Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Norma Balderrábano-Saucedo"'
Autor:
Arodi Farrera, María Villanueva, Alfredo Vizcaíno, Patricia Medina-Bravo, Norma Balderrábano-Saucedo, Mariana Rives, David Cruz, Elizabeth Hernández-Carbajal, Javier Granados-Riveron, Rocío Sánchez-Urbina
Publikováno v:
Head & Face Medicine, Vol 15, Iss 1, Pp 1-12 (2019)
Abstract Background 22q11.2 deletion syndrome is a medical condition that results from genomic loss at chromosome 22. Affected patients exhibit large variability that ranges from a severe condition to mild symptoms. In addition, the spectrum of clini
Externí odkaz:
https://doaj.org/article/4befd271a73f4c04b2b2a8f0241efdfe
Autor:
Yesica Abril Botello-Flores, Martha Yocupicio-Monroy, Norma Balderrábano-Saucedo, Alejandra Contreras-Ramos
Publikováno v:
Molecular Biology Reports. 49:8953-8973
Heart failure (HF) is a deeply serious clinical problem that remains unsolved. Many reports highlight the cardioprotective properties of mesenchymal stem cells (MSCs), the factors contained in their secretome being particularly important for this fun
Autor:
Yesica Abril Botello-Flores, Martha Yocupicio-Monroy, Norma Balderrábano-Saucedo, Alejandra Contreras-Ramos
Publikováno v:
Molecular Biology Reports. 49:8975-8975
Autor:
Dietmar Schranz, Hakan Akintuerk, Leonard Bailey, Oliver Miera, Friederike Danne, Minoo N. Kavarana, Mac Felmly, Joseph Panzer, Thierry Bove, Daniël De Wolf, Sabine Recla, Iki Adachi, Jeffrery W. Dreyer, Martin A. Chacon, Cansaran Tanidir, Alper Guzeltas, Sertac Haydin, Rene Pretre, Stefano Di Bernado, Marc Gewillig, Bjorn Cools, Brent Gordon, Dexter Cheng, Norma Balderrábano Saucedo, Julio Erdmenger Orellana, Alejandro Bolio Cerdán, Peter Ewert, Gunter Balling, Massimo Padalino, Giovanni Stellin, Biagio Castaldi, Karel Koubský, Roman Gebauer, Jan Janousek, Bohdan Maruszewski, Andrzej Kansy, Michal Kozlowski
Publikováno v:
Circulation. 137:1410-1412
We report the worldwide experience of surgical pulmonary artery banding (PAB) treatment of end-stage left ventricular dilated cardiomyopathy (LV-DCM) with preserved right ventricular function. Pediatric LV-DCM is a leading cause of cardiac death,1,2
Autor:
Dan Hu, Dong Hu, Liwen Liu, Daniel Barr, Yang Liu, Norma Balderrabano-Saucedo, Bo Wang, Feng Zhu, Yumei Xue, Shulin Wu, BaoLiang Song, Heather McManus, Katherine Murphy, Katherine Loes, Arnon Adler, Lorenzo Monserrat, Charles Antzelevitch, Michael H. Gollob, Perry M. Elliott, Hector Barajas-Martinez
Publikováno v:
EBioMedicine, Vol 54, Iss , Pp - (2020)
Background: Although 21 causative mutations have been associated with PRKAG2 syndrome, our understanding of the syndrome remains incomplete. The aim of this project is to further investigate its unique genetic background, clinical manifestations, and
Externí odkaz:
https://doaj.org/article/261fdad085bf4de79b25dd66139363da