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Baclofen-associated neurophysiologic target engagement across species in fragile X syndrome.
Jonak, Carrie R; Pedapati, Ernest V; Schmitt, Lauren M; Assad, Samantha A; Sandhu, Manbir S; DeStefano, Lisa; Ethridge, Lauren; Razak, Khaleel A; Sweeney, John A; Binder, Devin K; Erickson, Craig A.
Afiliación
  • Jonak CR; Division of Biomedical Sciences, School of Medicine, University of California, Riverside, USA.
  • Pedapati EV; Division of Child and Adolescent Psychiatry, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Schmitt LM; Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Assad SA; Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Sandhu MS; Division of Developmental and Behavioral Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • DeStefano L; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Ethridge L; Division of Biomedical Sciences, School of Medicine, University of California, Riverside, USA.
  • Razak KA; Division of Biomedical Sciences, School of Medicine, University of California, Riverside, USA.
  • Sweeney JA; Division of Child and Adolescent Psychiatry, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Binder DK; Department of Psychology, University of Oklahoma, Norman, OK, USA.
  • Erickson CA; Department of Psychology, University of Oklahoma, Norman, OK, USA.
J Neurodev Disord ; 14(1): 52, 2022 09 27.
Article en En | MEDLINE | ID: mdl-36167501
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome del Cromosoma X Frágil Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans / Male Idioma: En Revista: J Neurodev Disord Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome del Cromosoma X Frágil Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans / Male Idioma: En Revista: J Neurodev Disord Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos