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Vinciane Dideberg

Showing results (11-20 of 30) with videos related to

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Revue Medicale De Liege|February 13, 2026
[Real-world diagnostic performance of the «Allogenomics» predictive score in a cohort of 185 patients with suspected inherited kidney disease]Cédric Ilbert, Laura Massoz, Bernard Grisart, et al.
Scientific Reports|February 5, 2021
Newborn screening of duchenne muscular dystrophy specifically targeting deletions amenable to exon-skipping therapyPablo Beckers, Jean-Hubert Caberg, Vinciane Dideberg, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|July 18, 2013
Modulating effect of COMT genotype on the brain regions underlying proactive control process during inhibitionMathieu Jaspar, Sarah Genon, Vincenzo Muto, et al.
BMC Medical Genetics|July 14, 2014
Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomaliesAnnette Uwineza, Jean-Hubert Caberg, Janvier Hitayezu, et al.
Journal of Tropical Pediatrics|November 12, 2013
Genetic diagnosis of Duchenne and Becker muscular dystrophy using multiplex ligation-dependent probe amplification in Rwandan patientsAnnette Uwineza, Janvier Hitayezu, Seraphine Murorunkwere, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 11, 2020
Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX DeletionSandrine Petignot, Adrian F Daly, Emilie Castermans, et al.
Pharmacogenetics and Genomics|April 13, 2006
Lymphotoxin alpha gene in Crohn's disease patients: absence of implication in the response to infliximab in a large cohort studyVinciane Dideberg, Edouard Louis, Frédéric Farnir, et al.
Genes|May 4, 2026
The First Case of Kleefstra Syndrome in a Rwandan Patient with Global Developmental DelayNorbert Dukuze, Janvier Hitayezu, Jeanne Primitive Uyisenga, et al.
Pharmacogenetics and Genomics|September 27, 2006
The TNF/ADAM 17 system: implication of an ADAM 17 haplotype in the clinical response to infliximab in Crohn's diseaseVinciane Dideberg, Emilie Théâtre, Frédéric Farnir, et al.
Plos One|August 13, 2013
Altered white matter architecture in BDNF met carriersErik Ziegler, Ariane Foret, Laura Mascetti, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Revue Medicale De Liege|February 13, 2026
[Real-world diagnostic performance of the «Allogenomics» predictive score in a cohort of 185 patients with suspected inherited kidney disease]Cédric Ilbert, Laura Massoz, Bernard Grisart, et al.
Scientific Reports|February 5, 2021
Newborn screening of duchenne muscular dystrophy specifically targeting deletions amenable to exon-skipping therapyPablo Beckers, Jean-Hubert Caberg, Vinciane Dideberg, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|July 18, 2013
Modulating effect of COMT genotype on the brain regions underlying proactive control process during inhibitionMathieu Jaspar, Sarah Genon, Vincenzo Muto, et al.
BMC Medical Genetics|July 14, 2014
Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomaliesAnnette Uwineza, Jean-Hubert Caberg, Janvier Hitayezu, et al.
Journal of Tropical Pediatrics|November 12, 2013
Genetic diagnosis of Duchenne and Becker muscular dystrophy using multiplex ligation-dependent probe amplification in Rwandan patientsAnnette Uwineza, Janvier Hitayezu, Seraphine Murorunkwere, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|June 11, 2020
Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX DeletionSandrine Petignot, Adrian F Daly, Emilie Castermans, et al.
Pharmacogenetics and Genomics|April 13, 2006
Lymphotoxin alpha gene in Crohn's disease patients: absence of implication in the response to infliximab in a large cohort studyVinciane Dideberg, Edouard Louis, Frédéric Farnir, et al.
Genes|May 4, 2026
The First Case of Kleefstra Syndrome in a Rwandan Patient with Global Developmental DelayNorbert Dukuze, Janvier Hitayezu, Jeanne Primitive Uyisenga, et al.
Pharmacogenetics and Genomics|September 27, 2006
The TNF/ADAM 17 system: implication of an ADAM 17 haplotype in the clinical response to infliximab in Crohn's diseaseVinciane Dideberg, Emilie Théâtre, Frédéric Farnir, et al.
Plos One|August 13, 2013
Altered white matter architecture in BDNF met carriersErik Ziegler, Ariane Foret, Laura Mascetti, et al.
Pageof 3