Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tamanna R Roshan Lal"'
Autor:
Elizabeth Roof, Cheri L Deal, Shawn E McCandless, Ronald L Cowan, Jennifer L Miller, Jill K Hamilton, Elizabeth R Roeder, Shana E McCormack, Tamanna R Roshan Lal, Hussein D Abdul-Latif, Andrea M Haqq, Kathryn S Obrynba, Laura C Torchen, Alaina P Vidmar, David H Viskochil, Jean-Pierre Chanoine, Carol K L Lam, Melinda J Pierce, Laurel L Williams, Lynne M Bird, Merlin G Butler, Diane E Jensen, Susan E Myers, Oliver J Oatman, Charumathi Baskaran, Laura J Chalmers, Cary Fu, Nathalie Alos, Scott D McLean, Ajay Shah, Barbara Y Whitman, Brent A Blumenstein, Sarah F Leonard, Jessica P Ernest, Joseph W Cormier, Sara P Cotter, Davis C Ryman
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
Context Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by endocrine and neuropsychiatric problems including hyperphagia, anxiousness, and distress. Intranasal carbetocin, an oxytocin analog, was investigated as a selective oxyto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40931114e5833e6e552c8b0c9d0399d7
https://doi.org/10.1210/clinem/dgad015
https://doi.org/10.1210/clinem/dgad015
Autor:
Natasha Shur, Andrea J. Cohen, Tamanna R. Roshan Lal, Erin MacLeod, Eyby Leon, Danielle Starin, Debra S Regier
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
In an era of increasing technology and interaction with the patient bedside, we explore the role of relocating the bedside from the hospital to the home using telemedicine. The COVID-19 pandemic pushed telemedicine from small and pilot programs to wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5935e6e301a6b0fc1190bad7ab45eaf7
https://doi.org/10.1002/ajmg.c.31882
https://doi.org/10.1002/ajmg.c.31882
Autor:
Amy S. Kimball, Antonie D. Kline, Mark A. Kliewer, Susan L Rebsamen, Julia O'Connor, Thelma Lopes, Marco A. Grados, Tamanna R. Roshan Lal, Julia L. Clemens
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 172:190-197
Neurobehavioral and developmental issues with a broad range of deficits are prominent features of Cornelia de Lange syndrome (CdLS), a disorder due to disruption of the cohesin protein complex. The etiologic relationship of these clinical findings to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b95adbe96eaa3bcff4138ff688d88c8
https://doi.org/10.1002/ajmg.c.31503
https://doi.org/10.1002/ajmg.c.31503
Autor:
Nahid Tayebi, Grisel Lopez, Tamanna R. Roshan Lal, Karin Weiss, Ginanina Monestime, Ellen Sidransky
Publikováno v:
Molecular Genetics and Metabolism. 120:S116-S117
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae668cf29b3446fe753072e87f020fa4
https://doi.org/10.1016/j.ymgme.2016.11.300
https://doi.org/10.1016/j.ymgme.2016.11.300