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The World Allergy Organization Journal|August 7, 2019
YRNAs overexpression and potential implications in allergyMaría Isidoro-García, Asunción García-Sánchez, Catalina Sanz, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 26, 2024
PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patientsJesús Martín-Valbuena, Nerea Gestoso-Uzal, María Justel-Rodríguez, et al.
The Journal of Allergy and Clinical Immunology. in Practice|November 15, 2017
Cluster Analysis Identifies 3 Phenotypes within Allergic AsthmaMaría Paz Sendín-Hernández, Carmelo Ávila-Zarza, Catalina Sanz, et al.
Frontiers in Psychiatry|March 14, 2022
Case Report: Pharmacogenetics Applied to Precision Psychiatry Could Explain the Outcome of a Patient With a New <i>CYP2D6</i> GenotypeElena Marcos-Vadillo, Lorena Carrascal-Laso, Ignacio Ramos-Gallego, et al.
Journal of Clinical Medicine|July 27, 2024
Clinical and Genetic Characterization of a Cohort of Small-for-Gestational-Age Patients: Cost-Effectiveness of Whole-Exome Sequencing and Effectiveness of Treatment with GHRamón Arroyo-Ruiz, Cristina Urbano-Ruiz, María Belén García-Berrocal, et al.
Journal of Personalized Medicine|December 23, 2020
Application of a Pharmacogenetics-Based Precision Medicine Model (5SPM) to Psychotic Patients That Presented Poor Response to Neuroleptic TherapyLorena Carrascal-Laso, Manuel Ángel Franco-Martín, María Belén García-Berrocal, et al.
International Journal of Molecular Sciences|November 9, 2024
A Comparison of Molecular Techniques for Improving the Methodology in the Laboratory of PharmacogeneticsMaría Celsa Peña-Martín, Elena Marcos-Vadillo, Belén García-Berrocal, et al.
Pharmacogenomics and Personalized Medicine|August 25, 2021
Economic Impact of the Application of a Precision Medicine Model (5SPM) on Psychotic PatientsLorena Carrascal-Laso, Manuel Ángel Franco-Martín, Elena Marcos-Vadillo, et al.
Pharmaceutics|January 21, 2022
Ten Years of Experience Support Pharmacogenetic Testing to Guide Individualized Drug TherapyMaría Celsa Peña-Martín, Belén García-Berrocal, Almudena Sánchez-Martín, et al.
Revista Espanola De Cardiologia (English Ed.)|October 3, 2020
A rare HCN4 variant with combined sinus bradycardia, left atrial dilatation, and hypertrabeculation/left ventricular noncompaction phenotypeMarta Alonso-Fernández-Gatta, María Gallego-Delgado, Ricardo Caballero, et al.
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