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Vinciane Dideberg

Showing results (1-10 of 30) with videos related to

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Plos One|May 13, 2024
Association between executive functions and COMT Val108/158Met polymorphism among healthy younger and older adults: A preliminary studyZoltan Apa, Jessica Gilsoul, Vinciane Dideberg, et al.
Kidney International|January 23, 2025
Amelogenesis imperfecta in familial hypomagnesemia with hypercalciuria and nephrocalcinosisInès Vanderheyden, Adeline Jacquinet, Vinciane Dideberg, et al.
Brain and Cognition|February 16, 2015
Modulating effect of COMT Val(158)Met polymorphism on interference resolution during a working memory taskMathieu Jaspar, Vinciane Dideberg, Vincent Bours, et al.
Revue Medicale De Liege|March 12, 2026
[Autosomal dominant polycystic kidney disease]Charlotte Leemans, Laura Massoz, Romain Gillard, et al.
Neurology|July 22, 2020
Reader response: Discrepancy in redetermination of <i>SMN2</i> copy numbers in children with SMATamara Dangouloff, François Boemer, Vinciane Dideberg, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 11, 2014
Influence of COMT Genotype on Antero-posterior Cortical Functional Connectivity Underlying Interference ResolutionMathieu Jaspar, Marine Manard, Vinciane Dideberg, et al.
Revue Medicale De Liege|October 14, 2024
[Neonatal screening for cystic fibrosis in the Liège region : first evaluation after 4 years]Matthieu Thimmesch, François Boemer, Géraldine Luis, et al.
Frontiers in Endocrinology|August 18, 2025
Monogenic etiologies in a cohort of early onset obesity: a real-world experience from BelgiumJulie Harvengt, Muriel Hannon, Leonor Palmeira, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|November 3, 2025
Homozygous Pathogenic MYH3 Variants Associated With Arthrogryposis and Lingual DystoniaCharlotte Mouraux, Claire Fouquet, Keith Durkin, et al.
Neuromuscular Disorders : NMD|April 30, 2019
Newborn screening for SMA in Southern BelgiumFrançois Boemer, Jean-Hubert Caberg, Vinciane Dideberg, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Plos One|May 13, 2024
Association between executive functions and COMT Val108/158Met polymorphism among healthy younger and older adults: A preliminary studyZoltan Apa, Jessica Gilsoul, Vinciane Dideberg, et al.
Kidney International|January 23, 2025
Amelogenesis imperfecta in familial hypomagnesemia with hypercalciuria and nephrocalcinosisInès Vanderheyden, Adeline Jacquinet, Vinciane Dideberg, et al.
Brain and Cognition|February 16, 2015
Modulating effect of COMT Val(158)Met polymorphism on interference resolution during a working memory taskMathieu Jaspar, Vinciane Dideberg, Vincent Bours, et al.
Revue Medicale De Liege|March 12, 2026
[Autosomal dominant polycystic kidney disease]Charlotte Leemans, Laura Massoz, Romain Gillard, et al.
Neurology|July 22, 2020
Reader response: Discrepancy in redetermination of <i>SMN2</i> copy numbers in children with SMATamara Dangouloff, François Boemer, Vinciane Dideberg, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 11, 2014
Influence of COMT Genotype on Antero-posterior Cortical Functional Connectivity Underlying Interference ResolutionMathieu Jaspar, Marine Manard, Vinciane Dideberg, et al.
Revue Medicale De Liege|October 14, 2024
[Neonatal screening for cystic fibrosis in the Liège region : first evaluation after 4 years]Matthieu Thimmesch, François Boemer, Géraldine Luis, et al.
Frontiers in Endocrinology|August 18, 2025
Monogenic etiologies in a cohort of early onset obesity: a real-world experience from BelgiumJulie Harvengt, Muriel Hannon, Leonor Palmeira, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|November 3, 2025
Homozygous Pathogenic MYH3 Variants Associated With Arthrogryposis and Lingual DystoniaCharlotte Mouraux, Claire Fouquet, Keith Durkin, et al.
Neuromuscular Disorders : NMD|April 30, 2019
Newborn screening for SMA in Southern BelgiumFrançois Boemer, Jean-Hubert Caberg, Vinciane Dideberg, et al.
Pageof 3