Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Laurent Guibaud

Showing results (61-70 of 109) with videos related to

Pageof 11
Sort By:
European Journal of Medical Genetics|June 30, 2006
A new case of megalencephaly and perisylvian polymicrogyria with post-axial polydactyly and hydrocephalus: MPPH syndromeMarina Colombani, Mondher Chouchane, Gaelle Pitelet, et al.
Annales De Biologie Clinique|September 28, 2018
How to manage chickenpox during pregnancy: case reportsAlexandre Gaymard, Maxime Pichon, Antonin Bal, et al.
European Journal of Medical Genetics|August 18, 2020
Compassionate use of everolimus for refractory epilepsy in a patient with MTOR mosaic mutationNawale Hadouiri, Veronique Darmency, Laurent Guibaud, et al.
European Journal of Radiology|April 5, 2011
Treatment of venous malformations: first experience with a new sclerosing agent--a multicenter studyMartin Schumacher, Patrick Dupuy, Jean-Michel Bartoli, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Mosaic 18q21.2 deletions including the TCF4 gene: a clinical reportMassimiliano Rossi, Audrey Labalme, Marie-Pierre Cordier, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
Multiple cysts of the corpus callosum and psychomotor delay in a patient with a 3.1 Mb 15q24.1q24.2 interstitial deletion identified by array-CGHAlice Masurel-Paulet, Patrick Callier, Christel Thauvin-Robinet, et al.
Virchows Archiv : an International Journal of Pathology|May 8, 2022
Identification of a novel translocation producing an in-frame fusion of TAF15 and ETV4 in a case of extraosseous Ewing sarcoma revealed in the prenatal periodCécile Picard, Nicolas Macagno, Nadège Corradini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2020
Normal intellectual skills in patients with RhombencephalosynapsisMarie-France Bonnetain, Christelle Rougeot-Jung, Catherine Sarret, et al.
Orphanet Journal of Rare Diseases|January 13, 2023
French national diagnosis and care protocol (PNDS, protocole national de diagnostic et de soins): cystic lymphatic malformationsNicolas Leboulanger, Annouk Bisdorff, Olivia Boccara, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 27, 2017
Outcome of isolated agenesis of the corpus callosum: A population-based prospective studyVincent des Portes, Anne Rolland, Juan Velazquez-Dominguez, et al.
Pageof 11

Showing results (61-70 of 109) with videos related to

Sort By:
Pageof 11
European Journal of Medical Genetics|June 30, 2006
A new case of megalencephaly and perisylvian polymicrogyria with post-axial polydactyly and hydrocephalus: MPPH syndromeMarina Colombani, Mondher Chouchane, Gaelle Pitelet, et al.
Annales De Biologie Clinique|September 28, 2018
How to manage chickenpox during pregnancy: case reportsAlexandre Gaymard, Maxime Pichon, Antonin Bal, et al.
European Journal of Medical Genetics|August 18, 2020
Compassionate use of everolimus for refractory epilepsy in a patient with MTOR mosaic mutationNawale Hadouiri, Veronique Darmency, Laurent Guibaud, et al.
European Journal of Radiology|April 5, 2011
Treatment of venous malformations: first experience with a new sclerosing agent--a multicenter studyMartin Schumacher, Patrick Dupuy, Jean-Michel Bartoli, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Mosaic 18q21.2 deletions including the TCF4 gene: a clinical reportMassimiliano Rossi, Audrey Labalme, Marie-Pierre Cordier, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
Multiple cysts of the corpus callosum and psychomotor delay in a patient with a 3.1 Mb 15q24.1q24.2 interstitial deletion identified by array-CGHAlice Masurel-Paulet, Patrick Callier, Christel Thauvin-Robinet, et al.
Virchows Archiv : an International Journal of Pathology|May 8, 2022
Identification of a novel translocation producing an in-frame fusion of TAF15 and ETV4 in a case of extraosseous Ewing sarcoma revealed in the prenatal periodCécile Picard, Nicolas Macagno, Nadège Corradini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2020
Normal intellectual skills in patients with RhombencephalosynapsisMarie-France Bonnetain, Christelle Rougeot-Jung, Catherine Sarret, et al.
Orphanet Journal of Rare Diseases|January 13, 2023
French national diagnosis and care protocol (PNDS, protocole national de diagnostic et de soins): cystic lymphatic malformationsNicolas Leboulanger, Annouk Bisdorff, Olivia Boccara, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 27, 2017
Outcome of isolated agenesis of the corpus callosum: A population-based prospective studyVincent des Portes, Anne Rolland, Juan Velazquez-Dominguez, et al.
Pageof 11