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LAD1 is a redirect to Ladinin 1

searching for LAD1 5 found (8 total)

alternate case: lAD1

Leukocyte adhesion deficiency-1 (331 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. The main sign of the disease is life-threatening, recurrent
Leukocyte adhesion deficiency (795 words) [view diff] exact match in snippet view article find links to article
of leukocyte adhesion deficiency include LAD1, LAD2, and LAD3. LAD1 is the most common. Patients with LAD1 have an inherited molecular defect that causes
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
Lymphocyte function-associated antigen 1 (959 words) [view diff] exact match in snippet view article find links to article
functioning neutrophils. LAD1, a subtype of LAD, is caused by a lack of integrins that contain the beta subunit, including LFA-1. LAD1 is characterized by
Outline of immunology (2,641 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: