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	1.	Neurodevelopmental Outcome after Hematopoietic Cell Transplantation in Inborn Errors of Metabolism: Current Considerations and Future Perspectives. [electronic resource] by Boelens, Jaap Jan van Hasselt, Peter M Producer: 20170221 In: Neuropediatrics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS. [electronic resource] by Rumping, Lynne Jans, Judith J van Hasselt, Peter M Producer: 20190920 In: The New England journal of medicine vol. 381 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Monocarboxylate transporter 1 deficiency and ketone utilization. [electronic resource] by van Hasselt, Peter M Ferdinandusse, Sacha van Haaften, Gijs Producer: 20150219 In: The New England journal of medicine vol. 372 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Hypothesis: determining phenotypic specificity facilitates understanding of pathophysiology in rare genetic disorders. [electronic resource] by Haijes, Hanneke A Jaeken, Jaak van Hasselt, Peter M Producer: 20210823 In: Journal of inherited metabolic disease vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Hypothesis: lobe A (COG1-4)-CDG causes a more severe phenotype than lobe B (COG5-8)-CDG. [electronic resource] by Haijes, Hanneke A Jaeken, Jaak Foulquier, François van Hasselt, Peter M Producer: 20190910 In: Journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Glucose transporter type 1 deficiency syndrome and the ketogenic diet. [electronic resource] by Schwantje, Marit Verhagen, Lilly M van Hasselt, Peter M Fuchs, Sabine A Producer: 20210702 In: Journal of inherited metabolic disease vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	[Hereditary fructose intolerance]. [electronic resource] by Rumping, Lynne Waterham, Hans R Kok, Irene van Hasselt, Peter M Visser, Gepke Producer: 20141121 In: Nederlands tijdschrift voor geneeskunde vol. 158 Availability: No items available. Save to lists Add to cart (remove)
	8.	Pathophysiology of propionic and methylmalonic acidemias. Part 2: Treatment strategies. [electronic resource] by Haijes, Hanneke A van Hasselt, Peter M Jans, Judith J M Verhoeven-Duif, Nanda M Producer: 20200916 In: Journal of inherited metabolic disease vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Incomplete biomarker response in mucopolysaccharidosis type I after successful hematopoietic cell transplantation. [electronic resource] by Kuiper, Gé-Ann van Hasselt, Peter M Boelens, Jaap Jan Wijburg, Frits A Langereis, Eveline J Producer: 20180518 In: Molecular genetics and metabolism vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A Mixed Micelle Formulation for Oral Delivery of Vitamin K. [electronic resource] by Sun, Feilong Jaspers, Tessa C C van Hasselt, Peter M Hennink, Wim E van Nostrum, Cornelus F Producer: 20171204 In: Pharmaceutical research vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Intracranial bleeding due to vitamin K deficiency: advantages of using a pediatric intensive care registry. [electronic resource] by Visser, Désirée Y Jansen, Nicolaas J Ijland, Marloes M de Koning, Tom J van Hasselt, Peter M Producer: 20110930 In: Intensive care medicine vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Application of exome sequencing in the search for genetic causes of rare disorders of copper metabolism. [electronic resource] by Fuchs, Sabine A Harakalova, Magdalena van Haaften, Gijs van Hasselt, Peter M Cuppen, Edwin Houwen, Roderick H J Producer: 20121029 In: Metallomics : integrated biometal science vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Pathophysiology of propionic and methylmalonic acidemias. Part 1: Complications. [electronic resource] by Haijes, Hanneke A Jans, Judith J M Tas, Simone Y Verhoeven-Duif, Nanda M van Hasselt, Peter M Producer: 20200916 In: Journal of inherited metabolic disease vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Survival and psychomotor development with early betaine treatment in patients with severe methylenetetrahydrofolate reductase deficiency. [electronic resource] by Diekman, Eugene F de Koning, Tom J Verhoeven-Duif, Nanda M Rovers, Maroeska M van Hasselt, Peter M Producer: 20140408 In: JAMA neurology vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Mixed micellar system stabilized with saponins for oral delivery of vitamin K. [electronic resource] by Sun, Feilong Ye, Chengpei Thanki, Kaushik Leng, Donglei van Hasselt, Peter M Hennink, Wim E van Nostrum, Cornelus F Producer: 20181105 In: Colloids and surfaces. B, Biointerfaces vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Expanding the clinical phenotype of COG6 deficiency. [electronic resource] by Haijes, Hanneke Prinsen, Hubertus C M T Thiel, Christian Koerner, Christian Verhoeven-Duif, Nanda M van Hasselt, Peter M Producer: 20150121 In: Journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Inborn errors of enzymes in glutamate metabolism. [electronic resource] by Rumping, Lynne Vringer, Esmee Houwen, Roderick H J van Hasselt, Peter M Jans, Judith J M Verhoeven-Duif, Nanda M Producer: 20210702 In: Journal of inherited metabolic disease vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Timing of cognitive decline in CLN3 disease. [electronic resource] by Kuper, Willemijn F E van Alfen, Claudia Rigterink, Roeliene H Fuchs, Sabine A van Genderen, Maria M van Hasselt, Peter M Producer: 20181226 In: Journal of inherited metabolic disease vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Salivary α-Iduronidase Activity as a Potential New Biomarker for the Diagnosis and Monitoring the Effect of Therapy in Mucopolysaccharidosis Type I. [electronic resource] by van Doorn, Jaap van den Broek, Brigitte T A Geboers, Ans J Kuiper, Gé-Ann Boelens, Jaap J van Hasselt, Peter M Producer: 20190702 In: Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	High incidence of symptomatic hyperammonemia in children with acute lymphoblastic leukemia receiving pegylated asparaginase. [electronic resource] by Heitink-Pollé, Katja M J Prinsen, Berthil H C M T de Koning, Tom J van Hasselt, Peter M Bierings, Marc B Producer: 20130225 In: JIMD reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 87 results.