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Multimodal assessment of the GABA system in patients with fragile-X syndrome and neurofibromatosis of type 1.
Lacroix, Angelina; Proteau-Lemieux, Mélodie; Côté, Samantha; Near, Jamie; Hui, Steve C N; Edden, Richard A E; Lippé, Sarah; Çaku, Artuela; Corbin, François; Lepage, Jean-François.
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  • Lacroix A; Sherbrooke University Hospital Research Center, Sherbrooke, Canada.
  • Proteau-Lemieux M; Sherbrooke University Hospital Research Center, Sherbrooke, Canada.
  • Côté S; Sherbrooke University Hospital Research Center, Sherbrooke, Canada.
  • Near J; University of Toronto, Medical Biophysics and Physical Sciences Platform at Sunnybrook Research Institute, Toronto, Canada.
  • Hui SCN; Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD, USA.
  • Edden RAE; Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD, USA.
  • Lippé S; Department of Psychology, Faculty of Arts and Sciences, Université de Montréal, Montréal, Canada.
  • Çaku A; Sherbrooke University Hospital Research Center, Sherbrooke, Canada; Department of Biochemistry, Faculty of Medicine and Health Sciences, Sherbrooke University, Sherbrooke, Canada.
  • Corbin F; Sherbrooke University Hospital Research Center, Sherbrooke, Canada; Department of Biochemistry, Faculty of Medicine and Health Sciences, Sherbrooke University, Sherbrooke, Canada.
  • Lepage JF; Sherbrooke University Hospital Research Center, Sherbrooke, Canada; Departments of Pediatrics, Faculty of Medicine and Health Sciences, Sherbrooke University, Sherbrooke, Canada. Electronic address: jean-francois.lepage@usherbrooke.ca.
Neurobiol Dis ; 174: 105881, 2022 Nov.
Article en En | MEDLINE | ID: mdl-36202290
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neurofibromatosis 1 / Síndrome del Cromosoma X Frágil / Corteza Motora Idioma: En Revista: Neurobiol Dis Año: 2022 Tipo del documento: Article País de afiliación: Canadá
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neurofibromatosis 1 / Síndrome del Cromosoma X Frágil / Corteza Motora Idioma: En Revista: Neurobiol Dis Año: 2022 Tipo del documento: Article País de afiliación: Canadá