Circulating 4-F4t-Neuroprostane and 10-F4t-Neuroprostane Are Related to MECP2 Gene Mutation and Natural History in Rett Syndrome.

Signorini, Cinzia; Leoncini, Silvia; Durand, Thierry; Galano, Jean-Marie; Guy, Alexandre; Bultel-Poncé, Valérie; Oger, Camille; Lee, Jetty Chung-Yung; Ciccoli, Lucia; Hayek, Joussef; De Felice, Claudio

Circulating 4-F_4t-Neuroprostane and 10-F_4t-Neuroprostane Are Related to MECP2 Gene Mutation and Natural History in Rett Syndrome.

Signorini, Cinzia; Leoncini, Silvia; Durand, Thierry; Galano, Jean-Marie; Guy, Alexandre; Bultel-Poncé, Valérie; Oger, Camille; Lee, Jetty Chung-Yung; Ciccoli, Lucia; Hayek, Joussef; De Felice, Claudio.

Afiliação

Signorini C; Department of Molecular and Developmental Medicine, University of Siena, 53100 Siena, Italy;ciccolil@yahoo.it.
Leoncini S; Neonatal Intensive Care Unit, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy;s.leoncini74@gmail.com.
Durand T; Child Neuropsychiatry Unit, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy;hayekjoussef@gmail.com.
Galano JM; Institut des Biomolécules Max Mousseron, (IBMM), UMR 5247, CNRS, Université de Montpellier, ENSCM, CEDEX 5, 34093 Montpellier, France.
Guy A; Institut des Biomolécules Max Mousseron, (IBMM), UMR 5247, CNRS, Université de Montpellier, ENSCM, CEDEX 5, 34093 Montpellier, France.
Bultel-Poncé V; Institut des Biomolécules Max Mousseron, (IBMM), UMR 5247, CNRS, Université de Montpellier, ENSCM, CEDEX 5, 34093 Montpellier, France.
Oger C; Institut des Biomolécules Max Mousseron, (IBMM), UMR 5247, CNRS, Université de Montpellier, ENSCM, CEDEX 5, 34093 Montpellier, France.
Lee JC; Institut des Biomolécules Max Mousseron, (IBMM), UMR 5247, CNRS, Université de Montpellier, ENSCM, CEDEX 5, 34093 Montpellier, France.
Ciccoli L; School of Biological Sciences, The University of Hong Kong, Hong Kong.
Hayek J; Department of Molecular and Developmental Medicine, University of Siena, 53100 Siena, Italy;ciccolil@yahoo.it.
De Felice C; Child Neuropsychiatry Unit, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy;hayekjoussef@gmail.com.

Int J Mol Sci ; 22(8)2021 Apr 19.

Article em En | MEDLINE | ID: mdl-33921863

Assuntos

Proteína 2 de Ligação a Metil-CpG/genética; Neuroprostanos/sangue; Síndrome de Rett/sangue; Adolescente; Adulto; Criança; Pré-Escolar; Feminino; Humanos; Masculino; Pessoa de Meia-Idade; Mutação; Doenças do Sistema Nervoso/sangue; Doenças do Sistema Nervoso/genética; Síndrome de Rett/genética; Síndrome de Rett/patologia; Adulto Jovem

Palavras-chave

MECP2 mutation; Rett syndrome; natural history; neurological disease; neuroprostanes; phenotype

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Rett / Proteína 2 de Ligação a Metil-CpG / Neuroprostanos Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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