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Ellen Denayer

Showing results (1-10 of 26) with videos related to

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European Journal of Pediatrics|July 6, 2007
What's new in the neuro-cardio-facial-cutaneous syndromes?Ellen Denayer, Eric Legius
Acta Dermato-Venereologica|March 10, 2020
Legius Syndrome and its Relationship with Neurofibromatosis Type 1Ellen Denayer, Eric Legius
Ophthalmic Genetics|May 6, 2021
Two siblings with Heimler syndrome caused by PEX1 variants: follow-up of ophthalmologic findingsDorien Herijgers, Ellen Denayer, Irina Balikova, et al.
Journal of Medical Genetics|November 23, 2025
ACTH-secreting atypical carcinoid lung tumour expanding the Lynch syndrome spectrumKevin Van Compernolle, Jacques Van Huysse, Kathleen B M Claes, et al.
European Journal of Medical Genetics|March 23, 2010
Investigation of gene dosage imbalances in patients with Noonan syndrome using multiplex ligation-dependent probe amplification analysisAnna-Maja Nyström, Sara Ekvall, Ann-Charlotte Thuresson, et al.
Pediatric Dermatology|July 15, 2020
Keratinocytic epidermal nevi associated with localized fibro-osseous lesions without hypophosphatemiaLien Mestach, Satyamaanasa Polubothu, Alistair Calder, 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.
BMC Medical Genetics|September 24, 2009
Pathogenesis of vestibular schwannoma in ring chromosome 22Ellen Denayer, Hilde Brems, Paul de Cock, 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 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
European Journal of Pediatrics|July 6, 2007
What's new in the neuro-cardio-facial-cutaneous syndromes?Ellen Denayer, Eric Legius
Acta Dermato-Venereologica|March 10, 2020
Legius Syndrome and its Relationship with Neurofibromatosis Type 1Ellen Denayer, Eric Legius
Ophthalmic Genetics|May 6, 2021
Two siblings with Heimler syndrome caused by PEX1 variants: follow-up of ophthalmologic findingsDorien Herijgers, Ellen Denayer, Irina Balikova, et al.
Journal of Medical Genetics|November 23, 2025
ACTH-secreting atypical carcinoid lung tumour expanding the Lynch syndrome spectrumKevin Van Compernolle, Jacques Van Huysse, Kathleen B M Claes, et al.
European Journal of Medical Genetics|March 23, 2010
Investigation of gene dosage imbalances in patients with Noonan syndrome using multiplex ligation-dependent probe amplification analysisAnna-Maja Nyström, Sara Ekvall, Ann-Charlotte Thuresson, et al.
Pediatric Dermatology|July 15, 2020
Keratinocytic epidermal nevi associated with localized fibro-osseous lesions without hypophosphatemiaLien Mestach, Satyamaanasa Polubothu, Alistair Calder, 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.
BMC Medical Genetics|September 24, 2009
Pathogenesis of vestibular schwannoma in ring chromosome 22Ellen Denayer, Hilde Brems, Paul de Cock, 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.
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