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van den Born

Showing results (571-580 of 717) with videos related to

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Ophthalmology|October 3, 2013
Mutations in the mevalonate kinase (MVK) gene cause nonsyndromic retinitis pigmentosaAnna M Siemiatkowska, L Ingeborgh van den Born, P Martin van Hagen, et al.
Investigative Ophthalmology & Visual Science|April 9, 2010
Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli populationDikla Bandah-Rozenfeld, Karin W Littink, Tamar Ben-Yosef, et al.
International Journal of Epidemiology|April 30, 2026
Acute-phase reactants as predictors of chronic kidney disease incidence in Africans: the population-based prospective RODAM cohort studyMuhulo M Mungamba, Felix P Chilunga, Eva L Van Der Linden, et al.
The Netherlands Journal of Medicine|October 23, 2020
New diagnostic and treatment strategies in renal artery stenosis: a promising pursuit or disappointment foretold?L van de Velde, D Collard, W Spiering, et al.
Investigative Ophthalmology & Visual Science|November 18, 2015
A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis PigmentosaKristof Van Schil, B Jeroen Klevering, Bart P Leroy, et al.
Journal of Hypertension|September 11, 2013
Test characteristics of the aldosterone-to-renin ratio as a screening test for primary aldosteronismPieter M Jansen, Bert-Jan H van den Born, Wijnanda J Frenkel, et al.
Gut Microbes|April 6, 2025
Gut microbiota shift in Ghanaian individuals along the migration axis: the RODAM-Pros cohortBarbara J H Verhaar, Eva L van der Linden, Charles F Hayfron-Benjamin, et al.
Acta Ophthalmologica|November 25, 2025
Vitreoretinal complications and surgical outcomes in patients with X-linked retinoschisisJonathan Hensman, Leo C Hahn, Mary J van Schooneveld, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|November 1, 2016
Blood pressure reduction after gastric bypass surgery is explained by a decrease in cardiac outputPeter M van Brussel, Bas van den Bogaard, Barbara A de Weijer, et al.
American Journal of Human Genetics|August 16, 2006
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosisAnneke I den Hollander, Robert K Koenekoop, Suzanne Yzer, et al.
Pageof 72

Showing results (571-580 of 717) with videos related to

Sort By:
Pageof 72
Ophthalmology|October 3, 2013
Mutations in the mevalonate kinase (MVK) gene cause nonsyndromic retinitis pigmentosaAnna M Siemiatkowska, L Ingeborgh van den Born, P Martin van Hagen, et al.
Investigative Ophthalmology & Visual Science|April 9, 2010
Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli populationDikla Bandah-Rozenfeld, Karin W Littink, Tamar Ben-Yosef, et al.
International Journal of Epidemiology|April 30, 2026
Acute-phase reactants as predictors of chronic kidney disease incidence in Africans: the population-based prospective RODAM cohort studyMuhulo M Mungamba, Felix P Chilunga, Eva L Van Der Linden, et al.
The Netherlands Journal of Medicine|October 23, 2020
New diagnostic and treatment strategies in renal artery stenosis: a promising pursuit or disappointment foretold?L van de Velde, D Collard, W Spiering, et al.
Investigative Ophthalmology & Visual Science|November 18, 2015
A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis PigmentosaKristof Van Schil, B Jeroen Klevering, Bart P Leroy, et al.
Journal of Hypertension|September 11, 2013
Test characteristics of the aldosterone-to-renin ratio as a screening test for primary aldosteronismPieter M Jansen, Bert-Jan H van den Born, Wijnanda J Frenkel, et al.
Gut Microbes|April 6, 2025
Gut microbiota shift in Ghanaian individuals along the migration axis: the RODAM-Pros cohortBarbara J H Verhaar, Eva L van der Linden, Charles F Hayfron-Benjamin, et al.
Acta Ophthalmologica|November 25, 2025
Vitreoretinal complications and surgical outcomes in patients with X-linked retinoschisisJonathan Hensman, Leo C Hahn, Mary J van Schooneveld, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|November 1, 2016
Blood pressure reduction after gastric bypass surgery is explained by a decrease in cardiac outputPeter M van Brussel, Bas van den Bogaard, Barbara A de Weijer, et al.
American Journal of Human Genetics|August 16, 2006
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosisAnneke I den Hollander, Robert K Koenekoop, Suzanne Yzer, et al.
Pageof 72