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Eric Legius

Showing results (71-80 of 165) with videos related to

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Lancet (London, England)|March 20, 2004
A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4)Carol J Gallione, Gabriela M Repetto, Eric Legius, et al.
The Journal of Biological Chemistry|November 7, 2024
Legius syndrome mutations in the Ras-regulator SPRED1 abolish its membrane localization and potentially cause neurodegenerationYasuko Hirata, Hilde Brems, Seppe Van der Auweraer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 2, 2009
Spred1 is required for synaptic plasticity and hippocampus-dependent learningEllen Denayer, Tariq Ahmed, Hilde Brems, et al.
Human Reproduction (Oxford, England)|February 4, 2017
Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryosEftychia Dimitriadou, Cindy Melotte, Sophie Debrock, et al.
European Journal of Human Genetics : EJHG|April 27, 2021
Identifying challenges in neurofibromatosis: a modified Delphi procedureBritt A E Dhaenens, Rosalie E Ferner, Annette Bakker, et al.
BMC Medical Genetics|September 24, 2009
Pathogenesis of vestibular schwannoma in ring chromosome 22Ellen Denayer, Hilde Brems, Paul de Cock, et al.
Neuroimage. Clinical|June 18, 2014
Characterizing the microstructural basis of "unidentified bright objects" in neurofibromatosis type 1: A combined in vivo multicomponent T2 relaxation and multi-shell diffusion MRI analysisThibo Billiet, Burkhard Mädler, Felice D'Arco, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 16, 2011
Observations on intelligence and behavior in 15 patients with Legius syndromeEllen Denayer, Mie-Jef Descheemaeker, Douglas R Stewart, et al.
Cancers|October 29, 2025
Reply to Taal et al. Comment on "Iasella et al. Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath Tumour. <i>Cancers</i> 2025, <i>17</i>, 1306"Maria Pia Iasella, Dries Ruttens, Daphne Hompes, et al.
Cancers|April 26, 2025
Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath TumourMaria Pia Iasella, Dries Ruttens, Daphne Hompes, et al.
Pageof 17

Showing results (71-80 of 165) with videos related to

Sort By:
Pageof 17
Lancet (London, England)|March 20, 2004
A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4)Carol J Gallione, Gabriela M Repetto, Eric Legius, et al.
The Journal of Biological Chemistry|November 7, 2024
Legius syndrome mutations in the Ras-regulator SPRED1 abolish its membrane localization and potentially cause neurodegenerationYasuko Hirata, Hilde Brems, Seppe Van der Auweraer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 2, 2009
Spred1 is required for synaptic plasticity and hippocampus-dependent learningEllen Denayer, Tariq Ahmed, Hilde Brems, et al.
Human Reproduction (Oxford, England)|February 4, 2017
Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryosEftychia Dimitriadou, Cindy Melotte, Sophie Debrock, et al.
European Journal of Human Genetics : EJHG|April 27, 2021
Identifying challenges in neurofibromatosis: a modified Delphi procedureBritt A E Dhaenens, Rosalie E Ferner, Annette Bakker, et al.
BMC Medical Genetics|September 24, 2009
Pathogenesis of vestibular schwannoma in ring chromosome 22Ellen Denayer, Hilde Brems, Paul de Cock, et al.
Neuroimage. Clinical|June 18, 2014
Characterizing the microstructural basis of "unidentified bright objects" in neurofibromatosis type 1: A combined in vivo multicomponent T2 relaxation and multi-shell diffusion MRI analysisThibo Billiet, Burkhard Mädler, Felice D'Arco, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 16, 2011
Observations on intelligence and behavior in 15 patients with Legius syndromeEllen Denayer, Mie-Jef Descheemaeker, Douglas R Stewart, et al.
Cancers|October 29, 2025
Reply to Taal et al. Comment on "Iasella et al. Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath Tumour. <i>Cancers</i> 2025, <i>17</i>, 1306"Maria Pia Iasella, Dries Ruttens, Daphne Hompes, et al.
Cancers|April 26, 2025
Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath TumourMaria Pia Iasella, Dries Ruttens, Daphne Hompes, et al.
Pageof 17