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Raquel Flores

Showing results (31-40 of 51) with videos related to

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Journal of Medical Genetics|February 10, 2015
Metabolic abnormalities in Williams-Beuren syndromeMaría Gabriela Palacios-Verdú, Maria Segura-Puimedon, Cristina Borralleras, et al.
Journal of Medical Genetics|August 16, 2019
Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndromeMarta Codina-Sola, Mar Costa-Roger, Debora Pérez-García, et al.
Journal of the American College of Surgeons|March 25, 2016
C-Reactive Protein and Procalcitonin as Early Markers of Septic Complications after Laparoscopic Sleeve Gastrectomy in Morbidly Obese Patients Within an Enhanced Recovery After Surgery ProgramJosé Luis Muñoz, Jaime Ruiz-Tovar, Elena Miranda, et al.
International Journal of Obesity (2005)|March 31, 2019
Heterozygous rare genetic variants in non-syndromic early-onset obesityClara Serra-Juhé, Gabriel Á Martos-Moreno, Francesc Bou de Pieri, et al.
Surgical Endoscopy|March 10, 2018
Procalcitonin and C-reactive protein as early markers of anastomotic leak after laparoscopic colorectal surgery within an enhanced recovery after surgery (ERAS) programJosé Luis Muñoz, María Oliva Alvarez, Vicent Cuquerella, et al.
The Journal of Clinical Investigation|November 27, 2007
Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disordersMiguel Castelo-Branco, Mafalda Mendes, Ana Raquel Sebastião, et al.
JACC. Case Reports|August 22, 2025
Transcatheter Edge-to-Edge Repair for Mitral Regurgitation in Complex Post-Surgical AnatomyMaría Salgado Barquinero, Marcel Almendárez Lacayo, Raquel Flores Belinchón, et al.
Plos Genetics|May 11, 2017
Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variantsClara Serra-Juhé, Gabriel Á Martos-Moreno, Francesc Bou de Pieri, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|June 14, 2024
A proteomic approach supports the clinical relevance of TAT-Cx43<sub>266-283</sub> in glioblastomaSara G Pelaz, Raquel Flores-Hernández, Tatjana Vujic, et al.
EMBO Molecular Medicine|February 1, 2014
Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiencyJesús Argente, Raquel Flores, Armand Gutiérrez-Arumí, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|February 10, 2015
Metabolic abnormalities in Williams-Beuren syndromeMaría Gabriela Palacios-Verdú, Maria Segura-Puimedon, Cristina Borralleras, et al.
Journal of Medical Genetics|August 16, 2019
Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndromeMarta Codina-Sola, Mar Costa-Roger, Debora Pérez-García, et al.
Journal of the American College of Surgeons|March 25, 2016
C-Reactive Protein and Procalcitonin as Early Markers of Septic Complications after Laparoscopic Sleeve Gastrectomy in Morbidly Obese Patients Within an Enhanced Recovery After Surgery ProgramJosé Luis Muñoz, Jaime Ruiz-Tovar, Elena Miranda, et al.
International Journal of Obesity (2005)|March 31, 2019
Heterozygous rare genetic variants in non-syndromic early-onset obesityClara Serra-Juhé, Gabriel Á Martos-Moreno, Francesc Bou de Pieri, et al.
Surgical Endoscopy|March 10, 2018
Procalcitonin and C-reactive protein as early markers of anastomotic leak after laparoscopic colorectal surgery within an enhanced recovery after surgery (ERAS) programJosé Luis Muñoz, María Oliva Alvarez, Vicent Cuquerella, et al.
The Journal of Clinical Investigation|November 27, 2007
Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disordersMiguel Castelo-Branco, Mafalda Mendes, Ana Raquel Sebastião, et al.
JACC. Case Reports|August 22, 2025
Transcatheter Edge-to-Edge Repair for Mitral Regurgitation in Complex Post-Surgical AnatomyMaría Salgado Barquinero, Marcel Almendárez Lacayo, Raquel Flores Belinchón, et al.
Plos Genetics|May 11, 2017
Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variantsClara Serra-Juhé, Gabriel Á Martos-Moreno, Francesc Bou de Pieri, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|June 14, 2024
A proteomic approach supports the clinical relevance of TAT-Cx43<sub>266-283</sub> in glioblastomaSara G Pelaz, Raquel Flores-Hernández, Tatjana Vujic, et al.
EMBO Molecular Medicine|February 1, 2014
Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiencyJesús Argente, Raquel Flores, Armand Gutiérrez-Arumí, et al.
Pageof 6