Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Stanescu

Showing results (661-670 of 940) with videos related to

Pageof 94
Sort By:
The New England Journal of Medicine|February 4, 2011
NT5E mutations and arterial calcificationsCynthia St Hilaire, Shira G Ziegler, Thomas C Markello, et al.
Vaccines|January 27, 2021
A Rapid Systematic Review of Public Responses to Health Messages Encouraging Vaccination against Infectious Diseases in a Pandemic or EpidemicSadie Lawes-Wickwar, Daniela Ghio, Mei Yee Tang, et al.
Elife|September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valvesMelanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
Magnetic Resonance in Medicine|September 21, 2022
The future of MRI in radiation therapy: Challenges and opportunities for the MR communityRosie J Goodburn, Marielle E P Philippens, Thierry L Lefebvre, et al.
JIMD Reports|March 14, 2022
Diagnosis of inborn errors of metabolism within the expanded newborn screening in the Madrid regionÁlvaro Martín-Rivada, Laura Palomino Pérez, Pedro Ruiz-Sala, et al.
The Lancet. Oncology|July 19, 2024
Celiac plexus radiosurgery for pain management in advanced cancer: a multicentre, single-arm, phase 2 trialYaacov R Lawrence, Marcin Miszczyk, Laura A Dawson, et al.
Journal of Clinical Medicine|November 6, 2019
Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized TreatmentIrene Bravo-Alonso, Rosa Navarrete, Ana Isabel Vega, et al.
Journal of the American Society of Nephrology : JASN|April 25, 2009
HNF1B mutations associate with hypomagnesemia and renal magnesium wastingShazia Adalat, Adrian S Woolf, Karen A Johnstone, et al.
PLOS Digital Health|March 28, 2023
Developing better digital health measures of Parkinson's disease using free living data and a crowdsourced data analysis challengeSolveig K Sieberts, Henryk Borzymowski, Yuanfang Guan, et al.
Revista Espanola De Salud Publica|December 29, 2020
[Newborn Screening Program in the Community of Madrid: evaluation of positive cases.]Ana Cambra Conejero, Laura Martínez Figueras, Alicia Ortiz Temprado, et al.
Pageof 94

Showing results (661-670 of 940) with videos related to

Sort By:
Pageof 94
The New England Journal of Medicine|February 4, 2011
NT5E mutations and arterial calcificationsCynthia St Hilaire, Shira G Ziegler, Thomas C Markello, et al.
Vaccines|January 27, 2021
A Rapid Systematic Review of Public Responses to Health Messages Encouraging Vaccination against Infectious Diseases in a Pandemic or EpidemicSadie Lawes-Wickwar, Daniela Ghio, Mei Yee Tang, et al.
Elife|September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valvesMelanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
Magnetic Resonance in Medicine|September 21, 2022
The future of MRI in radiation therapy: Challenges and opportunities for the MR communityRosie J Goodburn, Marielle E P Philippens, Thierry L Lefebvre, et al.
JIMD Reports|March 14, 2022
Diagnosis of inborn errors of metabolism within the expanded newborn screening in the Madrid regionÁlvaro Martín-Rivada, Laura Palomino Pérez, Pedro Ruiz-Sala, et al.
The Lancet. Oncology|July 19, 2024
Celiac plexus radiosurgery for pain management in advanced cancer: a multicentre, single-arm, phase 2 trialYaacov R Lawrence, Marcin Miszczyk, Laura A Dawson, et al.
Journal of Clinical Medicine|November 6, 2019
Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized TreatmentIrene Bravo-Alonso, Rosa Navarrete, Ana Isabel Vega, et al.
Journal of the American Society of Nephrology : JASN|April 25, 2009
HNF1B mutations associate with hypomagnesemia and renal magnesium wastingShazia Adalat, Adrian S Woolf, Karen A Johnstone, et al.
PLOS Digital Health|March 28, 2023
Developing better digital health measures of Parkinson's disease using free living data and a crowdsourced data analysis challengeSolveig K Sieberts, Henryk Borzymowski, Yuanfang Guan, et al.
Revista Espanola De Salud Publica|December 29, 2020
[Newborn Screening Program in the Community of Madrid: evaluation of positive cases.]Ana Cambra Conejero, Laura Martínez Figueras, Alicia Ortiz Temprado, et al.
Pageof 94