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dr. H.C.M.T. Prinsen

dr. H.C.M.T. Prinsen

Assistant Professor

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Research Output (73)

Differences between acylcarnitine profiles in plasma and bloodspots

de Sain - van der Velden M.G.M., Diekman E.F., Jans J.J.M., van der Ham M., Prinsen B.H., Visser G., Verhoeven N.M. 2013, In: Molecular Genetics and Metabolism. 110 , p. 116-21 6 p.

The proline/citrulline ratio as a biomarker for OAT deficiency in early infancy

de Sain - van der Velden M.G.M., Rinaldo P., Elvers B., Henderson M., Walter J.H., Prinsen H.C.M.T., Verhoeven - Duif N.M., de Koning T.J., van Hasselt P.M. 1 Jan 2012, In: JIMD Reports. 6 , p. 95-99 5 p.

Uitbreiding neonatale screeningsprogramma met propionacidemie en methylmalonacidemie is zinvol.

de Sain - van der Velden M.G.M., Bosch A.M., Prinsen H.C.M.T., van Hasselt P.M., Hofstede F.C., Wijburg F.A., Visser G. 2011, In: Nederlands Tijdschrift voor Klinische Chemie en Laboratoriumgeneeskunde. 36 , p. 167-169 3 p.

Clinical exercise testing in children with neurometabolic myopathies

Takken T., Ernsting C., Hulzebos H.J., Groen W.G., van Hasselt P.M., Prinsen H.C.M.T., Helders P.J.M., Visser G. 2011, p. 187-191 4 p.

HIGH INCIDENCE OF HYPERAMMONEMIA IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA RECEIVING PEGYLATED ASPARAGINASE

Heitink-Polle K. M. J., Prinsen B. H. C. M. T., de Koning T. J., Bierings M. B., van Hasselt P. M. 2011, In: Journal of Inherited Metabolic Disease. 34 , p. S89-S89 1 p.

PROLINE/CITRULLINE RATIO AS A BIOMARKER FOR OAT DEFICIENCY IN EARLY INFANCY

de Sain-van der Velden M. G. M., Rinaldo P., Elvers B., Prinsen H. C. M. T., Verhoeven-Duif N. M., de Koning T. J., van Hasselt P. 2011, In: Journal of Inherited Metabolic Disease. 34 , p. S252-S252 1 p.

A 2D-DIGE approach to identify proteins involved in inside-out control of integrins (Journal Proteome Research (2009) 8, (3824-3833))

Langereis Jeroen D., Prinsen Berthil H.C.M.T., De Sain-van Der Velden Monique G.M., Coppens Cornelis J.C., Koenderman Leo, Ulfman Laurien H. 4 Jan 2010, In: Journal of Proteome Research. 9 1 p.

GAMT-deficiëntie: een behandelbare stoornis in de creatinestofwisseling

Dam B.J.G., Prinsen H.C.M.T., Hofstede F.C., Salomons G.S., Visser G. 2010, In: Tijdschrift voor Kindergeneeskunde. 78 , p. 209-212 4 p.

Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.

Lubbehusen J., Thiel C., Rind N., Ungar D., Prinsen H.C.M.T., de Koning T.J., van Hasselt P.M., Korner C. 2010, In: Human Molecular Genetics. 19 , p. 3623-3633 11 p.

Dried blood spot analysis:an easy and reliable tool to monitor the biochemical effect of hematopoietic stem cell transplantation in hurler syndrome patients

Aldenhoven M., de Koning T.J., Verheijen F.W., Prinsen H.C.M.T., Wijburg F.A., van der Ploeg AT, de Sain - van der Velden M.G.M., Boelens J.J. 2010, In: Biology of Blood and Marrow Transplantation. 16 , p. 701-704 4 p.

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