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Genotypic and phenotypic spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency.
Goetz, M; Schröter, J; Dattner, T; Brennenstuhl, H; Lenz, D; Opladen, T; Hörster, F; Okun, J G; Hoffmann, G F; Kölker, S; Staufner, C.
Afiliação
  • Goetz M; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Schröter J; Division of Pediatric Epileptology, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Dattner T; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Brennenstuhl H; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Lenz D; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Opladen T; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Hörster F; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Okun JG; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Hoffmann GF; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Kölker S; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Staufner C; Division of Child Neurology and Metabolic Disorders, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.. Electronic address: christian.staufner@med.uni-heidelberg.de.
Mol Genet Metab ; 137(1-2): 18-25, 2022.
Article em En | MEDLINE | ID: mdl-35868242
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glutamina / Hipoglicemia Tipo de estudo: Prognostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Mol Genet Metab Ano de publicação: 2022 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: Glutamina / Hipoglicemia Tipo de estudo: Prognostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Mol Genet Metab Ano de publicação: 2022 Tipo de documento: Article