Zobrazeno 1 - 10
of 59
pro vyhledávání: '"John F. Bastian"'
Autor:
James L. Mueller, Lori Broderick, Hal M. Hoffman, Christopher D. Putnam, Chhavi Gandhi, Karin S. Peterson, Seema S. Aceves, Patricia C. Giclas, Katayoon Shayan, Robert O. Newbury, Bradley M. Peterson, John F. Bastian, Robert Sheets
Publikováno v:
Journal of Clinical Immunology. 33:162-171
Acute Hemorrhagic Leukoencephalitis (AHLE) is a rare demyelinating disorder of acute onset, rapid deterioration and significant morbidity and mortality. Most often described as a post-infectious complication of an upper respiratory illness, its preci
Autor:
David H. Broide, Seema S. Aceves, Hal M. Hoffman, Ranjan Dohil, John F. Bastian, Diana Chen, Robert O. Newbury, James L. Mueller
Publikováno v:
Allergy. 65:109-116
Eosinophilic esophagitis (EE) is a disease of increasing prevalence and is diagnosed if esophageal histology demonstrates >15 epithelial eosinophils per high power field (hpf), especially in the context of acid blockade to exclude gastroesophageal re
Publikováno v:
Annals of Allergy, Asthma & Immunology. 103:401-406
Eosinophilic esophagitis (EE) is an increasingly recognized allergic disease entity that is difficult to distinguish clinically from other causes of esophagitis, especially gastroesophageal reflux disease (GERD). To our knowledge, there are no prospe
Publikováno v:
Pediatric Infectious Disease Journal. 27:377-383
Kawasaki syndrome (KS) is the most common cause of acquired pediatric heart disease in the developed world. There have been 2 distinctive patterns for the emergence of KS that are likely related to several factors including exposure to the causative
Publikováno v:
Journal of Clinical Gastroenterology. 41:252-256
To determine the clinical, endoscopic, and histologic criteria that distinguish children with eosinophilic esophagitis (EE) from those with non-EE diagnoses.EE is a disease of escalating incidence. Distinguishing children with EE from those with non-
Autor:
Christena L. Turner, John F. Bastian, Jane C. Burns, Lawrence A. Palinkas, Annie S. Kao, Matthew S. Wilder
Publikováno v:
Pediatric Infectious Disease Journal. 26:256-260
Despite the availability of an effective treatment of Kawasaki syndrome, children continue to develop preventable morbidity and mortality from complications of this acute vasculitis. Kawasaki syndrome resolves spontaneously, but coronary aneurysms oc
Autor:
Joshua Fierer, George Y. Liu, Vivekanand Datta, Hal M. Hoffman, John T. Buchanan, Victor Nizet, John F. Bastian, Anthony Essex
Publikováno v:
The Journal of Experimental Medicine
Golden color imparted by carotenoid pigments is the eponymous feature of the human pathogen Staphylococcus aureus. Here we demonstrate a role of this hallmark phenotype in virulence. Compared with the wild-type (WT) bacterium, a S. aureus mutant with
Publikováno v:
Progress in Pediatric Cardiology. 19:91-97
This paper describes the historical evolution of the Kawasaki disease (KD) from a pediatric vasculitis to a clinical syndrome with a putative infectious cause. The KD clinical criteria were developed before the general acceptance of coronary artery a
Publikováno v:
Bulletin of the History of Medicine. 78:410-439
Kawasaki disease is a rash/fever illness of early childhood in which coronary artery aneurysms (CAA), sometimes fatal, may develop in up to 25 percent of untreated children. Because its etiology and pathophysiology are unknown and no diagnostic labor
Publikováno v:
Perspectives in Biology and Medicine. 46:216-233
This paper describes the historical evolution of the Kawasaki disease (KD) case definition and its limitations for identification and treatment of children at risk for coronary artery aneurysms (CAA). The dominant view of pathogenesis is that an unkn