F J Van Spronsen - JoVE Visualize

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Molecular Genetics and Metabolism|August 7, 2009

MR spectroscopy and diffusion tensor imaging of the brain in Sjögren-Larsson syndromeP E Sijens, H E Westerlaan, J C de Groot, et al.

Acta Paediatrica (Oslo, Norway : 1992)|August 1, 1997

Does impaired growth of PKU patients correlate with the strictness of dietary treatment? National Dutch PKU Steering CommitteeF J van Spronsen, P H Verkerk, M van Houten, et al.

Neuropsychology|September 10, 2003

Motor function under lower and higher controlled processing demands in early and continuously treated phenylketonuriaS C J Huijbregts, L M J De Sonneville, F J Van Spronsen, et al.

Molecular Genetics and Metabolism|March 26, 2021

Effect of BH4 on blood phenylalanine and tyrosine variations in patients with phenylketonuriaAmj van Wegberg, Raf Evers, Jgm Burgerhof, et al.

Molecular Genetics and Metabolism|June 12, 2026

Toward personalized treatment in phenylketonuria: Intra-individual variation of in vivo phenylalanine oxidation using the 13C-phenylalanine breath testS Haitjema, E M van Steenis, R A F Evers, et al.

Molecular Genetics and Metabolism|November 30, 2006

Partial hypoxanthine-guanine phosphoribosyl transferase deficiency without elevated urinary hypoxanthine excretionC M L van Dael, L J W M Pierik, D J Reijngoud, et al.

Journal of Inherited Metabolic Disease|January 26, 2006

Normal very-long-chain fatty acids in peroxisomal D-bifunctional protein deficiency: a diagnostic pitfallR J Soorani-Lunsing, F J van Spronsen, I Stolte-Dijkstra, et al.

Molecular Genetics and Metabolism|September 30, 2006

Tyrosinemia type I treated by NTBC: how does AFP predict liver cancer?C J L Koelink, P van Hasselt, A van der Ploeg, et al.

Molecular Genetics and Metabolism|March 28, 2025

Inter-individuality in the transport and effect of phenylalanine in the brain: A double case report of two 'unusual' phenylketonuria patientsE M van Steenis, S C J Huijbregts, D Draaisma-van Vliet, et al.

Journal of Inherited Metabolic Disease|October 14, 2000

Behaviour and school achievement in patients with early and continuously treated phenylketonuriaB A Stemerdink, A F Kalverboer, J J van der Meere, et al.

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Showing results (41-50 of 72) with videos related to

Sort By:

Pageof 8

Molecular Genetics and Metabolism|August 7, 2009

MR spectroscopy and diffusion tensor imaging of the brain in Sjögren-Larsson syndromeP E Sijens, H E Westerlaan, J C de Groot, et al.

Acta Paediatrica (Oslo, Norway : 1992)|August 1, 1997

Does impaired growth of PKU patients correlate with the strictness of dietary treatment? National Dutch PKU Steering CommitteeF J van Spronsen, P H Verkerk, M van Houten, et al.

Neuropsychology|September 10, 2003

Motor function under lower and higher controlled processing demands in early and continuously treated phenylketonuriaS C J Huijbregts, L M J De Sonneville, F J Van Spronsen, et al.

Molecular Genetics and Metabolism|March 26, 2021

Effect of BH4 on blood phenylalanine and tyrosine variations in patients with phenylketonuriaAmj van Wegberg, Raf Evers, Jgm Burgerhof, et al.

Molecular Genetics and Metabolism|June 12, 2026

Toward personalized treatment in phenylketonuria: Intra-individual variation of in vivo phenylalanine oxidation using the 13C-phenylalanine breath testS Haitjema, E M van Steenis, R A F Evers, et al.

Molecular Genetics and Metabolism|November 30, 2006

Partial hypoxanthine-guanine phosphoribosyl transferase deficiency without elevated urinary hypoxanthine excretionC M L van Dael, L J W M Pierik, D J Reijngoud, et al.

Journal of Inherited Metabolic Disease|January 26, 2006

Normal very-long-chain fatty acids in peroxisomal D-bifunctional protein deficiency: a diagnostic pitfallR J Soorani-Lunsing, F J van Spronsen, I Stolte-Dijkstra, et al.

Molecular Genetics and Metabolism|September 30, 2006

Tyrosinemia type I treated by NTBC: how does AFP predict liver cancer?C J L Koelink, P van Hasselt, A van der Ploeg, et al.

Molecular Genetics and Metabolism|March 28, 2025

Inter-individuality in the transport and effect of phenylalanine in the brain: A double case report of two 'unusual' phenylketonuria patientsE M van Steenis, S C J Huijbregts, D Draaisma-van Vliet, et al.

Journal of Inherited Metabolic Disease|October 14, 2000

Behaviour and school achievement in patients with early and continuously treated phenylketonuriaB A Stemerdink, A F Kalverboer, J J van der Meere, et al.

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