Zobrazeno 1 - 10
of 6 740
pro vyhledávání: '"Albright"'
Publikováno v:
Negotiation Journal. May2022, Vol. 38 Issue 2, p235-255. 21p.
Autor:
Rich, Hallie, Witteveen, April
Publikováno v:
Library Journal. Oct2023, Vol. 148 Issue 10, p12-13. 2p. 1 Color Photograph.
Autor:
ALBRIGHT, MADELEINE1
Publikováno v:
Vital Speeches of the Day. Aug2019, Vol. 85 Issue 8, p218-220. 3p.
Autor:
Joanna J. Kim, M.D., Stephanie Dufour, M.D., Sara Awad, M.B.B.S., M.H.P.E., Bryden Magee, M.D.
Publikováno v:
F&S Reports, Vol 5, Iss 4, Pp 453-457 (2024)
Objective: To report a patient with McCune-Albright syndrome (MAS) with bilateral ovarian involvement who had achieved a pregnancy through in vitro fertilization (IVF). Design: Case report. Setting: Academic fertility center. Patient(s): A 33-year-ol
Externí odkaz:
https://doaj.org/article/5246720ea616496c93ed5c52597699ba
Autor:
REILLY, KATIE (AUTHOR), Barry, Eloise (AUTHOR), Carlisle, Madeleine (AUTHOR), Espada, Mariah (AUTHOR), Law, Tara (AUTHOR), Mansoor, Sanya (AUTHOR), Perrigo, Billy (AUTHOR), Popli, Nik (AUTHOR), Shah, Simmone (AUTHOR), Waxman, Olivia B. (AUTHOR)
Publikováno v:
TIME Magazine. 4/11/2022, Vol. 199 Issue 13/14, p15-15. 3/4p. 1 Color Photograph.
Autor:
Fabio Sippelli, Silvana Briuglia, Chiara Ferraloro, Anna Paola Capra, Emanuele Agolini, Tiziana Abbate, Giorgia Pepe, Tommaso Aversa, Malgorzata Wasniewska, Domenico Corica
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Pseudohypoparathyroidism (PHP) is caused by loss-of-function mutations at the GNAS gene (as in the PHP type 1A; PHP1A), de novo or inherited at heterozygous state, or by epigenetic alterations at the GNAS locus (as in the PHP1B).
Externí odkaz:
https://doaj.org/article/b3347a76c4a2470bb7a3e070a6b215ba