van Hasselt PM - Search Results

1

Metabolic fingerprinting reveals extensive consequences of GLS hyperactivity.

Rumping L, Pras-Raves ML, Gerrits J, Tang YF, Willemsen MA, Houwen RHJ, van Haaften G, van Hasselt PM, Verhoeven-Duif NM, Jans JJM. Rumping L, et al. Among authors: van hasselt pm, van haaften g. Biochim Biophys Acta Gen Subj. 2020 Mar;1864(3):129484. doi: 10.1016/j.bbagen.2019.129484. Epub 2019 Nov 14. Biochim Biophys Acta Gen Subj. 2020. PMID: 31734463 Free article.

2

[Vitamin K deficiency bleeding in an infant despite adequate prophylaxis].

van Hasselt PM, Houwen RH, van Dijk AT, de Koning TJ. van Hasselt PM, et al. Among authors: van dijk at. Ned Tijdschr Geneeskd. 2003 Apr 19;147(16):737-40. Ned Tijdschr Geneeskd. 2003. PMID: 12731461 Dutch.

3

Prevention of vitamin K deficiency bleeding in breastfed infants: lessons from the Dutch and Danish biliary atresia registries.

van Hasselt PM, de Koning TJ, Kvist N, de Vries E, Lundin CR, Berger R, Kimpen JL, Houwen RH, Jorgensen MH, Verkade HJ; Netherlands Study Group for Biliary Atresia Registry. van Hasselt PM, et al. Pediatrics. 2008 Apr;121(4):e857-63. doi: 10.1542/peds.2007-1788. Pediatrics. 2008. PMID: 18381514

4

Vitamin K deficiency bleeding in cholestatic infants with alpha-1-antitrypsin deficiency.

van Hasselt PM, Kok K, Vorselaars AD, van Vlerken L, Nieuwenhuys E, de Koning TJ, de Vries RA, Houwen RH. van Hasselt PM, et al. Among authors: van vlerken l. Arch Dis Child Fetal Neonatal Ed. 2009 Nov;94(6):F456-60. doi: 10.1136/adc.2008.148239. Epub 2009 May 3. Arch Dis Child Fetal Neonatal Ed. 2009. PMID: 19414430

5

Hydrolysed formula is a risk factor for vitamin K deficiency in infants with unrecognised cholestasis.

van Hasselt PM, de Vries W, de Vries E, Kok K, Cranenburg EC, de Koning TJ, Schurgers LJ, Verkade HJ, Houwen RH. van Hasselt PM, et al. J Pediatr Gastroenterol Nutr. 2010 Dec;51(6):773-6. doi: 10.1097/MPG.0b013e3181efb0b3. J Pediatr Gastroenterol Nutr. 2010. PMID: 21057325

6

Application of exome sequencing in the search for genetic causes of rare disorders of copper metabolism.

Fuchs SA, Harakalova M, van Haaften G, van Hasselt PM, Cuppen E, Houwen RH. Fuchs SA, et al. Among authors: van hasselt pm, van haaften g. Metallomics. 2012 Jul;4(7):606-13. doi: 10.1039/c2mt20034a. Epub 2012 May 4. Metallomics. 2012. PMID: 22555275 Review.

7

The Proline/Citrulline Ratio as a Biomarker for OAT Deficiency in Early Infancy.

de Sain-van der Velden MG, Rinaldo P, Elvers B, Henderson M, Walter JH, Prinsen BH, Verhoeven-Duif NM, de Koning TJ, van Hasselt P. de Sain-van der Velden MG, et al. JIMD Rep. 2012;6:95-9. doi: 10.1007/8904_2011_122. Epub 2012 Feb 24. JIMD Rep. 2012. PMID: 23430945 Free PMC article.

8

Supplementation with a powdered blend of PUFAs normalizes DHA and AA levels in patients with PKU.

Jans JJ, de Sain-van der Velden MG, van Hasselt PM, van den Hurk DT, Vaz FM, Visser G, Verhoeven-Duif NM. Jans JJ, et al. Among authors: van hasselt pm, van den hurk dt. Mol Genet Metab. 2013 Jun;109(2):121-4. doi: 10.1016/j.ymgme.2013.03.006. Epub 2013 Mar 21. Mol Genet Metab. 2013. PMID: 23562298

9

Impaired cognitive functioning in patients with tyrosinemia type I receiving nitisinone.

Bendadi F, de Koning TJ, Visser G, Prinsen HC, de Sain MG, Verhoeven-Duif N, Sinnema G, van Spronsen FJ, van Hasselt PM. Bendadi F, et al. Among authors: van hasselt pm, van spronsen fj. J Pediatr. 2014 Feb;164(2):398-401. doi: 10.1016/j.jpeds.2013.10.001. Epub 2013 Nov 14. J Pediatr. 2014. PMID: 24238861 Free article.

10

Survival and psychomotor development with early betaine treatment in patients with severe methylenetetrahydrofolate reductase deficiency.

Diekman EF, de Koning TJ, Verhoeven-Duif NM, Rovers MM, van Hasselt PM. Diekman EF, et al. Among authors: van hasselt pm. JAMA Neurol. 2014 Feb;71(2):188-94. doi: 10.1001/jamaneurol.2013.4915. JAMA Neurol. 2014. PMID: 24323041 Review.

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