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Showing results (711-720 of 734) with videos related to

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World Journal for Pediatric & Congenital Heart Surgery|January 7, 2021
Heart Transplantation for Pediatric and Congenital Cardiac Disease: A Comparison of Two Eras over 23 Years and 188 Transplants at a Single InstitutionGenevieve C Tuite, James A Quintessenza, Alfred Asante-Korang, et al.
Multiple Sclerosis and Related Disorders|June 4, 2018
Validating the portal population of the United Kingdom Multiple Sclerosis RegisterR M Middleton, W J Rodgers, J Chataway, et al.
Canada Communicable Disease Report = Releve Des Maladies Transmissibles Au Canada|October 9, 2024
Mathematical modelling for pandemic preparedness in Canada: Learning from COVID-19Nicholas H Ogden, Emily S Acheson, Kevin Brown, et al.
American Journal of Human Genetics|March 16, 2007
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsStacey Melquist, David W Craig, Matthew J Huentelman, et al.
The Lancet. Infectious Diseases|February 4, 2018
Molecular surveillance of norovirus, 2005-16: an epidemiological analysis of data collected from the NoroNet networkJanko van Beek, Miranda de Graaf, Haider Al-Hello, et al.
Frontiers in Neurology|July 19, 2021
Best Practices in the Clinical Management of Progressive Supranuclear Palsy and Corticobasal Syndrome: A Consensus Statement of the CurePSP Centers of CareBrent Bluett, Alexander Y Pantelyat, Irene Litvan, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
BMJ Open|May 17, 2023
ADAMS project: a genetic Association study in individuals from Diverse Ancestral backgrounds with Multiple Sclerosis based in the UKBenjamin M Jacobs, Luisa Schalk, Angie Dunne, et al.
Nature|July 12, 2023
Diverse organic-mineral associations in Jezero crater, MarsSunanda Sharma, Ryan D Roppel, Ashley E Murphy, et al.
Journal of Inherited Metabolic Disease|July 19, 2020
Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestionsBobby G Ng, Erik A Eklund, Sergey A Shiryaev, et al.
Pageof 74

Showing results (711-720 of 734) with videos related to

Sort By:
Pageof 74
World Journal for Pediatric & Congenital Heart Surgery|January 7, 2021
Heart Transplantation for Pediatric and Congenital Cardiac Disease: A Comparison of Two Eras over 23 Years and 188 Transplants at a Single InstitutionGenevieve C Tuite, James A Quintessenza, Alfred Asante-Korang, et al.
Multiple Sclerosis and Related Disorders|June 4, 2018
Validating the portal population of the United Kingdom Multiple Sclerosis RegisterR M Middleton, W J Rodgers, J Chataway, et al.
Canada Communicable Disease Report = Releve Des Maladies Transmissibles Au Canada|October 9, 2024
Mathematical modelling for pandemic preparedness in Canada: Learning from COVID-19Nicholas H Ogden, Emily S Acheson, Kevin Brown, et al.
American Journal of Human Genetics|March 16, 2007
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsStacey Melquist, David W Craig, Matthew J Huentelman, et al.
The Lancet. Infectious Diseases|February 4, 2018
Molecular surveillance of norovirus, 2005-16: an epidemiological analysis of data collected from the NoroNet networkJanko van Beek, Miranda de Graaf, Haider Al-Hello, et al.
Frontiers in Neurology|July 19, 2021
Best Practices in the Clinical Management of Progressive Supranuclear Palsy and Corticobasal Syndrome: A Consensus Statement of the CurePSP Centers of CareBrent Bluett, Alexander Y Pantelyat, Irene Litvan, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
BMJ Open|May 17, 2023
ADAMS project: a genetic Association study in individuals from Diverse Ancestral backgrounds with Multiple Sclerosis based in the UKBenjamin M Jacobs, Luisa Schalk, Angie Dunne, et al.
Nature|July 12, 2023
Diverse organic-mineral associations in Jezero crater, MarsSunanda Sharma, Ryan D Roppel, Ashley E Murphy, et al.
Journal of Inherited Metabolic Disease|July 19, 2020
Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestionsBobby G Ng, Erik A Eklund, Sergey A Shiryaev, et al.
Pageof 74