Search Results - Marinus Durán

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  1. 1
    Enzymology of the branched‐chain amino acid oxidation disorders: the valine pathway

    Enzymology of the branched‐chain amino acid oxidation disorders: the valine pathway by Ronald J. A. Wanders, Marinus Durán, Ference J. Loupatty

    Published 2010
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  2. 2
    Dynamic Changes of Plasma Acylcarnitine Levels Induced by Fasting and Sunflower Oil Challenge Test in Children

    Dynamic Changes of Plasma Acylcarnitine Levels Induced by Fasting and Sunflower Oil Challenge Test in Children by Catarina C G Costa, Isabel Tavares de Almeida, Cornelis Jakobs, Bwee Tien Poll‐The, Marinus Duran

    Published 1999
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  3. 3
    l-Serine in disease and development

    l-Serine in disease and development by Tom J. de Koning, Keith Snell, Marinus Durán, Ruud Berger, Bwee Tien Poll‐The, Robert Surtees

    Published 2003
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  4. 4
    Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid β-oxidation disorders

    Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid β-oxidation disorders by Catarina G. Costa, L. Dorland, U. Holwerda, Isabel Tavares de Almeida, Bwee Tien Poll‐The, Cornelis Jakobs, Marinus Durán

    Published 1998
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  5. 5
    Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase

    Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase by R. B. H. Schutgens, H. S. A. Heymans, Arnold Ketel, H.A. Veder, Marinus Durán, D. Ketting, S.K. Wadman

    Published 1979
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  6. 6
    Familial Hyperinsulinemic Hypoglycemia Caused by a Defect in the SCHAD Enzyme of Mitochondrial Fatty Acid Oxidation

    Familial Hyperinsulinemic Hypoglycemia Caused by a Defect in the SCHAD Enzyme of Mitochondrial Fatty Acid Oxidation by Anders Molven, Guri E. Matre, Marinus Durán, Ronald J. A. Wanders, U Rishaug, Pål R. Njølstad, Egil Jellum, Oddmund Søvik

    Published 2004
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  7. 7
    Muscle acylcarnitines during short-term fasting in lean healthy men

    Muscle acylcarnitines during short-term fasting in lean healthy men by Maarten R. Soeters, Hans P. Sauerwein, Marinus Durán, Ronald J. A. Wanders, Mariëtte T. Ackermans, Eric Fliers, Sander M. Houten, Mireille J. Serlie

    Published 2008
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  8. 8
    Plasma and Erythrocyte Fatty Acid Patterns in Patients with Recurrent Depression: A Matched Case-Control Study

    Plasma and Erythrocyte Fatty Acid Patterns in Patients with Recurrent Depression: A Matched Case-Control Study by Johanna Assies, Frans Pouwer, Anja Lok, Roel J. T. Mocking, Claudi Bockting, Ieke Visser, N. G. G. M. Abeling, Marinus Durán, Aart H. Schene

    Published 2010
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  9. 9
    Alkyl-Glycerol Rescues Plasmalogen Levels and Pathology of Ether-Phospholipid Deficient Mice

    Alkyl-Glycerol Rescues Plasmalogen Levels and Pathology of Ether-Phospholipid Deficient Mice by Pedro Brites, Ana S. Ferreira, Tiago Ferreira da Silva, Vera Sousa, Ana Rita Malheiro, Marinus Durán, Hans R. Waterham, Myriam Baes, Ronald J. A. Wanders

    Published 2011
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  10. 10
    Beneficial effects of <scp>L</scp>‐serine and glycine in the management of seizures in 3‐phosphoglycerate dehydrogenase deficiency

    Beneficial effects of <scp>L</scp>‐serine and glycine in the management of seizures in 3‐phosphoglycerate dehydrogenase deficiency by Tom J. de Koning, Marinus Durán, L. Dorland, R. H. J. M. Gooskens, Emile Van Schaftingen, Jaak Jaeken, Nenad Blau, Ruud Berger, Bwee Tien Poll‐The

    Published 1998
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  11. 11
    Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis

    Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis by C. C. P. Aires, Lodewijk IJlst, Femke S. Stet, Carina Prip‐Buus, Isabel Tavares de Almeida, Marinus Durán, Ronald J. A. Wanders, M. F. B. Silva

    Published 2009
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  12. 12
    2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency Is Caused by Mutations in the HADH2 Gene

    2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency Is Caused by Mutations in the HADH2 Gene by Rob Ofman, P.N. Jos Ruiter, Marike Feenstra, Marinus Durán, Bwee Tien Poll‐The, Johannes Zschocke, Regina Ensenauer, W. Lehnert, Jörn Oliver Sass, Wolfgang Sperl, Jennifer Wanders

    Published 2003
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  13. 13
    Low-dose folic acid supplementation decreases plasma homocysteine concentrations: a randomized trial

    Low-dose folic acid supplementation decreases plasma homocysteine concentrations: a randomized trial by Ingeborg A. Brouwer, Marijke van Dusseldorp, Chris M.G. Thomas, Marinus Durán, J.G.A.J. Hautvast, T.K.A.B. Eskes, Régine P.M. Steegers‐Theunissen

    Published 1999
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  14. 14
    A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy

    A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy by Jan de Boer, Jan de Wit, Harry van Steeg, Rob J. W. Berg, Hans Morreau, Pim Visser, Alan R. Lehmann, Marinus Durán, Jane H.J. Hoeijmakers, Geert Weeda

    Published 1998
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  15. 15
    Substrate specificity of human carnitine acetyltransferase: Implications for fatty acid and branched-chain amino acid metabolism

    Substrate specificity of human carnitine acetyltransferase: Implications for fatty acid and branched-chain amino acid metabolism by Sara Violante, Lodewijk IJlst, Jos P.N. Ruiter, Janet Koster, Henk van Lenthe, Marinus Durán, Isabel Tavares de Almeida, Ronald J. A. Wanders, Sander M. Houten, Fátima V. Ventura

    Published 2013
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  16. 16
    Smith-Lemli-Opitz Syndrome Is Caused by Mutations in the 7-Dehydrocholesterol Reductase Gene

    Smith-Lemli-Opitz Syndrome Is Caused by Mutations in the 7-Dehydrocholesterol Reductase Gene by Hans R. Waterham, Frits A. Wijburg, Raoul C. M. Hennekam, P. Vreken, Bwee Tien Poll‐The, L. Dorland, Marinus Durán, Petr Jira, Jan Smeitink, Ron A. Wevers, Ronald J. A. Wanders

    Published 1998
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  17. 17
    Mutations in the Gene Encoding 3-Hydroxyisobutyryl-CoA Hydrolase Results in Progressive Infantile Neurodegeneration

    Mutations in the Gene Encoding 3-Hydroxyisobutyryl-CoA Hydrolase Results in Progressive Infantile Neurodegeneration by Ference J. Loupatty, Peter T. Clayton, Jos P.N. Ruiter, Rob Ofman, Lodewijk IJlst, Garry K. Brown, David R. Thorburn, Robert A. Harris, Marinus Durán, Carlos DeSousa, S. Krywawych, Simon Heales, Ronald J. A. Wanders

    Published 2006
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  18. 18
    Brown‐Vialetto‐Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment

    Brown‐Vialetto‐Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment... by Annet M. Bosch, N. G. G. M. Abeling, Lodewijk IJlst, Hennie Knoester, W. Ludo van der Pol, A. E. M. Stroomer, Ronald J. A. Wanders, Gepke Visser, Frits A. Wijburg, Marinus Durán, Hans R. Waterham

    Published 2010
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  19. 19
    Dietary Folate from Vegetables and Citrus Fruit Decreases Plasma Homocysteine Concentrations in Humans in a Dietary Controlled Trial

    Dietary Folate from Vegetables and Citrus Fruit Decreases Plasma Homocysteine Concentrations in Humans in a Dietary Controlled Trial by Ingeborg A. Brouwer, Marijke van Dusseldorp, Clive E. West, S. Meyboom, Chris M.G. Thomas, Marinus Durán, Karin H. van het Hof, T.K.A.B. Eskes, J.G.A.J. Hautvast, Régine P.M. Steegers‐Theunissen

    Published 1999
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  20. 20
    Genetic basis of alpha‐aminoadipic and alpha‐ketoadipic aciduria

    Genetic basis of alpha‐aminoadipic and alpha‐ketoadipic aciduria by Jacob Hagen, Heleen te Brinke, Ronald J. A. Wanders, Alida C. Knegt, Esmée Oussoren, A. Jeannette M. Hoogeboom, George J. G. Ruijter, Daniel M. Becker, Karl Otfried Schwab, Ingo Franke, Marinus Durán, Hans R. Waterham, Jörn Oliver Sass, Sander M. Houten

    Published 2015
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