Antibodies against recombinant enzyme in the treatment of Fabry disease: Now you see them, now you don’t by Sanne Jolien van der Veen, Mirjam Langeveld

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Recurrent metabolic alkalosis following ketone body treatment of adult mitochondrial trifunctional protein deficiency: A case report by Nina N. Stolwijk, Mirjam Langeveld, Bart A. W. Jacobs, Liffert Vogt, Jorien A. Haverkamp, Sacha Ferdinandusse, Carla E. M. Hollak

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A qualitative study on the perspectives of mothers who had been diagnosed with primary carnitine deficiency through newborn screening of their child by Lieke M. van den Heuvel, Adriana Kater-Kuipers, Tessa van Dijk, Loek L. Crefcoeur, Gepke Visser, Mirjam Langeveld, Lidewij Henneman

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The Mini Mental State Examination does not accurately screen for objective cognitive impairment in Fabry Disease by Simon Körver, Sara A. J. van deSchraaf, Gert J. Geurtsen, Carla E. M. Hollak, Ivo N. vanSchaik, Mirjam Langeveld

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Expanding Neonatal Bloodspot Screening: A Multi-Stakeholder Perspective by Tessa van Dijk, Adriana Kater, Marleen Jansen, Wybo J. Dondorp, Maartje Blom, Stephan Kemp, Mirjam Langeveld, Martina C. Cornel, Sylvia M. van der Pal, Lidewij Henneman

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Depressive symptoms in Fabry disease: the importance of coping, subjective health perception and pain by Simon Körver, Gert J. Geurtsen, Carla E. M. Hollak, Ivo N. van Schaik, Maria G. F. Longo, Marjana R. Lima, Leonardo Vedolin, Marcel G. W. Dijkgraaf, Mirjam Langeveld

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Patients’ view on gene therapy development for lysosomal storage disorders: a qualitative study by Eline C. B. Eskes, Cathrien R. L. Beishuizen, Eleonore M. Corazolla, Tessa van Middelaar, Marion M. M. G. Brands, Hanka Dekker, Erica van de Mheen, Mirjam Langeveld, Carla E. M. Hollak, Barbara Sjouke

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ECG Changes during Adult Life in Fabry Disease: Results from a Large Longitudinal Cohort Study by Mohamed El Sayed, Pieter G. Postema, Mareen Datema, Laura van Dussen, Jan A. Kors, Cato C. ter Haar, Hidde Bleijendaal, Henrike Galenkamp, Bert-Jan H. van den Born, Carla E. M. Hollak, Mirjam Langeveld

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

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Neonatal carnitine concentrations in relation to gestational age and weight by Loek L. Crefcoeur, Monique G. M. deSain‐van der Velden, Sacha Ferdinandusse, Mirjam Langeveld, Rose Maase, Frédéric M. Vaz, Gepke Visser, Ronald J.A. Wanders, Frits A. Wijburg, Rendelien K. Verschoof‐Puite, Peter C. J. I. Schielen

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Inherited metabolic disorders in adults: systematic review on patient characteristics and diagnostic yield of broad sequencing techniques (exome and genome sequencing) by Elise A. Ferreira, Elise A. Ferreira, Mark J. N. Buijs, Mark J. N. Buijs, Robin Wijngaard, Robin Wijngaard, Joost G. Daams, Mareen R. Datema, Marc Engelen, Clara D. M. van Karnebeek, Clara D. M. van Karnebeek, Clara D. M. van Karnebeek, Machteld M. Oud, Machteld M. Oud, Frédéric M. Vaz, Frédéric M. Vaz, Mirjam M. C. Wamelink, Saskia N. van der Crabben, Mirjam Langeveld

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