• A new leukocyte hyperadhesion syndrome of delayed cord separation, skin infection, and nephrosis
• A novel form of integrin dysfunction involving beta1, beta2, and beta3 integrins
• An integrated, functionally annotated gene map of the DXS8026-ELK1 interval on human Xp11.3-Xp11.23: potential hotspot for neurogenetic disorders
• DecodeME: community recruitment for a large genetics study of myalgic encephalomyelitis / chronic fatigue syndrome
• Functional and structural studies of wild type SOX9 and mutations causing campomelic dysplasia
• How T cells use LFA-1 to attach and migrate
• Is the History of Erectile Dysfunction a Reliable Risk Factor for New Onset Acute Myocardial Infarction? A Systematic Review and Meta-Analysis
• Leukocyte adhesion deficiency-III in an African-American patient
• Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation
• Mechanisms contributing to the activity of integrins on leukocytes
• Prevalence and genotype of Mycoplasma bovis in beef cattle after arrival at a feedlot
• Sleep Disordered Breathing and Academic Performance: A Meta-analysis
• Surviving campomelic dysplasia has the radiological features of the previously reported ischio-pubic-patella syndrome
• Two mutations in the KINDLIN3 gene of a new leukocyte adhesion deficiency III patient reveal distinct effects on leukocyte function in vitro
• Typing myalgic encephalomyelitis by infection at onset: A DecodeME study