dr. P.M. van Hasselt Assistant Professor - medical

Cluster C
Metabolic diseases patient care

Contact

phassel2@umcutrecht.nl

Research programs

Child Health

Biography
Research Output

Biography

2018-present Head of subspecialty Metabolic diseases (from August 2018)

2017-present Head of Cluster C (subspecialties Endocrinology, Metabolic diseases, MDL, Nephrology) at WKZ

2015-present 'Opleider' at department of Metabolic Diseases

2010-present Staff member at department of Metabolic Diseases

2007-present Pediatrician for Metabolic Diseases, Wilhelmina Children’s Hospital, Utrecht.

2004-2009: PhD “Vitamin K prophylaxis revisited – focus on risk factors”. Utrecht University. Promotors: Prof.Dr. R. Berger and Prof.dr. J.J.L. Kimpen

2004-2007: Subspecialty training (fellowship) for Metabolic Diseases, Wilhelmina Children’s Hospital. Head: Dr. T.J. de Koning

1999-2004: Pediatric specialty training. Wilhelmina Children’s Hospital, Utrecht and Isala Clinics, Zwolle. Head: Prof.dr. J.J.L. Kimpen

1998-1999: Physician-researcher at Netherlands Institute of Neuroscience, Amsterdam. Head: Prof R. Buis;

1997-1998: Physician at Department of Neonatology, Wilhelmina Children’s Hospital, Utrecht

1994-1997: Artsexamen (MD), University of Groningen

1989-1994: Doctoral Medicine (MSc), University of Groningen

1988-1989: Freshman-year at Wittenburg University, Springfield OH, USA (supported by scholarship through NACEE, now known as Fulbright Center)

Research Output

Impact of newborn screening for very-long-chain acyl-CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes(Article)(Open Access)

Bleeker Jeannette, Kok I., Ferdinandusse S., van der Pol WL, Cuppen Inge, Bosch A.M., Langeveld Mirjam, Derks Terry G J, Williams Monique, de Vries M., Mulder M.F., Gozalbo Estela Rubio, de Sain-van der Velden Monique, Rennings Alexander J M, Schielen Peter, Dekkers Eugenie, Houtkooper Riekelt H., Waterman H, Pras-Raves Mia, Wanders RJH, van Hasselt PM, Schoenmakers Marja, Wijburg FA, Visser Gepke 1 May 2019 In: Journal of Inherited Metabolic Disease. 42, p. 414 423 p.

Direct-infusion based metabolomics unveils biochemical profiles of inborn errors of metabolism in cerebrospinal fluid

Haijes Hanneke A, van der Ham Maria, Gerrits Johan, van Hasselt Peter M, Prinsen Hubertus C M T, de Sain-van der Velden Monique G M, Verhoeven-Duif Nanda M, Jans Judith J M May 2019 In: Molecular Genetics and Metabolism. 127, p. 51-57 7 p.

Impact of newborn screening for very-long-chain acyl-CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes

Bleeker Jeannette C., Kok Irene L., Ferdinandusse Sacha, van der Pol W. Ludo, Cuppen Inge, Bosch Annet M., Langeveld Mirjam, Derks Terry G.J., Williams Monique, de Vries Maaike, Mulder Margot F., Gozalbo Estela R., de Sain-van der Velden Monique G.M., Rennings Alexander J., Schielen Peter J.C.I., Dekkers Eugenie, Houtkooper Riekelt H., Waterham Hans R., Pras-Raves Mia L., Wanders Ronald J.A., van Hasselt Peter M., Schoenmakers Marja, Wijburg Frits A., Visser Gepke 13 Feb 2019 In: Journal of Inherited Metabolic Disease. 42, p. 414-423 10 p.

Treatment of thoracolumbar kyphosis in patients with mucopolysaccharidosis type I: Results of an international consensus procedure

Kuiper Gé Ann, Langereis Eveline J., Breyer Sandra, Carbone Marco, Castelein René M., Eastwood Deborah M., Garin Christophe, Guffon Nathalie, Van Hasselt Peter M., Hensman Pauline, Jones Simon A., Kenis Vladimir, Kruyt Moyo, Van Der Lee Johanna H., Mackenzie William G., Orchard Paul J., Oxborrow Neil, Parini Rossella, Robinson Amy, Schubert Hjalmarsson Elke, White Klane K., Wijburg Frits A. 18 Jan 2019 In: Orphanet Journal of Rare Diseases. 14

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay

Machol Keren, Rousseau Justine, Ehresmann Sophie, Garcia Thomas, Nguyen Thi Tuyet Mai, Spillmann Rebecca C., Sullivan Jennifer A., Shashi Vandana, Jiang Yong hui, Stong Nicholas, Fiala Elise, Willing Marcia, Pfundt Rolph, Kleefstra Tjitske, Cho Megan T., McLaughlin Heather, Rosello Piera Monica, Orellana Carmen, Martínez Francisco, Caro-Llopis Alfonso, Monfort Sandra, Roscioli Tony, Nixon Cheng Yee, Buckley Michael F., Turner Anne, Jones Wendy D., van Hasselt Peter M., Hofstede Floris C., van Gassen Koen L.I., Brooks Alice S., van Slegtenhorst Marjon A., Lachlan Katherine, Sebastian Jessica, Madan-Khetarpal Suneeta, Sonal Desai, Sakkubai Naidu, Thevenon Julien, Faivre Laurence, Maurel Alice, Petrovski Slavé, Krantz Ian D., Tarpinian Jennifer M., Rosenfeld Jill A., Lee Brendan H., Adams David R., Alejandro Mercedes E., Allard Patrick, Azamian Mahshid S., Bacino Carlos A., Balasubramanyam Ashok, 3 Jan 2019 In: American Journal of Human Genetics. 104, p. 164-178 15 p.

Direct infusion based metabolomics identifies metabolic disease in patients’ dried blood spots and plasma

Haijes Hanneke A., Willemsen Marcel, van der Ham Maria, Gerrits Johan, Pras-Raves Mia L., Prinsen Hubertus C.M.T., van Hasselt Peter M., de Sain-Van der Velden Monique G.M., Verhoeven-Duif Nanda M., Jans Judith J.M. 1 Jan 2019 In: Metabolites. 9

GLS hyperactivity causes glutamate excess, infantile cataract and profound developmental delay

Rumping Lynne, Tessadori Federico, Pouwels Petra J.W., Vringer Esmee, Wijnen Jannie P., Bhogal Alex A., Savelberg Sanne M.C., Duran Karen J., Bakkers Mark J.G., Ramos Rúben J.J., Schellekens Peter A.W., Kroes Hester Y., Klomp Dennis W.J., Black Graeme C.M., Taylor Rachel L., Bakkers Jeroen P.W., Prinsen Hubertus C.M.T., van der Knaap Marjo S., Dansen Tobias B., Rehmann Holger, Zwartkruis Fried J.T., Houwen Roderick H.J., van Haaften Gijs, Verhoeven-Duif Nanda M., Jans Judith J.M., van Hasselt Peter M. 1 Jan 2019 In: Human Molecular Genetics. 28, p. 96-104 9 p.

Bi-allelic mutations in TRAPPC2L result in a neurodevelopmental disorder and have an impact on RAB11 in fibroblasts

Milev Miroslav P., Graziano Claudio, Karall Daniela, Kuper Willemijn F.E., Al-Deri Noraldin, Cordelli Duccio Maria, Haack Tobias B., Danhauser Katharina, Iuso Arcangela, Palombo Flavia, Pippucci Tommaso, Prokisch Holger, Saint-Dic Djenann, Seri Marco, Stanga Daniela, Cenacchi Giovanna, Van Gassen Koen L.I., Zschocke Johannes, Fauth Christine, Mayr Johannes A., Sacher Michael, Van Hasselt Peter M. Nov 2018 In: Journal of Medical Genetics. 55, p. 753-764

Mixed micellar system stabilized with saponins for oral delivery of vitamin K

Sun Feilong, Ye Chengpei, Thanki Kaushik, Leng Donglei, van Hasselt Peter M., Hennink Wim E., van Nostrum Cornelus F. 1 Oct 2018 In: Colloids and Surfaces B: Biointerfaces. 170, p. 521-528 8 p.

Influence of PEGylation of Vitamin-K-Loaded Mixed Micelles on the Uptake by and Transport through Caco-2 Cells

Sun Feilong, Adrian Max, Beztsinna Nataliia, van den Dikkenberg Joep B, Maas-Bakker Roel F, van Hasselt Peter M, van Steenbergen Mies J, Su Xiangjie, Kapitein Lukas C, Hennink Wim E, van Nostrum Cornelus F 4 Sep 2018 In: Molecular pharmaceutics. 15, p. 3786-3795 10 p.

All Research Output (112)

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Research programs

Biography

Research Output

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