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.

Impact of NBS for VLCAD 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, Rubio Gozalbo Estela, van der Velden Monique G M de Sain-, 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.

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

Identification of a Loss-of-Function Mutation in the Context of Glutaminase Deficiency and Neonatal Epileptic Encephalopathy

Rumping Lynne, Büttner Benjamin, Maier Oliver, Rehmann Holger, Lequin Maarten, Schlump Jan-Ulrich, Schmitt Bernhard, Schiebergen-Bronkhorst Birgit, Prinsen Hubertus C M T, Losa Michele, Fingerhut Ralph, Lemke Johannes R, Zwartkruis Fried J T, Houwen Roderick H J, Jans Judith J M, Verhoeven-Duif Nanda M, van Hasselt Peter M, Jamra Rami 21 Dec 2018 In: JAMA Neurology.

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.

Aminoacyl-tRNA synthetase deficiencies: in search of common themes

Kok G, Schene IF, Nikkels PGJ, van Gassen KLI, Terheggen-Lagro Suzanne W.J., van der Crabben SN, Niers L.E.M., Wolf V.I., de Vries M.C., Koolen D.A., Houwen RHJ, Mulder M.F., van Hasselt PM, Fuchs SA 4 Sep 2018 p. 1 1 p.

Aminoacyl-tRNA synthetase deficiencies: in search of common themes

Kok G, Schene IF, Nikkels PGJ, van Gassen KLI, Terheggen-Lagro Suzanne W.J., van der Crabben SN, Hoeks Sanne B. E. A., Niers Laetitia E.M., Wolf Nicole I., de Vries Maaike C., Koolen David A., Houwen RHJ, Mulder Margot F., van Hasselt PM, Fuchs SA 4 Sep 2018 2 p.

Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome?

de Rooy R. L.P., Halbertsma F. J., Struijs E. A., van Spronsen F. J., Lunsing R. J., Schippers H. M., van Hasselt P. M., Plecko B., Wohlrab G., Whalen S., Benoist J. F., Valence S., Mills P. B., Bok L. A. 1 Jul 2018 In: European Journal of Paediatric Neurology. 22, p. 662-666 5 p.

All Research Output (99)

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Research programs

Biography

Research Output

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