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searching for LAD1 4 found (6 total)

alternate case: lAD1

Leukocyte adhesion deficiency-1 (325 words) [view diff] exact match in snippet view article find links to article

Leukocyte adhesion deficiency-1 (LAD1) is a rare and often fatal genetic disorder in humans. LAD1 is caused by mutations in the ITGB2 gene which are
Leukocyte adhesion deficiency (724 words) [view diff] exact match in snippet view article find links to article
resulting in recurrent infections. LAD is currently divided into three subtypes: LAD1, LAD2, and the recently described LAD3, also known as LAD-1/variant. In LAD3
Congenital disorder of glycosylation type IIc (405 words) [view diff] exact match in snippet view article find links to article
in patients with LAD1, including pneumonia, peridontitis, otitis media, and localized cellulitis. Similar to that in patients with LAD1, their infections
Outline of immunology (2,749 words) [view diff] exact match in snippet view article find links to article
chemotaxis/degranulation: Leukocyte adhesion deficiency LAD1 LAD2 Chédiak–Higashi syndrome Neutrophil-specific granule deficiency respiratory burst: