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Showing results (511-520 of 566) with videos related to

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International Journal of Cardiology|March 11, 2025
Beyond the gut: Systemic levels of short-chain fatty acids are altered in patients with heart failureC L Palm, S de Wit, T M Gorter, et al.
European Journal of Human Genetics : EJHG|March 12, 2020
De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disabilityIris G M Wijnen, Hermine E Veenstra-Knol, Fleur Vansenne, et al.
International Journal of Cardiology|March 4, 2021
Diagnostic yield of targeted next generation sequencing in 2002 Dutch cardiomyopathy patientsMohamed Z Alimohamed, Lennart F Johansson, Anna Posafalvi, et al.
Familial Cancer|September 26, 2012
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature reviewA P Knopperts, M Nielsen, R C Niessen, et al.
Neuro-Oncology Practice|October 13, 2025
Bevacizumab for symptomatic cerebral radiation necrosis after radiation of high-grade glioma or brain metastases - when and for whom?Lente L Kroon, Edith M T Dieleman, Vera C Keil, et al.
European Journal of Cancer (Oxford, England : 1990)|March 8, 2011
Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelinesJohanna C Herkert, Renée C Niessen, Maria J W Olderode-Berends, et al.
Journal of the American Chemical Society|November 22, 2007
Stepwise noncovalent synthesis leading to dendrimer-based assemblies in waterThomas M Hermans, Maarten A C Broeren, Nikos Gomopoulos, et al.
Nature Medicine|July 2, 2024
Effects of intermittent senolytic therapy on bone metabolism in postmenopausal women: a phase 2 randomized controlled trialJoshua N Farr, Elizabeth J Atkinson, Sara J Achenbach, et al.
European Journal of Human Genetics : EJHG|August 30, 2021
TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobilityAafke Engwerda, Erika K S M Leenders, Barbara Frentz, et al.
Journal of Alzheimer'S Disease : JAD|September 24, 2016
White Matter Hyperintensities Potentiate Hippocampal Volume Reduction in Non-Demented Older Individuals with Abnormal Amyloid-βWhitney M Freeze, Heidi I L Jacobs, Ed H Gronenschild, et al.
Pageof 57

Showing results (511-520 of 566) with videos related to

Sort By:
Pageof 57
International Journal of Cardiology|March 11, 2025
Beyond the gut: Systemic levels of short-chain fatty acids are altered in patients with heart failureC L Palm, S de Wit, T M Gorter, et al.
European Journal of Human Genetics : EJHG|March 12, 2020
De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disabilityIris G M Wijnen, Hermine E Veenstra-Knol, Fleur Vansenne, et al.
International Journal of Cardiology|March 4, 2021
Diagnostic yield of targeted next generation sequencing in 2002 Dutch cardiomyopathy patientsMohamed Z Alimohamed, Lennart F Johansson, Anna Posafalvi, et al.
Familial Cancer|September 26, 2012
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature reviewA P Knopperts, M Nielsen, R C Niessen, et al.
Neuro-Oncology Practice|October 13, 2025
Bevacizumab for symptomatic cerebral radiation necrosis after radiation of high-grade glioma or brain metastases - when and for whom?Lente L Kroon, Edith M T Dieleman, Vera C Keil, et al.
European Journal of Cancer (Oxford, England : 1990)|March 8, 2011
Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelinesJohanna C Herkert, Renée C Niessen, Maria J W Olderode-Berends, et al.
Journal of the American Chemical Society|November 22, 2007
Stepwise noncovalent synthesis leading to dendrimer-based assemblies in waterThomas M Hermans, Maarten A C Broeren, Nikos Gomopoulos, et al.
Nature Medicine|July 2, 2024
Effects of intermittent senolytic therapy on bone metabolism in postmenopausal women: a phase 2 randomized controlled trialJoshua N Farr, Elizabeth J Atkinson, Sara J Achenbach, et al.
European Journal of Human Genetics : EJHG|August 30, 2021
TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobilityAafke Engwerda, Erika K S M Leenders, Barbara Frentz, et al.
Journal of Alzheimer'S Disease : JAD|September 24, 2016
White Matter Hyperintensities Potentiate Hippocampal Volume Reduction in Non-Demented Older Individuals with Abnormal Amyloid-βWhitney M Freeze, Heidi I L Jacobs, Ed H Gronenschild, et al.
Pageof 57