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Showing results (261-270 of 265) with videos related to

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Gastroenterology|January 29, 2013
Risk of cancer in cases of suspected lynch syndrome without germline mutationMaría Rodríguez-Soler, Lucía Pérez-Carbonell, Carla Guarinos, et al.
Journal of Investigational Allergology & Clinical Immunology|May 3, 2022
Exacerbations Among Patients With Asthma Are Largely Dependent on the Presence of MultimorbidityJ Domínguez-Ortega, J A Luna-Porta, J M Olaguibel, et al.
The Lancet. Digital Health|May 27, 2026
Artificial intelligence analysis of temporalis muscle thickness for monitoring sarcopenia and clinical outcomes in individuals with paediatric brain tumours: a retrospective cohort studyAnna Zapaishchykova, John Zielke, Divyanshu Tak, et al.
Database : the Journal of Biological Databases and Curation|July 5, 2024
SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish populationJosé M Moreno-Cabrera, Lidia Feliubadaló, Marta Pineda, et al.
The Lancet. Oncology|November 27, 2022
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk SyndromesJosé Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, et al.
Pageof 27

Showing results (261-270 of 265) with videos related to

Sort By:
Pageof 27
You have reached the last page of results.This site can display upto 265 results.
Gastroenterology|January 29, 2013
Risk of cancer in cases of suspected lynch syndrome without germline mutationMaría Rodríguez-Soler, Lucía Pérez-Carbonell, Carla Guarinos, et al.
Journal of Investigational Allergology & Clinical Immunology|May 3, 2022
Exacerbations Among Patients With Asthma Are Largely Dependent on the Presence of MultimorbidityJ Domínguez-Ortega, J A Luna-Porta, J M Olaguibel, et al.
The Lancet. Digital Health|May 27, 2026
Artificial intelligence analysis of temporalis muscle thickness for monitoring sarcopenia and clinical outcomes in individuals with paediatric brain tumours: a retrospective cohort studyAnna Zapaishchykova, John Zielke, Divyanshu Tak, et al.
Database : the Journal of Biological Databases and Curation|July 5, 2024
SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish populationJosé M Moreno-Cabrera, Lidia Feliubadaló, Marta Pineda, et al.
The Lancet. Oncology|November 27, 2022
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk SyndromesJosé Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, et al.
Pageof 27