Хайлтын үр дүнгүүд - André B. P. Kuilenburg

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  1. 1
    Genotypes Affecting the Pharmacokinetics of Anticancer Drugs

    Genotypes Affecting the Pharmacokinetics of Anticancer Drugs -н Daphne Bertholee, Jan Gerard Maring, André B. P. Kuilenburg

    Хэвлэсэн 2016
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  2. 2
    Increased risk of grade IV neutropenia after administration of 5‐fluorouracil due to a dihydropyrimidine dehydrogenase deficiency: High prevalence of the IVS14+1g>a mutation

    Increased risk of grade IV neutropenia after administration of 5‐fluorouracil due to a dihydropyrimidine dehydrogenase deficiency: High prevalence of the IVS14+1g>a mutation -н André B. P. Kuilenburg, Rutger Meinsma, Lida Zoetekouw, Albert H. Gennip

    Хэвлэсэн 2002
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    Artigo
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  3. 3
    Inborn errors of pyrimidine degradation: Clinical, biochemical and molecular aspects

    Inborn errors of pyrimidine degradation: Clinical, biochemical and molecular aspects -н Albert H. Gennip, N. G. G. M. Abeling, P. Vreken, André B. P. Kuilenburg

    Хэвлэсэн 1997
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  4. 4
    Developments in the treatment of Fabry disease

    Developments in the treatment of Fabry disease -н Sanne J. van der Veen, Carla E. M. Hollak, André B. P. Kuilenburg, Mirjam Langeveld

    Хэвлэсэн 2020
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  5. 5
    Pitfalls in the Diagnosis of Patients with a Partial Dihydropyrimidine Dehydrogenase Deficiency

    Pitfalls in the Diagnosis of Patients with a Partial Dihydropyrimidine Dehydrogenase Deficiency -н André B. P. Kuilenburg, Henk van Lenthe, A. Tromp, P C Veltman, A. H. van Gennip

    Хэвлэсэн 2000
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    Artigo
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  6. 6
    Histone deacetylases (HDACs): characterization of the classical HDAC family

    Histone deacetylases (HDACs): characterization of the classical HDAC family -н Annemieke J.M. de Ruijter, Albert H. Gennip, Huib N. Caron, Stephan Kemp, André B. P. Kuilenburg

    Хэвлэсэн 2003
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  7. 7
    Acute Aerobic Exercise Leads to Increased Plasma Levels of R- and S-β-Aminoisobutyric Acid in Humans

    Acute Aerobic Exercise Leads to Increased Plasma Levels of R- and S-β-Aminoisobutyric Acid in Humans -н Jan Stautemas, André B. P. Kuilenburg, Lida Stroomer, Frédéric M. Vaz, Laura Blancquaert, Filip Lefevere, Inge Everaert, Wim Derave

    Хэвлэсэн 2019
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  8. 8
    Rapid Screening of High-Risk Patients for Disorders of Purine and Pyrimidine Metabolism Using HPLC-Electrospray Tandem Mass Spectrometry of Liquid Urine or Urine-soaked Filter Paper Strips

    Rapid Screening of High-Risk Patients for Disorders of Purine and Pyrimidine Metabolism Using HPLC-Electrospray Tandem Mass Spectrometry of Liquid Urine or Urine-soaked Filter Pape... -н Tetsuya Ito, André B. P. Kuilenburg, Albert H. Bootsma, Anja J Haasnoot, Arno van Cruchten, Yoshiro Wada, Albert H. Gennip

    Хэвлэсэн 2000
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  9. 9
    Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity

    Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity -н André B. P. Kuilenburg, P. Vreken, L.V.A.M. Beex, Rutger Meinsma, Henk van Lenthe, Ronney A. De Abreu, Albert H. Gennip

    Хэвлэсэн 1997
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  10. 10
    Long-Term Dose-Dependent Agalsidase Effects on Kidney Histology in Fabry Disease

    Long-Term Dose-Dependent Agalsidase Effects on Kidney Histology in Fabry Disease -н Rannveig Skrunes, Camilla Tøndel, Sabine Leh, Kristin Kampevold Larsen, Gunnar Houge, Einar Skulstad Davidsen, Carla E. M. Hollak, André B. P. Kuilenburg, Frédéric M. Vaz, Einar Svarstad

    Хэвлэсэн 2017
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  11. 11
    Retrospective study of long-term outcomes of enzyme replacement therapy in Fabry disease: Analysis of prognostic factors

    Retrospective study of long-term outcomes of enzyme replacement therapy in Fabry disease: Analysis of prognostic factors -н Maarten Arends, Marieke Biegstraaten, Derralynn Hughes, Atul Mehta, Perry Elliott, Daniel Oder, Oliver Watkinson, Frédéric M. Vaz, André B. P. Kuilenburg, Christoph Wanner, Carla E. M. Hollak

    Хэвлэсэн 2017
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  12. 12
    Reduced 5-FU clearance in a patient with low DPD activity due to heterozygosity for a mutant allele of the DPYD gene

    Reduced 5-FU clearance in a patient with low DPD activity due to heterozygosity for a mutant allele of the DPYD gene -н Jan Gerard Maring, André B. P. Kuilenburg, Janet Haasjes, Harry L. Piersma, Harry J.M. Groen, Donald R. A. Uges, Albert H. Gennip, Elisabeth G.E. de Vries

    Хэвлэсэн 2002
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  13. 13
    X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation

    X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation -н Matthis Synofzik, Jennifer Müller vom Hagen, Tobias B. Haack, Christian Wilhelm, Tobias Lindig, Stefanie Beck‐Wödl, Sander B. Nabuurs, André B. P. Kuilenburg, Arjan PM de Brouwer, Lüdger Schöls

    Хэвлэсэн 2014
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    Artigo
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  14. 14
    Report of Two Never Treated Adult Sisters with Aromatic l-Amino Acid Decarboxylase Deficiency: A Portrait of the Natural History of the Disease or an Expanding Phenotype?

    Report of Two Never Treated Adult Sisters with Aromatic l-Amino Acid Decarboxylase Deficiency: A Portrait of the Natural History of the Disease or an Expanding Phenotype? -н Vincenzo Leuzzi, Mario Mastrangelo, Agata Polizzi, Cristiana Artiola, André B. P. Kuilenburg, Carla Carducci, Martino Ruggieri, Rita Barone, Barbara Tavazzi, N. G. G. M. Abeling, Lida Zoetekouw, Vito Sofia, Mario Zappia, Claudia Carducci

    Хэвлэсэн 2014
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  15. 15
    Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjects

    Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjects -н Susan A. Ridge, Julieann Sludden, Oliver E. Brown, Leigh Robertson, Xiaoxiong Wei, Andrea Sapone, Pedro M. Fernández‐Salguero, Frank J. Gonzalez, P. Vreken, André B. P. Kuilenburg, Albert H. Gennip, Howard L. McLeod

    Хэвлэсэн 1998
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  16. 16
    Predicting the Development of Anti-Drug Antibodies against Recombinant alpha-Galactosidase A in Male Patients with Classical Fabry Disease

    Predicting the Development of Anti-Drug Antibodies against Recombinant alpha-Galactosidase A in Male Patients with Classical Fabry Disease -н Sanne J. van der Veen, Wytze J. Vlietstra, Laura van Dussen, André B. P. Kuilenburg, Marcel G. W. Dijkgraaf, Malte Lenders, Eva Brand, Christoph Wanner, Derralynn Hughes, Perry Elliott, Carla E. M. Hollak, Mirjam Langeveld

    Хэвлэсэн 2020
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  17. 17
    De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise

    De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise -н Karin Writzl, Aleš Maver, Lidija Kovačič, Paula Martínez-Valero, Laura Contreras, Jorgina Satrústegui, Marco Castori, Laurence Bonhomme‐Faivre, Pablo Lapunzina, André B. P. Kuilenburg, Slobodanka Radović, Christel Thauvin‐Robinet, Borut Peterlin, Araceli del Arco, Raoul C. M. Hennekam

    Хэвлэсэн 2017
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  18. 18
    Multi-OMIC profiling of survival and metabolic signaling networks in cells subjected to photodynamic therapy

    Multi-OMIC profiling of survival and metabolic signaling networks in cells subjected to photodynamic therapy -н Ruud Weijer, Séverine Clavier, Esther A. Zaal, Maud M. E. Pijls, Robert T. van Kooten, Klaas Vermaas, René Leen, Aldo Jongejan, Perry D. Moerland, Antoine H. C. van Kampen, André B. P. Kuilenburg, Celia R. Berkers, Simone Lemeer, Michal Heger

    Хэвлэсэн 2016
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  19. 19
    Agalsidase alfa versus agalsidase beta for the treatment of Fabry disease: an international cohort study

    Agalsidase alfa versus agalsidase beta for the treatment of Fabry disease: an international cohort study -н Maarten Arends, Marieke Biegstraaten, Christoph Wanner, Sandra Sirrs, Atul Mehta, Perry Elliott, Daniel Oder, Oliver Watkinson, Daniel G. Bichet, Anzalee Khan, Mark Iwanochko, Frédéric M. Vaz, André B. P. Kuilenburg, Michael L. West, Derralynn Hughes, Carla E. M. Hollak

    Хэвлэсэн 2018
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  20. 20
    Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure

    Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure -н André B. P. Kuilenburg, Doreen Dobritzsch, Rutger Meinsma, Janet Haasjes, Hans R. Waterham, Małgorzata J.M. Nowaczyk, George Maropoulos, Guido Hein, Hermann Kalhoff, J M Kirk, Holger BAASKE, Anne Aukett, John A. Duley, K. P. Ward, Ylva Lindqvist, Albert H. Gennip

    Хэвлэсэн 2002
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