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Hilde Brems

Showing results (1-10 of 72) with videos related to

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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 1, 2020
Genetic basis of neurofibromatosis type 1 and related conditions, including mosaicismEric Legius, Hilde Brems
The Keio Journal of Medicine|December 17, 2013
Legius syndrome, an Update. Molecular pathology of mutations in SPRED1Hilde Brems, Eric Legius
The Lancet. Oncology|May 5, 2009
Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1Hilde Brems, Eline Beert, Thomy de Ravel, et al.
Annual Review of Genomics and Human Genetics|September 2, 2017
Cognitive Dysfunctions in Intellectual Disabilities: The Contributions of the Ras-MAPK and PI3K-AKT-mTOR PathwaysSarah C Borrie, Hilde Brems, Eric Legius, et al.
Pediatric Dermatology|November 29, 2023
Capillary malformations in a child caused by a novel HRAS mutationDirk van Gysel, Hannelore de Maeseneer, Eric Legius, et al.
European Journal of Pediatrics|August 14, 2016
Prevalence of neurofibromatosis type 1 in congenital pseudarthrosis of the tibiaKjell Van Royen, Hilde Brems, Eric Legius, et al.
Genes, Brain, and Behavior|February 24, 2021
Impaired instrumental learning in Spred1<sup>-/-</sup> mice, a model for a rare RASopathySarah C Borrie, Alexa E Horner, Akihiko Yoshimura, et al.
Human Mutation|July 4, 2012
Review and update of SPRED1 mutations causing Legius syndromeHilde Brems, Eric Pasmant, Rick Van Minkelen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 7, 2005
The NF1 tumor suppressor critically regulates TSC2 and mTORCory M Johannessen, Elizabeth E Reczek, Marianne F James, et al.
Genomics|July 6, 2004
Genomic organization and evolution of the NF1 microdeletion regionThomas De Raedt, Hilde Brems, Catalina Lopez-Correa, et al.
Pageof 8

Showing results (1-10 of 72) with videos related to

Sort By:
Pageof 8
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 1, 2020
Genetic basis of neurofibromatosis type 1 and related conditions, including mosaicismEric Legius, Hilde Brems
The Keio Journal of Medicine|December 17, 2013
Legius syndrome, an Update. Molecular pathology of mutations in SPRED1Hilde Brems, Eric Legius
The Lancet. Oncology|May 5, 2009
Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1Hilde Brems, Eline Beert, Thomy de Ravel, et al.
Annual Review of Genomics and Human Genetics|September 2, 2017
Cognitive Dysfunctions in Intellectual Disabilities: The Contributions of the Ras-MAPK and PI3K-AKT-mTOR PathwaysSarah C Borrie, Hilde Brems, Eric Legius, et al.
Pediatric Dermatology|November 29, 2023
Capillary malformations in a child caused by a novel HRAS mutationDirk van Gysel, Hannelore de Maeseneer, Eric Legius, et al.
European Journal of Pediatrics|August 14, 2016
Prevalence of neurofibromatosis type 1 in congenital pseudarthrosis of the tibiaKjell Van Royen, Hilde Brems, Eric Legius, et al.
Genes, Brain, and Behavior|February 24, 2021
Impaired instrumental learning in Spred1<sup>-/-</sup> mice, a model for a rare RASopathySarah C Borrie, Alexa E Horner, Akihiko Yoshimura, et al.
Human Mutation|July 4, 2012
Review and update of SPRED1 mutations causing Legius syndromeHilde Brems, Eric Pasmant, Rick Van Minkelen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 7, 2005
The NF1 tumor suppressor critically regulates TSC2 and mTORCory M Johannessen, Elizabeth E Reczek, Marianne F James, et al.
Genomics|July 6, 2004
Genomic organization and evolution of the NF1 microdeletion regionThomas De Raedt, Hilde Brems, Catalina Lopez-Correa, et al.
Pageof 8