Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ariel Karten"'
Autor:
Diana S. Wolfe, Christina Liu, Jack Alboucai, Ariel Karten, Juliet Mushi, Shira Yellin, Julia L. Berkowitz, Shayna Vega, Nicole Felix, Wasla Liaqat, Rohan Kankaria, Thammatat Vorawandthanachai, Anna E. Bortnick
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 8, p 250 (2022)
Peripartum cardiomyopathy (PPCM) is idiopathic systolic congestive heart failure around pregnancy. Comparisons with matched controls are lacking. We investigated maternal characteristics and outcomes up to 12 months in a cohort admitted to Montefiore
Externí odkaz:
https://doaj.org/article/49afafac00b04b3faf4f430f9a1b617d
Autor:
Allison B. Reiss, Steven E. Carsons, Lora J. Kasselman, Ariel Karten, Nicholas A. Vernice, Aaron Pinkhasov, Heather A. Renna, Joshua DeLeon, Irving H. Gomolin, Daniel S. Glass
Publikováno v:
Experimental and Molecular Pathology. 118:104604
Oxytocin (OT) is a neuropeptide hormone secreted by the posterior pituitary gland. Deficits in OT action have been observed in patients with behavioral and mood disorders, some of which correlate with an increased risk of cardiovascular disease (CVD)
Publikováno v:
Chest. 158:A675
Autor:
Faraj Kargoli, Davis Jones, Giora Weisz, Mark L. Greenberg, Michael Weinreich, Eric I. Sun, Mark Menegus, Ariel Karten, Tanush Gupta, Paul Kim, Anna E. Bortnick, Weijia Li, Ming Zhang, Azeem Latib
Publikováno v:
Journal of the American College of Cardiology. 76:B71
Publikováno v:
Chest. 158:A674
Publikováno v:
Human Molecular Genetics. 25:1690-1702
Germline mutations in the X-linked gene, methyl-CpG-binding protein 2 (MECP2), underlie most cases of Rett syndrome (RTT), an autism spectrum disorder affecting approximately one in 10 000 female live births. The disease is characterized in affected
Autor:
Jin Li, Peng Yu, Nurit Ballas, Mary F. Kritzer, Ariel Karten, Shaun Charkowick, Jialin Sun, Sivan Osenberg, Christy A. Felice, Minh Vu Chuong Nguyen
Publikováno v:
Proceedings of the National Academy of Sciences. 115
Rett syndrome (RTT) is a severe neurodevelopmental disorder that affects about 1 in 10,000 female live births. The underlying cause of RTT is mutations in the X-linked gene, methyl-CpG-binding protein 2 (MECP2); however, the molecular mechanism by wh
Publikováno v:
Brain Connectivity. 3:286-293
The lateral occipital cortex (LOC), a visual area known to be involved in object recognition, was dynamically coupled with each of two distributed patterns of neural activity depending upon the percept (default or alternative) elicited by a bistable