Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Devanshi Mehta"'
Autor:
Akshit Chitkara, Nirmaljot Kaur, Aditya Desai, Devanshi Mehta, Fnu Anamika, Srawani Sarkar, Nandini Gowda, Prabhdeep Sethi, Rajat Thawani, Emerson Y. Chen
Publikováno v:
Cancer Medicine, Vol 12, Iss 24, Pp 21579-21591 (2023)
Abstract Background Guidelines show that for metastatic colorectal cancer (mCRC), a combination of three‐drug regimens, fluorouracil, leucovorin, and oxaliplatin and bevacizumab (BVZ), is one of the first‐line standard therapies. BVZ is generally
Externí odkaz:
https://doaj.org/article/5e4514c1cdef4a6a99e4646b5cda7162
Autor:
Zoe S. Gan, Sherman C. Stein, Randel Swanson, Shaobo Guan, Lizette Garcia, Devanshi Mehta, Douglas H. Smith
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Blood biomarkers have been explored for their potential to provide objective measures in the assessment of traumatic brain injury (TBI). However, it is not clear which biomarkers are best for diagnosis and prognosis in different severities of TBI. He
Externí odkaz:
https://doaj.org/article/321ae1822ab14374b5a236d7ea70221e
Publikováno v:
Advances in Human Biology, Vol 6, Iss 1, Pp 61-64 (2016)
Background: Ectodermal dysplasia is a hereditary group of disorders which are manifested as X-linked recessive trait and has a full expression in males, whereas females show little or no signs of the disorder. This disorder leads to disturbances in t
Externí odkaz:
https://doaj.org/article/98ef807863354ccfbee8a00759451550
Publikováno v:
The Clinical Respiratory Journal. 15:728-734
INTRODUCTION Rural regions have unique challenges with the implementation of new therapies upon discharge from the hospital due to multiple barriers. OBJECTIVES We investigated the effect of home non-invasive ventilation (NIV) plus the implementation
Autor:
Aditya Desai, Akshit Chitkara, Devanshi Mehta, Nirmaljot Kaur, Darshi Desai, FNU Anamika, Nandini Gowda, Prabhdeep S. Sethi, Padmini Varadarajan, Ramdas Pai
Publikováno v:
Journal of the American College of Cardiology. 81:2313
Autor:
Aditya Desai, Darshi Desai, Arnold Gan, Devanshi Mehta, Kimberly R. Ding, Francis Gan, Prabhdeep S. Sethi, Ashis Mukherjee, Ramdas Pai, Narut Prasitlumkum
Publikováno v:
Journal of the American College of Cardiology. 81:954
Autor:
Jenna A. Moran, John A. Branda, Sarah P. Hammond, Lyn M. Duncan, Julian A. Villalba, Nathan P. Wiederhold, Amir T. Fathi, Steven T. Chen, Devanshi Mehta, Connie Cañete-Gibas, Samuel A Hofacker, Jessica Cervantes
Publikováno v:
Open Forum Infectious Diseases
Certain Penicillium species are emerging opportunistic pathogens. While these can be common causes of airborne contamination of clinical cultures, an increasing number of reports describe clinically significant disease in the immunocompromised popula
Autor:
Alexander Kettering, Reza Hessabi, William Ryan, Christiaan A Rees, Julia L. Berkowitz, Devanshi Mehta, Bianca Di Cocco, Sofia Rodriguez, Kimberly A. Gifford
Publikováno v:
Academic Medicine. 96:s183-S184
Autor:
Blake D. Hansen, Sylvia A. Huisman, Lynne M. Kerr, Ian D. Krantz, Matthew A. Deardorff, Jason A. Mills, Alena Egense, Jeremy Morgan, Meng Wu, Dale Dorsett, Devanshi Mehta, Olivia L. Katz, Katsuhiko Shirahige, Sarah E. Noon, Chiara Bettale, Pamela S. Herrera, Richard E. Haaland, Joseph P. McCleery, Antonie D. Kline, Cheri S. Carrico, Jo Moss, Siddharth Srivastava, Emily Taylor-Snell, Jennifer L. Gerton, Marco A. Grados, Antonio Musio, Anne L. Calof, Julia A. Horsfield
Publikováno v:
American journal of medical genetics. Part A, 173(5), 1172-1185. Wiley-Liss Inc.
Cornelia de Lange Syndrome (CdLS) is due to mutations in the genes for the structural and regulatory proteins that make up the cohesin complex, and is considered a cohesinopathy disorder or, more recently, a transcriptomopathy. New phenotypes have be
Autor:
Julian L. Allen, Ian D. Krantz, Joseph Piccione, Xueqin Zhang, Nobuhiko Okamoto, Chiara Bettale, Xiyu He, Naomichi Matsumoto, Xiaoqing Shi, Aimei Lu, Devanshi Mehta, Noriko Miyake, E. Haan, Honglin Wu, Sarah E. Raible, Susan M. White, Maninder Kaur, Kosuke Izumi, Qingjie Zhao, Sarah K. Fiordaliso, Kristina Cusmano-Ozog, Livija Medne, Yiran Guo, Qi Lei, Marlène Rio, Eriko Nishi, Mary E. Pipan
Publikováno v:
American Journal of Medical Genetics Part A.
CHOPS syndrome is a multisystem disorder caused by missense mutations in AFF4. Previously, we reported three individuals whose primary phenotype included cognitive impairment and coarse facies, heart defects, obesity, pulmonary involvement, and short