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Evaluation of QTc in Rett syndrome: Correlation with age, severity, and genotype.
Crosson, Jane; Srivastava, Siddharth; Bibat, Genila M; Gupta, Siddharth; Kantipuly, Aditi; Smith-Hicks, Constance; Myers, Scott M; Sanyal, Abanti; Yenokyan, Gayane; Brenner, Joel; Naidu, Sakkubai R.
Afiliação
  • Crosson J; Division of Pediatric Cardiology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Srivastava S; Department of Neurology, Boston Children's Hospital, Boston, Massachusetts.
  • Bibat GM; Department of Neurogenetics, Kennedy Krieger Institute, Baltimore, Maryland.
  • Gupta S; Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, Maryland.
  • Kantipuly A; Department of Neurogenetics, Kennedy Krieger Institute, Baltimore, Maryland.
  • Smith-Hicks C; Department of Neurogenetics, Kennedy Krieger Institute, Baltimore, Maryland.
  • Myers SM; Department of Neurogenetics, Kennedy Krieger Institute, Baltimore, Maryland.
  • Sanyal A; Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, Maryland.
  • Yenokyan G; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Brenner J; Autism & Developmental Institute, Geisinger Health System, Lewisburg, Pennsylvania.
  • Naidu SR; Johns Hopkins Biostatistics Center, Department of Biostatistics, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland.
Am J Med Genet A ; 173(6): 1495-1501, 2017 Jun.
Article em En | MEDLINE | ID: mdl-28394409
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Rett / Morte Súbita Cardíaca / Eletrocardiografia / Proteína 2 de Ligação a Metil-CpG Tipo de estudo: Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Rett / Morte Súbita Cardíaca / Eletrocardiografia / Proteína 2 de Ligação a Metil-CpG Tipo de estudo: Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de publicação: Estados Unidos