Zobrazeno 1 - 10
of 74
pro vyhledávání: '"William N. O'Connor"'
Autor:
Brett T. Comer, Gerhard C. Hildebrandt, William N. O'Connor, Snigdha Nutalapati, Richard O'Neal
Publikováno v:
Case Reports in Rheumatology, Vol 2021 (2021)
Case Reports in Rheumatology
Case Reports in Rheumatology
Eosinophilic angiocentric fibrosis (EAF) is an exceeding rare clinical entity and is considered a part of the spectrum of IgG4-related disease (IgG4RD). We hereby present such an unusual case of a 60-year-old female who presented to us with recurrent
Autor:
Dana L. Ionel, Fred O. Odago, Andre N. Ene, Jessica D. Lee, William N. O'Connor, Larry B. Goldstein, L. Creed Pettigrew
Publikováno v:
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 31(4)
Non-traumatic neurological deterioration is a medical emergency that may arise from diverse causes, to include cerebral infarction or intracranial hemorrhage, meningoencephalitis, seizure, hypoxic-ischemic or toxic/metabolic encephalopathy, poisoning
Autor:
Marlene E. Starr, Maria E. C. Bruno, Chenlu Ke, Allison M Owen, Dwight D. Harris, Hiroshi Saito, Beverly K Balasuriya, Phillip K. Chang, Nisha Nataraj, Victor Ortiz-Soriano, Brittany A. Zwischenberger, Arnold J. Stromberg, Javier A. Neyra, Sujata Mukherjee, William N. O'Connor
Publikováno v:
Shock
Results from preclinical sepsis studies using rodents are often criticized as not being reproducible in humans. Using a murine model, we previously reported that visceral adipose tissues (VAT) are highly active during the acute inflammatory response,
Autor:
Seth B. Gray, Andrew C. Cook, William N. O'Connor, Vi-Hue Tran, Diane E. Spicer, Robert H. Anderson, Rohit Loomba, Hieu T. Ta, Justin T. Tretter
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Background Discussions continue as to whether ventricular septal defects are best categorized according to their right ventricular geography or their borders. This is especially true when considering the perimembranous defect. Our aim, therefore, was
Publikováno v:
Transplantation proceedings. 51(9)
Fabry's disease is a X-linked hereditary disease that causes the accumulation of glycosphingolipids in tissues and organs, including the kidneys and heart. This can result in both chronic kidney disease and cardiac dysfunction, including arrhythmias
Autor:
Roberto G. Aru, Mary B. Sheppard, Akif K. Guney, William N. O'Connor, Jerald P. Wallace, Sam Tyagi, Michael C. Bounds
Publikováno v:
Annals of Vascular Surgery. 71:534.e13-534.e15
Spontaneous rupture of mesenteric vasculature associated with fibromuscular dysplasia is an unreported phenomenon. We describe a case in a 28-year-old male with a history of chronic abdominal pain who presented to our facility in hemorrhagic shock se
Publikováno v:
Echocardiography. 32:1417-1422
Infective endocarditis is a well-described cardiovascular disease that causes significant morbidity and mortality despite medical and surgical advances. Complications of endocarditis include heart failure, systemic embolization, and valvular destruct
Autor:
David H. Adams, Annapoorna Kini, Pedro R. Moreno, Meerarani Purushothaman, Prakash Krishnan, Samin K. Sharma, K-Raman Purushothaman, Anelechi C. Anyanwu, William N. O'Connor, Irene C. Turnbull
Publikováno v:
Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology. 29
Collagen cross-linking is mediated by lysyl oxidase (LOX) enzyme in the extracellular matrix (ECM) of mitral valve leaflets. Alterations in collagen content and LOX protein expression in the ECM of degenerative mitral valve may enhance leaflet expans
Autor:
Destiny F. Chau, Thomas J. Murphy, Kristopher M. Cumbermack, William N. O'Connor, Habib Srour, Lou Bezold, Deborah J. Kozik, Cristin M. Rolf, Eugene A. Hessel, Mark D. Plunkett
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 4:213-216
Congenital diaphragmatic hernia (CDH) presenting beyond the neonatal period is commonly perceived to be rare. With reported frequencies of 2.6% to 20% of all CDH, it may be an overlooked cause of mortality. Variable symptomatology makes its diagnosis
Autor:
Heidi L. Weiss, Rachel L. Stewart, William N. O'Connor, Chi Wang, Kathleen L. O'Connor, Min Chen, Tamas S Gal, Eric B. Durbin, Dava S. West
Lung cancer carries a poor prognosis and is the most common cause of cancer-related death worldwide. The integrin α6β4, a laminin receptor, promotes carcinoma progression in part by cooperating with various growth factor receptors to facilitate inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68c14c6dc036c4890e65c4cbf84f25be
https://europepmc.org/articles/PMC4938774/
https://europepmc.org/articles/PMC4938774/