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Autism spectrum disorders in propionic acidemia patients.
de la Bâtie, Caroline Dejean; Barbier, Valérie; Roda, Célina; Brassier, Anaïs; Arnoux, Jean-Baptiste; Valayannopoulos, Vassili; Guemann, Anne-Sophie; Pontoizeau, Clément; Gobin, Stéphanie; Habarou, Florence; Lacaille, Florence; Bonnefont, Jean-Paul; Canouï, Pierre; Ottolenghi, Chris; De Lonlay, Pascale; Ouss, Lisa.
Afiliação
  • de la Bâtie CD; Service de Pédopsychiatrie, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, 149 rue de Sèvres, 75015, Paris, France.
  • Barbier V; Reference Center of Inherited Metabolic Diseases, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Roda C; Reference Center of Inherited Metabolic Diseases, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Brassier A; Reference Center of Inherited Metabolic Diseases, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Arnoux JB; Reference Center of Inherited Metabolic Diseases, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Valayannopoulos V; Reference Center of Inherited Metabolic Diseases, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Guemann AS; Reference Center of Inherited Metabolic Diseases, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Pontoizeau C; Service de Biochimie Métabolique, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Gobin S; Service de Génétique, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Habarou F; Service de Biochimie Métabolique, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Lacaille F; Service de Gastro-entérologie et hépatologie, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Bonnefont JP; Service de Génétique, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Canouï P; Service de Pédopsychiatrie, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, 149 rue de Sèvres, 75015, Paris, France.
  • Ottolenghi C; Service de Biochimie Métabolique, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • De Lonlay P; Reference Center of Inherited Metabolic Diseases, Imagine Institute, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, Paris, France.
  • Ouss L; Service de Pédopsychiatrie, Hôpital Necker-Enfants Malades, Université Paris Descartes, APHP, 149 rue de Sèvres, 75015, Paris, France. lisa.ouss@aphp.fr.
J Inherit Metab Dis ; 41(4): 623-629, 2018 07.
Article em En | MEDLINE | ID: mdl-28856627
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Acidemia Propiônica / Transtorno do Espectro Autista Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Acidemia Propiônica / Transtorno do Espectro Autista Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França