Showing results (11-20 of 72) with videos related to
Sort By:
Pageof 8
The American Journal of Clinical Nutrition|February 7, 2001
Phenylketonuria: tyrosine supplementation in phenylalanine-restricted dietsF J van Spronsen, M van Rijn, J Bekhof, et al.Early Human Development|May 1, 2009
Pilot use of the early motor repertoire in infants with inborn errors of metabolism: outcomes in early and middle childhoodJ L M Bruggink, F J van Spronsen, B J Wijnberg-Williams, et al.Nederlands Tijdschrift Voor Geneeskunde|March 8, 2003
[Inherited metabolic diseases and pregnancy: consequences for mother and child]F J van Spronsen, H Molendijk, J J H M Erwich, et al.Molecular Genetics and Metabolism|February 4, 2010
Pathogenesis of cognitive dysfunction in phenylketonuria: review of hypothesesM J de Groot, M Hoeksma, N Blau, et al.Molecular Genetics and Metabolism|December 14, 2005
Cerebral 1H MR spectroscopy showing elevation of brain guanidinoacetate in argininosuccinate lyase deficiencyP E Sijens, D-J Reijngoud, R J Soorani-Lunsing, et al.Molecular Genetics and Metabolism|February 21, 2006
Cerebral 1H MR spectroscopy revealing white matter NAA decreases in glutaric aciduria type IP E Sijens, G P A Smit, L C Meiners, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Predictors of mean phenylalanine levels during the first five years of life in patients with phenylketonuria who were treated early. Dutch National PKU Steering CommitteeP H Verkerk, F J van Spronsen, M van Houten, et al.Journal of Inherited Metabolic Disease|September 10, 2005
Behavioural factors related to metabolic control in patients with phenylketonuriaM R Crone, F J van Spronsen, K Oudshoorn, et al.Neuroscience and Biobehavioral Reviews|December 14, 2002
The neuropsychological profile of early and continuously treated phenylketonuria: orienting, vigilance, and maintenance versus manipulation-functions of working memoryS C J Huijbregts, L M J de Sonneville, F J van Spronsen, et al.Journal of Inherited Metabolic Disease|January 26, 2006
Renal function in tyrosinaemia type I after liver transplantation: a long-term follow-upL J W M Pierik, F J van Spronsen, C M A Bijleveld, et al.Pageof 8