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Intrathecal magnesium delivery for Mg++-insensitive NMDA receptor activity due to GRIN1 mutation.
Lewis, Sara A; Shetty, Sheetal; Gamble, Sean; Heim, Jennifer; Zhao, Ningning; Stitt, Gideon; Pankratz, Matthew; Mangum, Tara; Marku, Iris; Rosenberg, Robert B; Wilfong, Angus A; Fahey, Michael C; Kim, Sukhan; Myers, Scott J; Appavu, Brian; Kruer, Michael C.
Afiliação
  • Lewis SA; Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, 85016, USA.
  • Shetty S; Departments of Child Health, Neurology, Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, AZ, USA.
  • Gamble S; Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, 85016, USA.
  • Heim J; Departments of Child Health, Neurology, Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, AZ, USA.
  • Zhao N; Valley Anesthesia, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Stitt G; Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, 85016, USA.
  • Pankratz M; Department of Nutritional Sciences, University of Arizona, Tucson, AZ, USA.
  • Mangum T; Department of Pharmacy & Therapeutics, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Marku I; Phoenix Children's Hospital Biorepository, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Rosenberg RB; Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, 85016, USA.
  • Wilfong AA; Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, 85016, USA.
  • Fahey MC; Division of Pediatric Critical Care Medicine, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Kim S; Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, 85016, USA.
  • Myers SJ; Departments of Paediatrics and Neurology, Monash University, Melbourne, VIC, Australia.
  • Appavu B; Center for Functional Evaluation of Rare Variants, Emory University, Atlanta, GA, USA.
  • Kruer MC; Center for Functional Evaluation of Rare Variants, Emory University, Atlanta, GA, USA.
Orphanet J Rare Dis ; 18(1): 225, 2023 08 03.
Article em En | MEDLINE | ID: mdl-37537625
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Magnésio / Deficiência Intelectual Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Magnésio / Deficiência Intelectual Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2023 Tipo de documento: Article