Search research articles
Contact Us
Filters
Showing results (1-10 of 72) with videos related to
Page
of 8
Sort By:
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 mosaicism
Eric Legius, Hilde Brems
The Keio Journal of Medicine
|
December 17, 2013
Legius syndrome, an Update. Molecular pathology of mutations in SPRED1
Hilde Brems, Eric Legius
The Lancet. Oncology
|
May 5, 2009
Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1
Hilde 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 Pathways
Sarah C Borrie, Hilde Brems, Eric Legius, et al.
Pediatric Dermatology
|
November 29, 2023
Capillary malformations in a child caused by a novel HRAS mutation
Dirk 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 tibia
Kjell 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 RASopathy
Sarah C Borrie, Alexa E Horner, Akihiko Yoshimura, et al.
Human Mutation
|
July 4, 2012
Review and update of SPRED1 mutations causing Legius syndrome
Hilde 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 mTOR
Cory M Johannessen, Elizabeth E Reczek, Marianne F James, et al.
Genomics
|
July 6, 2004
Genomic organization and evolution of the NF1 microdeletion region
Thomas De Raedt, Hilde Brems, Catalina Lopez-Correa, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 72) with videos related to
Sort By:
Page
of 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 mosaicism
Eric Legius, Hilde Brems
The Keio Journal of Medicine
|
December 17, 2013
Legius syndrome, an Update. Molecular pathology of mutations in SPRED1
Hilde Brems, Eric Legius
The Lancet. Oncology
|
May 5, 2009
Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1
Hilde 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 Pathways
Sarah C Borrie, Hilde Brems, Eric Legius, et al.
Pediatric Dermatology
|
November 29, 2023
Capillary malformations in a child caused by a novel HRAS mutation
Dirk 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 tibia
Kjell 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 RASopathy
Sarah C Borrie, Alexa E Horner, Akihiko Yoshimura, et al.
Human Mutation
|
July 4, 2012
Review and update of SPRED1 mutations causing Legius syndrome
Hilde 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 mTOR
Cory M Johannessen, Elizabeth E Reczek, Marianne F James, et al.
Genomics
|
July 6, 2004
Genomic organization and evolution of the NF1 microdeletion region
Thomas De Raedt, Hilde Brems, Catalina Lopez-Correa, et al.
Page
of 8