Salmonella and Campylobacter infections occur commonly in children. Some of these
infections are severe, requiring treatment with antimicrobial agents. Many classes of …

Wolfram syndrome (WS) is the inherited association of juvenile‐onset insulin‐dependant
diabetes mellitus and progressive bilateral optic atrophy. A nuclear gene, WFS1/wolframin …

Salmonella resistant to extended-spectrum cephalosporins (ESCs) have emerged
worldwide since 1988. By 2004, 43 countries had reported this public health problem …

Standardized rapid pulsed-field gel electrophoresis (PFGE) protocols for the subtyping of
Escherichia coli O157: H7, Salmonella serotypes, and Shigella species are described …

PulseNet, the national molecular subtyping network for foodborne disease surveillance, was
established by the Centers for Disease Control and Prevention and several state health …

Objective.—Esherichia coliO157: H7 causes hemorrhagic colitis and the hemolytic uremic
syndrome. In the fall of 1991, an outbreak ofE coliO157: H7 infections in southeastern …

Abstract Background A once-weekly, 2.4-mg dose of subcutaneous semaglutide, a glucagon-
like peptide-1 receptor agonist, is used to treat obesity in adults, but assessment of the drug …

Objective.—To determine the source of and describe a large outbreak ofEscherichia
coliO157: H7 infections in Washington State. Design.—Case-control study; environmental …

Wolcott-Rallison syndrome (WRS) is a rare, autosomal recessive disorder characterized by
permanent neonatal or early infancy insulin-dependent diabetes. Epiphyseal dysplasia …

Summary Monocarboxylate transporter 8 (MCT8) is a thyroid hormone transporter, the gene
of which is located on the X chromosome. We tested whether mutations in MCT8 cause …