Results 171 to 180 of about 19,116 (219)

A Novel Pathogenic Variant in TRAC Gene Associated with SCID Phenotype: Expanding the Genetic and Clinical Spectrum. [PDF]

open access: yesJ Clin Immunol
Karaselek MA   +15 more
europepmc   +1 more source
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Cellular radiosensitivity in human severe-combined-immunodeficiency (SCID) syndromes

Radiotherapy and Oncology, 1997
The aim of the work was to establish to what extent a variety of human severe-combined-immunodeficiency (SCID) disorders are associated with in vitro cellular hypersensitivity to ionizing radiation.A study was made of fibroblast strains established from individuals with adenosine deaminase deficiency, T(-)B(-) SCID, Omenn's syndrome and a SCID ...
West Cm, Jolyon H Hendry, J H Hendry
exaly   +3 more sources

Malakoplakia of the Colon in an Infant with Severe Combined Immunodeficiency (SCID) and Charge Association

Pathology Research and Practice, 2000
We report on malakoplakia of the colon observed in a six month old girl in a setting of severe combined immunodeficiency (SCID) and a malformational syndrome termed CHARGE association. By the age of six months, hemorrhagic diarrhea had developed, and multiple ulcers were seen at colonoscopy.
Michael O Kurrer, Bernhard Stamm
exaly   +4 more sources

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