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Laurent Guibaud

Showing results (51-60 of 109) with videos related to

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Fluids and Barriers of the CNS|June 7, 2022
Vascular network expansion, integrity of blood-brain interfaces, and cerebrospinal fluid cytokine concentration during postnatal development in the normal and jaundiced ratSandrine Blondel, Nathalie Strazielle, Amel Amara, et al.
Neurogenetics|January 8, 2021
X-linked partial corpus callosum agenesis with mild intellectual disability: identification of a novel L1CAM pathogenic variantIdriss Bousquet, Muriel Bozon, Valérie Castellani, et al.
American Journal of Medical Genetics. Part A|July 28, 2017
Autopsy findings in EPG5-related Vici syndrome with antenatal onsetRenaud Touraine, Annie Laquerrière, Carmen-Adina Petcu, et al.
European Journal of Medical Genetics|December 12, 2022
Surgical management of Chiari malformation type 1 associated to MCAP syndrome and study of cerebellar and adjacent tissues for PIK3CA mosaicismFederico Di Rocco, Maria Lucia Licci, Aurore Garde, et al.
European Journal of Medical Genetics|October 28, 2006
Polymicrogyria, cerebellar vermis hypoplasia, severe facial dysmorphism and cleft palate: a new syndrome?Anne-Laure Mosca, Nicole Laurent, Laurent Guibaud, et al.
Brain : a Journal of Neurology|October 15, 2019
A novel lethal recognizable polymicrogyric syndrome caused by ATP1A2 homozygous truncating variantsNicolas Chatron, Sara Cabet, Eudeline Alix, et al.
Cells|October 15, 2025
A Pleiotropic and Functionally Divergent <i>RAC3</i> Variant Disrupts Neurodevelopment and Impacts OrganogenesisRyota Sugawara, Marcello Scala, Sara Cabet, et al.
Prenatal Diagnosis|February 20, 2026
Prenatal Diagnosis and Neurodevelopmental Outcome of Children With Marked Opening of the Fourth Ventricle: Challenges and Pitfalls in MRI Diagnostic CriteriaLéa Schieffer, Catherine Garel, Laurent Guibaud, et al.
American Journal of Medical Genetics. Part A|February 5, 2017
A novel disorder of sex development, characterized by progressive regression of testicular function and cystic leukoencephalopathyMassimiliano Rossi, Alexandre Vasiljevic, Audrey Labalme, et al.
Prenatal Diagnosis|May 16, 2026
Prenatal Diagnosis and Management of Kaposiform Hemangioendothelioma With Kasabach-Merritt Phenomenon: Imaging Features and First Experience With Maternal Sirolimus TherapyAntoine Fraissenon, Chris Minella, Marion Bordas-Fournel, et al.
Pageof 11

Showing results (51-60 of 109) with videos related to

Sort By:
Pageof 11
Fluids and Barriers of the CNS|June 7, 2022
Vascular network expansion, integrity of blood-brain interfaces, and cerebrospinal fluid cytokine concentration during postnatal development in the normal and jaundiced ratSandrine Blondel, Nathalie Strazielle, Amel Amara, et al.
Neurogenetics|January 8, 2021
X-linked partial corpus callosum agenesis with mild intellectual disability: identification of a novel L1CAM pathogenic variantIdriss Bousquet, Muriel Bozon, Valérie Castellani, et al.
American Journal of Medical Genetics. Part A|July 28, 2017
Autopsy findings in EPG5-related Vici syndrome with antenatal onsetRenaud Touraine, Annie Laquerrière, Carmen-Adina Petcu, et al.
European Journal of Medical Genetics|December 12, 2022
Surgical management of Chiari malformation type 1 associated to MCAP syndrome and study of cerebellar and adjacent tissues for PIK3CA mosaicismFederico Di Rocco, Maria Lucia Licci, Aurore Garde, et al.
European Journal of Medical Genetics|October 28, 2006
Polymicrogyria, cerebellar vermis hypoplasia, severe facial dysmorphism and cleft palate: a new syndrome?Anne-Laure Mosca, Nicole Laurent, Laurent Guibaud, et al.
Brain : a Journal of Neurology|October 15, 2019
A novel lethal recognizable polymicrogyric syndrome caused by ATP1A2 homozygous truncating variantsNicolas Chatron, Sara Cabet, Eudeline Alix, et al.
Cells|October 15, 2025
A Pleiotropic and Functionally Divergent <i>RAC3</i> Variant Disrupts Neurodevelopment and Impacts OrganogenesisRyota Sugawara, Marcello Scala, Sara Cabet, et al.
Prenatal Diagnosis|February 20, 2026
Prenatal Diagnosis and Neurodevelopmental Outcome of Children With Marked Opening of the Fourth Ventricle: Challenges and Pitfalls in MRI Diagnostic CriteriaLéa Schieffer, Catherine Garel, Laurent Guibaud, et al.
American Journal of Medical Genetics. Part A|February 5, 2017
A novel disorder of sex development, characterized by progressive regression of testicular function and cystic leukoencephalopathyMassimiliano Rossi, Alexandre Vasiljevic, Audrey Labalme, et al.
Prenatal Diagnosis|May 16, 2026
Prenatal Diagnosis and Management of Kaposiform Hemangioendothelioma With Kasabach-Merritt Phenomenon: Imaging Features and First Experience With Maternal Sirolimus TherapyAntoine Fraissenon, Chris Minella, Marion Bordas-Fournel, et al.
Pageof 11