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Forensic Science International. Genetics
|
August 8, 2018
Molecular autopsy in a cohort of infants died suddenly at rest
Oscar Campuzano, Pilar Beltramo, Anna Fernandez, et al.
Journal of Clinical Medicine
|
August 12, 2022
Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review
Antonio Oliva, Simone Grassi, Vilma Pinchi, et al.
Familial Cancer
|
March 13, 2016
Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer
Aryana S Jacobs, Marc D Schwartz, Heiddis Valdimarsdottir, et al.
JAMA Network Open
|
September 15, 2022
Recanalization Treatments for Pediatric Acute Ischemic Stroke in France
Manoëlle Kossorotoff, Basile Kerleroux, Grégoire Boulouis, et al.
Frontiers in Genetics
|
June 4, 2019
Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies
Oscar Campuzano, Anna Fernandez-Falgueras, Georgia Sarquella-Brugada, et al.
International Archives of Occupational and Environmental Health
|
January 27, 2026
Systematic review update of organisational-level mental health promotion interventions: evidence from healthcare, construction, and telework-based mobile work settings
Eleftherios Giovanis, Oznur Ozdamar, Birgit Aust, et al.
Human Genetics
|
September 21, 2021
Clinical impact of rare variants associated with inherited channelopathies: a 5-year update
Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, et al.
International Journal of Legal Medicine
|
January 24, 2023
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort
Estefanía Martinez-Barrios, Georgia Sarquella-Brugada, Alexandra Perez-Serra, et al.
Forensic Science International. Genetics
|
April 6, 2020
Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
Jesus Mates, Irene Mademont-Soler, Anna Fernandez-Falgueras, et al.
The Lancet. Neurology
|
February 20, 2018
The effect of LRRK2 mutations on the cholinergic system in manifest and premanifest stages of Parkinson's disease: a cross-sectional PET study
Shu-Ying Liu, Daryl J Wile, Jessie Fanglu Fu, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 85) with videos related to
Sort By:
Page
of 9
Forensic Science International. Genetics
|
August 8, 2018
Molecular autopsy in a cohort of infants died suddenly at rest
Oscar Campuzano, Pilar Beltramo, Anna Fernandez, et al.
Journal of Clinical Medicine
|
August 12, 2022
Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review
Antonio Oliva, Simone Grassi, Vilma Pinchi, et al.
Familial Cancer
|
March 13, 2016
Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer
Aryana S Jacobs, Marc D Schwartz, Heiddis Valdimarsdottir, et al.
JAMA Network Open
|
September 15, 2022
Recanalization Treatments for Pediatric Acute Ischemic Stroke in France
Manoëlle Kossorotoff, Basile Kerleroux, Grégoire Boulouis, et al.
Frontiers in Genetics
|
June 4, 2019
Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies
Oscar Campuzano, Anna Fernandez-Falgueras, Georgia Sarquella-Brugada, et al.
International Archives of Occupational and Environmental Health
|
January 27, 2026
Systematic review update of organisational-level mental health promotion interventions: evidence from healthcare, construction, and telework-based mobile work settings
Eleftherios Giovanis, Oznur Ozdamar, Birgit Aust, et al.
Human Genetics
|
September 21, 2021
Clinical impact of rare variants associated with inherited channelopathies: a 5-year update
Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, et al.
International Journal of Legal Medicine
|
January 24, 2023
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort
Estefanía Martinez-Barrios, Georgia Sarquella-Brugada, Alexandra Perez-Serra, et al.
Forensic Science International. Genetics
|
April 6, 2020
Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
Jesus Mates, Irene Mademont-Soler, Anna Fernandez-Falgueras, et al.
The Lancet. Neurology
|
February 20, 2018
The effect of LRRK2 mutations on the cholinergic system in manifest and premanifest stages of Parkinson's disease: a cross-sectional PET study
Shu-Ying Liu, Daryl J Wile, Jessie Fanglu Fu, et al.
Page
of 9