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.

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, 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.

Autism spectrum disorder: an early and frequent feature in cerebrotendinous xanthomatosis

Stelten Bianca M L, Bonnot Olivier, Huidekoper Hidde H., van Spronsen Francjan J., van Hasselt Peter M, Kluijtmans Leo A J, Wevers Ron A., Verrips Aad Jul 2018 In: Journal of Inherited Metabolic Disease. 41, p. 641-646

Early and late outcomes after cord blood transplantation for pediatric patients with inherited leukodystrophies

van den Broek Brigitte T A, Page Kristin M., Paviglianiti Annalisa, Hol Janna, Allewelt Heather, Volt Fernanda, Michel Gerard, Diaz Miguel Angel, Bordon Victoria, O'Brien Tracey A., Shaw Peter J., Kenzey Chantal, Al-Seraihy Amal, van Hasselt Peter M, Gennery Andrew R., Gluckman Eliane, Rocha Vanderson, Ruggeri Annalisa, Kurtzberg Joanne, Boelens Jaap Jan 9 Jan 2018 In: Blood. 2, p. 49-60 12 p.

Incomplete biomarker response in mucopolysaccharidosis type I after successful hematopoietic cell transplantation

Kuiper Gé Ann, van Hasselt Peter M., Boelens Jaap Jan, Wijburg Frits A., Langereis Eveline J. Sep 2017 In: Molecular Genetics and Metabolism. 122, p. 86–91

Hypothesis: Lobe A (COG1-4)-CDG causes a more severe phenotype than lobe B (COG5-8)-CDG

Haijes Hanneke A, Jaeken Jaak, Foulquier François, van Hasselt Peter M 28 Aug 2017 In: Journal of Medical Genetics. 55, p. 137-142 6 p.

Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy

Ait-El-Mkadem Samira, Dayem-Quere Manal, Gusic Mirjana, Chaussenot Annabelle, Bannwarth Sylvie, François Bérengère, Genin Emmanuelle C, Fragaki Konstantina, Volker-Touw Catharina L M, Vasnier Christelle, Serre Valérie, van Gassen Koen L I, Lespinasse Françoise, Richter Susan, Eisenhofer Graeme, Rouzier Cécile, Mochel Fanny, De Saint-Martin Anne, Abi Warde Marie-Thérèse, de Sain-van der Velden Monique G M, Jans Judith J M, Amiel Jeanne, Avsec Ziga, Mertes Christian, Haack Tobias B, Strom Tim, Meitinger Thomas, Bonnen Penelope E, Taylor Robert W, Gagneur Julien, van Hasselt Peter M, Rötig Agnès, Delahodde Agnès, Prokisch Holger, Fuchs Sabine A, Paquis-Flucklinger Véronique 10 Dec 2016 In: American Journal of Human Genetics. 100, p. 151–159

Is FGF13 a major contributor to genetic epilepsy with febrile seizures plus?

Rigbye Kristin A., van Hasselt Peter M., Burgess Rosemary, Damiano John A., Mullen Saul A., Petrovski Slavé, Puranam Ram S., van Gassen Koen L I, Gecz Jozef, Scheffer Ingrid E., McNamara James O., Berkovic Samuel F., Hildebrand Michael S. 1 Dec 2016 In: Epilepsy Research. 128, p. 48-51 4 p.

All Research Output (72)

Contact

Research programs

Biography

Research Output

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