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van der Linde

Showing results (651-660 of 692) with videos related to

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Human Molecular Genetics|October 24, 2013
Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation-differentiation balance early in life and optic nerve degeneration at old ageAdriana I Iglesias, Henriët Springelkamp, Herma van der Linde, et al.
Gastric Cancer : Official Journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association|January 13, 2026
Hospital variation in surgical outcomes for gastric cancer: the impact of case-mix and treatment across a global cohortSander J M van Hootegem, Margrietha van der Linde, Marcel A Schneider, et al.
American Journal of Human Genetics|April 16, 2019
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of MicrogliaNynke Oosterhof, Irene J Chang, Ehsan Ghayoor Karimiani, et al.
Human Molecular Genetics|April 25, 2002
Mutations in TITF-1 are associated with benign hereditary choreaGuido J Breedveld, Jeroen W F van Dongen, Cesare Danesino, et al.
Epidemiology and Infection|May 12, 2009
Norovirus outbreaks in nursing homes: the evaluation of infection control measuresI H M Friesema, H Vennema, J C M Heijne, et al.
Acta Neuropathologica|June 17, 2022
Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophyWoutje M Berdowski, Herma C van der Linde, Marjolein Breur, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|June 5, 2020
Cardiac telerehabilitation as an alternative to centre-based cardiac rehabilitationR W M Brouwers, H J van Exel, J M C van Hal, et al.
Canadian Journal of Kidney Health and Disease|July 16, 2026
Defining a High-Quality Living Kidney Donor Evaluation: A Delphi Survey and Consensus Conference Summary ReportSeychelle Yohanna, Kyla L Naylor, Linnea Holtby, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2002
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactylyLaura A Lettice, Taizo Horikoshi, Simon J H Heaney, et al.
Archives of Disease in Childhood|February 4, 2019
Evaluation of the Dutch neonatal screening for congenital adrenal hyperplasiaAnnelieke A A van der Linde, Yvonne Schönbeck, Hetty J van der Kamp, et al.
Pageof 70

Showing results (651-660 of 692) with videos related to

Sort By:
Pageof 70
Human Molecular Genetics|October 24, 2013
Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation-differentiation balance early in life and optic nerve degeneration at old ageAdriana I Iglesias, Henriët Springelkamp, Herma van der Linde, et al.
Gastric Cancer : Official Journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association|January 13, 2026
Hospital variation in surgical outcomes for gastric cancer: the impact of case-mix and treatment across a global cohortSander J M van Hootegem, Margrietha van der Linde, Marcel A Schneider, et al.
American Journal of Human Genetics|April 16, 2019
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of MicrogliaNynke Oosterhof, Irene J Chang, Ehsan Ghayoor Karimiani, et al.
Human Molecular Genetics|April 25, 2002
Mutations in TITF-1 are associated with benign hereditary choreaGuido J Breedveld, Jeroen W F van Dongen, Cesare Danesino, et al.
Epidemiology and Infection|May 12, 2009
Norovirus outbreaks in nursing homes: the evaluation of infection control measuresI H M Friesema, H Vennema, J C M Heijne, et al.
Acta Neuropathologica|June 17, 2022
Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophyWoutje M Berdowski, Herma C van der Linde, Marjolein Breur, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|June 5, 2020
Cardiac telerehabilitation as an alternative to centre-based cardiac rehabilitationR W M Brouwers, H J van Exel, J M C van Hal, et al.
Canadian Journal of Kidney Health and Disease|July 16, 2026
Defining a High-Quality Living Kidney Donor Evaluation: A Delphi Survey and Consensus Conference Summary ReportSeychelle Yohanna, Kyla L Naylor, Linnea Holtby, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2002
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactylyLaura A Lettice, Taizo Horikoshi, Simon J H Heaney, et al.
Archives of Disease in Childhood|February 4, 2019
Evaluation of the Dutch neonatal screening for congenital adrenal hyperplasiaAnnelieke A A van der Linde, Yvonne Schönbeck, Hetty J van der Kamp, et al.
Pageof 70