symptomatic and asymptomatic primary HIV-1 infection.

Journal of Acquired Immune Deficiency Syndromes & Human Retrovirology, 1995
To define virologic and immunologic differences in patients with acute symptomatic and asymptomatic primary human immunodeficiency virus type 1 (HIV-1) infection, sequential plasma specimens were obtained longitudinally for 1-2 years postseroconversion ...
D. Henrard   +6 more
semanticscholar   +1 more source

Acquired Immuno-Deficiency Syndrome: Epidemiology, Virology, and Immunology

Annual Review of Medicine, 1985
Acquired immunodeficiency syndrome indicates opportunistic infection or unusual malignancy associated with a marked deficiency of cell mediated immunity in the absence of any other cause of the immune defect. This review examines epidemiology, virology, and immunology associated with this disorder.
Harry Hollander   +2 more
openaire   +3 more sources

Clinical, Immunological and Histopathological Evidence for Thymic Deficiency in Down’s Syndrome (Mongolism)

1976
Down’s syndrome (DS) is a chromosomal disorder leading to genetic malformations of various systems, the most marked giving rise to mental retardation and skeletal and heart abnormalities. The incidence of this disorder ranges from 1 per 1000 births in young mothers, to 1 per 50 births in mothers over 40 years of age.
Handzel Zt   +6 more
openaire   +3 more sources

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