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Multifactorial modulation of susceptibility to l-lysine in an animal model of glutaric aciduria type I.
Sauer, Sven W; Opp, Silvana; Komatsuzaki, Shoko; Blank, Anna-Eva; Mittelbronn, Michel; Burgard, Peter; Koeller, D M; Okun, Jürgen G; Kölker, Stefan.
Afiliación
  • Sauer SW; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital Heidelberg, D-69120 Heidelberg, Germany.
  • Opp S; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital Heidelberg, D-69120 Heidelberg, Germany.
  • Komatsuzaki S; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital Heidelberg, D-69120 Heidelberg, Germany.
  • Blank AE; Institute of Neurology (Edinger Institute), Goethe-University Frankfurt, D-60528 Frankfurt/Main, Germany.
  • Mittelbronn M; Institute of Neurology (Edinger Institute), Goethe-University Frankfurt, D-60528 Frankfurt/Main, Germany.
  • Burgard P; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital Heidelberg, D-69120 Heidelberg, Germany.
  • Koeller DM; Department of Pediatrics, Oregon Health and Science University, Portland, OR, USA.
  • Okun JG; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital Heidelberg, D-69120 Heidelberg, Germany.
  • Kölker S; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital Heidelberg, D-69120 Heidelberg, Germany. Electronic address: stefan.koelker@med.uni-heidelberg.de.
Biochim Biophys Acta ; 1852(5): 768-77, 2015 May.
Article en En | MEDLINE | ID: mdl-25558815

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Encefalopatías Metabólicas / Predisposición Genética a la Enfermedad / Glutaril-CoA Deshidrogenasa / Errores Innatos del Metabolismo de los Aminoácidos / Lisina Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Biochim Biophys Acta Año: 2015 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Encefalopatías Metabólicas / Predisposición Genética a la Enfermedad / Glutaril-CoA Deshidrogenasa / Errores Innatos del Metabolismo de los Aminoácidos / Lisina Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Biochim Biophys Acta Año: 2015 Tipo del documento: Article País de afiliación: Alemania