van Hasselt P - Search Results

1

Yield of additional metabolic studies in neurodevelopmental disorders.

Engbers HM, Berger R, van Hasselt P, de Koning T, de Sain-van der Velden MG, Kroes HY, Visser G. Engbers HM, et al. Among authors: van hasselt p. Ann Neurol. 2008 Aug;64(2):212-7. doi: 10.1002/ana.21435. Ann Neurol. 2008. PMID: 18570304

2

Altered immune function in human newborns after prenatal administration of betamethasone: enhanced natural killer cell activity and decreased T cell proliferation in cord blood.

Kavelaars A, van der Pompe G, Bakker JM, van Hasselt PM, Cats B, Visser GH, Heijnen CJ. Kavelaars A, et al. Among authors: van hasselt pm, van der pompe g. Pediatr Res. 1999 Mar;45(3):306-12. doi: 10.1203/00006450-199903000-00003. Pediatr Res. 1999. PMID: 10088646

3

[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.

4

[From gene to disease; Menkes disease: copper deficiency due to an ATP7A-gene defect].

Aldenhoven M, Klomp LW, van Hasselt PM, de Koning TJ, Visser G. Aldenhoven M, et al. Among authors: van hasselt pm. Ned Tijdschr Geneeskd. 2007 Oct 13;151(41):2266-70. Ned Tijdschr Geneeskd. 2007. PMID: 17987894 Review. Dutch.

5

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

6

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

7

Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.

Lübbehusen J, Thiel C, Rind N, Ungar D, Prinsen BH, de Koning TJ, van Hasselt PM, Körner C. Lübbehusen J, et al. Hum Mol Genet. 2010 Sep 15;19(18):3623-33. doi: 10.1093/hmg/ddq278. Epub 2010 Jul 6. Hum Mol Genet. 2010. PMID: 20605848

8

Exercise stress testing in children with metabolic or neuromuscular disorders.

Takken T, Groen WG, Hulzebos EH, Ernsting CG, van Hasselt PM, Prinsen BH, Helders PJ, Visser G. Takken T, et al. Int J Pediatr. 2010;2010:254829. doi: 10.1155/2010/254829. Epub 2010 Jul 15. Int J Pediatr. 2010. PMID: 20706686 Free PMC article.

9

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

10

Perioperative measures in very long chain acyl-CoA dehydrogenase deficiency.

Vellekoop P, Diekman EF, van Tuijl I, de Vries MM, van Hasselt PM, Visser G. Vellekoop P, et al. Among authors: van hasselt pm, van tuijl i. Mol Genet Metab. 2011 May;103(1):96-7. doi: 10.1016/j.ymgme.2011.01.010. Epub 2011 Jan 27. Mol Genet Metab. 2011. PMID: 21333574

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