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Proposal for an individualized dietary strategy in patients with very long-chain acyl-CoA dehydrogenase deficiency.
Bleeker, Jeannette C; Kok, Irene L; Ferdinandusse, Sacha; de Vries, Maaike; Derks, Terry G J; Mulder, Margot F; Williams, Monique; Gozalbo, Estela Rubio; Bosch, Annet M; van den Hurk, Dorine T; de Sain-van der Velden, Monique G M; Waterham, Hans R; Wijburg, Frits A; Visser, Gepke.
Afiliación
  • Bleeker JC; Department of Metabolic Diseases, Dutch Fatty Acid Oxidation Expertise Center, Wilhelmina Children's Hospital (UMCU), University Medical Center Utrecht, Internal Mail KE 04.306.0, PO Box 85090 3508 AB, Utrecht, Netherlands.
  • Kok IL; Laboratory Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, Netherlands.
  • Ferdinandusse S; Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands.
  • de Vries M; Department of Metabolic Diseases, Dutch Fatty Acid Oxidation Expertise Center, Wilhelmina Children's Hospital (UMCU), University Medical Center Utrecht, Internal Mail KE 04.306.0, PO Box 85090 3508 AB, Utrecht, Netherlands.
  • Derks TGJ; Department of Internal Medicine and Dermatology, Dietetics, University Medical Center Utrecht, Utrecht, Netherlands.
  • Mulder MF; Laboratory Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, Netherlands.
  • Williams M; Department of Pediatrics, Radboud University Medical Center, Nijmegen, Netherlands.
  • Gozalbo ER; Department of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, Groningen, Netherlands.
  • Bosch AM; Department of Pediatrics, VU University Medical Center Amsterdam, Amsterdam, Netherlands.
  • van den Hurk DT; Department of Pediatrics, Erasmus MC-Sophia, Rotterdam, Netherlands.
  • de Sain-van der Velden MGM; Department of Pediatrics and Laboratory Genetic Metabolic Diseases, Maastricht University Medical Center, Maastricht, Netherlands.
  • Waterham HR; Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands.
  • Wijburg FA; Department of Internal Medicine and Dermatology, Dietetics, University Medical Center Utrecht, Utrecht, Netherlands.
  • Visser G; Department of Medical Genetics, Section Metabolic Diagnostics, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, Netherlands.
J Inherit Metab Dis ; 42(1): 159-168, 2019 01.
Article en En | MEDLINE | ID: mdl-30740737
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Acil-CoA Deshidrogenasa / Acil-CoA Deshidrogenasa de Cadena Larga / Síndromes Congénitos de Insuficiencia de la Médula Ósea / Errores Innatos del Metabolismo Lipídico / Enfermedades Musculares Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male / Newborn Idioma: En Revista: J Inherit Metab Dis Año: 2019 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Acil-CoA Deshidrogenasa / Acil-CoA Deshidrogenasa de Cadena Larga / Síndromes Congénitos de Insuficiencia de la Médula Ósea / Errores Innatos del Metabolismo Lipídico / Enfermedades Musculares Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male / Newborn Idioma: En Revista: J Inherit Metab Dis Año: 2019 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Estados Unidos