Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Peter B Baker"'
Autor:
Mackenzie E. Turner, Kevin M. Blum, Tatsuya Watanabe, Erica L. Schwarz, Mahboubeh Nabavinia, Joseph T. Leland, Delaney J. Villarreal, William E. Schwartzman, Ting-Heng Chou, Peter B. Baker, Goki Matsumura, Rajesh Krishnamurthy, Andrew R. Yates, Kan N. Hor, Jay D. Humphrey, Alison L. Marsden, Mitchel R. Stacy, Toshiharu Shinoka, Christopher K. Breuer
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-10 (2024)
Abstract Advancements in congenital heart surgery have heightened the importance of durable biomaterials for adult survivors. Dystrophic calcification poses a significant risk to the long-term viability of prosthetic biomaterials in these procedures.
Externí odkaz:
https://doaj.org/article/f668f876930840c49404946d6ccd249c
Publikováno v:
Annals of Thoracic Medicine, Vol 8, Iss 4, Pp 229-230 (2013)
We present an interesting case of a complete vanishing of the left main bronchus in a lung transplant recipient who had a successful outcome due to acute respiratory support with venovenous extracorporeal membrane oxygenation in order to perform airw
Externí odkaz:
https://doaj.org/article/24c41d870b0a4ff3a9ead6810cc38472
Autor:
Eric S. Mull, Sarah Cohen, Ashish George, Katelyn Krivchenia, Stephen Druhan, Peter B. Baker, Benjamin Kopp
Although COP is idiopathic by definition, it is important to investigate each diagnosed case for potential causes, such as iatrogenic from radiation or known causative medications , connective tissue diseases, inflammatory bowel disease, malignancies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a5cb9274e1510d346529c25fde0a390
https://doi.org/10.22541/au.166028945.57549828/v1
https://doi.org/10.22541/au.166028945.57549828/v1
Publikováno v:
Pediatric Cardiology. 41:1458-1465
Mitral valve replacement (MVR) in children under 2 years is associated with significant morbidity and mortality. Decellularized porcine intestinal submucosa is a commercially available formulation of an extracellular matrix (ECM) with an indication f
Autor:
Robert J. Gajarski, Sara Fitzgerald-Butt, Ashley B. Hodge, Adam Morrison, Patrick I. McConnell, Peter B. Baker, Deipanjan Nandi
Publikováno v:
OBM Transplantation. 4:1-7
Left ventricular noncompaction cardiomyopathy (LVNC) is a rare form of heritable cardiomyopathy with wide genotypic variability, numerous phenotypic variations, and a wide spectrum of clinical disease from asymptomatic to end stage heart failure. Her
Autor:
Marc A. Levitt, Devin R. Halleran, Jeremy G. Fisher, Haley Lehmkuhl, Hira Ahmad, Richard J. Wood, Peter B. Baker
Publikováno v:
Journal of Pediatric Surgery. 55:67-70
Few data are available to substantiate the dogma commonly held by pediatric surgeons and pediatric pathologists that rectal biopsies may be inaccurate or risky in preterm neonates. We aimed to address these concerns.We performed a single-institution
Autor:
Sara N. Koenig, Elisa A. Bradley, Silvia Faravelli, Federico Forneris, Jeff Tonniges, Luigi Scietti, Holly C. Sucharski, Francesca De Giorgi, Matthew C. Bernier, Peter J. Mohler, Jordan L. Williams, Muhannad Akel, Omer Cavus, Peter B. Baker, Trevor Dew, Francesca Madiai
Publikováno v:
Transl Res
Heritable thoracic aortic disease and familial thoracic aortic aneurysm/dissection are important causes of human morbidity/mortality, most without identifiable genetic cause. In a family with familial thoracic aortic aneurysm/dissection, we identifie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b885ca028635a416f97e3bcfc95a2321
https://europepmc.org/articles/PMC8671190/
https://europepmc.org/articles/PMC8671190/
Autor:
Selene C. Koo, Vincent Magrini, Gregory L. Wheeler, Elaine R. Mardis, Kristen M. Leraas, Patrick J. Brennan, Stephanie LaHaye, Gregory Y Lauwers, Katherine E. Miller, Tracy A. Bedrosian, Anthony R. Miller, Jennifer H. Aldrink, Benjamin J. Kelly, Peter B. Baker, Peter White, Susan Colace, Kathleen M. Schieffer, Kyle Voytovich, James Fitch, Marc P. Michalsky, Bence P Kovari, Richard K. Wilson, Mark Ranalli, Sean McGrath, Catherine E. Cottrell
Publikováno v:
Genes, chromosomescancerREFERENCES. 60(9)
Gastroblastomas are rare tumors with a biphasic epithelioid/spindle cell morphology that typically present in early adulthood and have recurrent MALAT1-GLI1 fusions. We describe an adolescent patient with Wiskott-Aldrich syndrome who presented with a
Publikováno v:
Pediatric and Developmental Pathology. 22:91-97
William A (Bill) Newton Jr practiced pediatric pathology and hematology/oncology at Children’s Hospital of Columbus, Ohio, for over 40 years starting in 1952. Newton was an original member of the Pediatric Pathology Club, which preceded the Society
Publikováno v:
Journal of Surgical Case Reports
A thyroglossal duct cyst (TGDC) is a common pediatric midline neck mass. Most TGDCs occur in the region of the hyoid bone but have been found less commonly in areas from the oral cavity to the sternum. We present the first reported case of a multifoc