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Associate Professor C. van Fluit

Associate Professor C. van Fluit

Associate Professor - medical
Associate Professor C. van Fluit
  • Metabolic diseases patient care

Biography

Biography

2020-present       Research Manager WKZ

2019-present       Associate Professor (Universitair hoofddocent UHD)

2017-present       Head of subspecialty Metabolic diseases (from August 2018)

2017-2020          Head of Cluster C (subspecialties Endocrinology, Metabolic diseases, MDL, Nephrology) at WKZ  

2015-present       'Opleider' at department of Metabolic Diseases     

2009-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)

Side Activities

  • Member of Horizon scan chamber (ZIN (Zorg Instituut Nederland, previously VWS) ‘Metabolic & Endocrine disorders’, (from 2016 onwards), (no payments)
  • Member of the board of the WKZ research fund, (from 2020 onwards), (no payments)
  • Advisor for the Dutch Health Council (Gezondheidsraad) committee in a recent adaptation, (2017), (no payments)
  • Advisor for the Dutch Health Council (Gezondheidsraad) committee ‘nutrition’ with regards vitamin K, (2010), (no payments)
  • Speaker Orchid meeting, (2022), (<€2200.-)

Research Output (162)

Modified Delphi procedure-based expert consensus on endpoints for an international disease registry for Metachromatic Leukodystrophy:The European Metachromatic Leukodystrophy initiative (MLDi)

Schoenmakers Daphne H., Beerepoot Shanice, van den Berg Sibren, Adang Laura, Bley Annette, Boelens Jaap Jan, Fumagalli Francesca, Goettsch Wim G., Grønborg Sabine, Groeschel Samuel, van Hasselt Peter M., Hollak Carla E.M., Lindemans Caroline, Mochel Fanny, Mol Peter G.M., Sevin Caroline, Zerem Ayelet, Schöls Ludger, Wolf Nicole I. 14 Feb 2022, In: Orphanet Journal of Rare Diseases. 17

Internalization and transport of PEGylated lipid-based mixed micelles across Caco-2 cells mediated by scavenger receptor B1

Su Xiangjie, Ramírez-Escudero Mercedes, Sun Feilong, van den Dikkenberg Joep B., van Steenbergen Mies J., Pieters Roland J., Janssen Bert J.C., van Hasselt Peter M., Hennink Wim E., van Nostrum Cornelus F. Dec 2021, In: Pharmaceutics. 13

Therapy-type related long-term outcomes in mucopolysaccaridosis type II (Hunter syndrome) – Case series

Zerjav Tansek Mojca, Kodric Jana, Klemencic Simona, Boelens Jaap Jan, van Hasselt Peter M., Drole Torkar Ana, Doric Maja, Koren Alenka, Avcin Simona, Battelino Tadej, Groselj Urh Sep 2021, In: Molecular Genetics and Metabolism Reports. 28

Novel Orally Formulated Mixed Micelles Optimize Vitamin K Absorption Under Bile-Deficient Conditions

Rooimans Thijs, Minderhoud Tanca, Leal Nerea, Vromans Herman, van Nostrum Cornelus, van Hasselt Peter, Rodriguez M., Sun F., Oussoren C., Slot T. K., van der Ham M., Janssens G. E.P.J., de Sain-van der Velden M. G.M., Houwen R. H.J., de Koning T. J., Hennink W. E., Sep 2021, In: Gastroenterology. 161 , p. 1056-1059.e5

Long-term effect of hematopoietic cell transplantation on systemic inflammation in patients with mucopolysaccharidoses

van den Broek Brigitte T A, Lindemans Caroline A, Boelens Jaap Jan, Delemarre Eveline M, Drylewicz Julia, Verhoeven-Duif Nanda, van Hasselt Peter M, Nierkens Stefan 24 Aug 2021, In: Blood Advances. 5 , p. 3092-3101 10 p.

Beyond nephronophthisis:Retinal dystrophy in the absence of kidney dysfunction in childhood expands the clinical spectrum of CEP83 deficiency

Veldman Bram C.F., Kuper Willemijn F.E., Lilien Marc, Schuurs-Hoeijmakers Janneke H.M., Marcelis Carlo, Phan Milan, Hettinga Ymkje, Talsma Herman E., van Hasselt Peter M., Haijes Hanneke A. Jul 2021, In: American Journal of Medical Genetics, Part A. 185 , p. 2204-2210 7 p.

Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

Parenti Ilaria, Lehalle Daphné, Nava Caroline, Torti Erin, Leitão Elsa, Person Richard, Mizuguchi Takeshi, Matsumoto Naomichi, Kato Mitsuhiro, Nakamura Kazuyuki, de Man Stella A., Cope Heidi, Shashi Vandana, Friedman Jennifer, Joset Pascal, Steindl Katharina, Rauch Anita, Muffels Irena, van Hasselt Peter M., Petit Florence, Smol Thomas, Le Guyader Gwenaël, Bilan Frédéric, Sorlin Arthur, Vitobello Antonio, Philippe Christophe, van de Laar Ingrid M.B.H., van Slegtenhorst Marjon A., Campeau Philippe M., Au Ping Yee Billie, Nakashima Mitsuko, Saitsu Hirotomo, Yamamoto Tatsuya, Nomura Yumiko, Louie Raymond J., Lyons Michael J., Dobson Amy, Plomp Astrid S., Motazacker M. Mahdi, Kaiser Frank J., Timberlake Andrew T., Fuchs Sabine A., Depienne Christel, Mignot Cyril, Acosta Maria T., Adam Margaret, Adams David R., Agrawal Pankaj B., Alejandro Mercedes E., Alvey Justin, 4 May 2021, In: Human Genetics. 140 , p. 1109-1120 12 p.

Automatic quantification of lymphocyte vacuolization in peripheral blood smears of patients with Batten's disease (CLN3 disease)

Nonkes Lourens J P, Kuper Willemijn F E, Berrens-Hogenbirk Karin, Musson Ruben E A, van Hasselt Peter M, Huisman Albert 1 Mar 2021, In: JIMD Reports. 58 , p. 100-103 4 p.

Quantifying the Effects of Hip Surgery on the Sphericity of the Femoral Head in Patients with Mucopolysaccharidosis Type I

van der Veer Eline L., Gielis Willem Paul, Weinans Harry, Beek Erik J., van Hasselt Peter M., Sakkers Ralph J.B. 12 Jan 2021, In: The Journal of bone and joint surgery. American volume. 103 , p. 489-496 8 p.

Deep intronic TIMMDC1 variant delays diagnosis of rapidly progressive complex I deficiency

Hellebrekers Debby, Nievelstein Rutger A J, van Hasselt Peter M, van Jaarsveld Richard H, Cuppen Inge, Oegema Renske Jan 2021, In: European Journal of Medical Genetics. 64 5 p.

All research output

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