Visser G - Search Results

1

Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies.

Morava E, Tiemes V, Thiel C, Seta N, de Lonlay P, de Klerk H, Mulder M, Rubio-Gozalbo E, Visser G, van Hasselt P, Horovitz DDG, de Souza CFM, Schwartz IVD, Green A, Al-Owain M, Uziel G, Sigaudy S, Chabrol B, van Spronsen FJ, Steinert M, Komini E, Wurm D, Bevot A, Ayadi A, Huijben K, Dercksen M, Witters P, Jaeken J, Matthijs G, Lefeber DJ, Wevers RA. Morava E, et al. Among authors: visser g. J Inherit Metab Dis. 2016 Sep;39(5):759. doi: 10.1007/s10545-016-9967-4. J Inherit Metab Dis. 2016. PMID: 27498540 No abstract available.

2

Tyrosinaemia type I: considerations of treatment strategy and experiences with risk assessment, diet and transplantation.

van Spronsen FJ, Smit GP, Wijburg FA, Thomasse Y, Visser G, Heymans HS. van Spronsen FJ, et al. Among authors: visser g. J Inherit Metab Dis. 1995;18(2):111-4. doi: 10.1007/BF00711742. J Inherit Metab Dis. 1995. PMID: 7564222 No abstract available.

3

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: visser g. Ann Neurol. 2008 Aug;64(2):212-7. doi: 10.1002/ana.21435. Ann Neurol. 2008. PMID: 18570304

4

[Extensive neonatal heel injection screening for metabolic diseases in the Netherlands].

Visser G, van Spronsen FJ, de Sain-van der Velden MG, Blom HJ, Wijburg FA. Visser G, et al. Ned Tijdschr Geneeskd. 2009 May 2;153(18):848-53. Ned Tijdschr Geneeskd. 2009. PMID: 19475862 Dutch. No abstract available.

5

A potential role for muscle in glucose homeostasis: in vivo kinetic studies in glycogen storage disease type 1a and fructose-1,6-bisphosphatase deficiency.

Huidekoper HH, Visser G, Ackermans MT, Sauerwein HP, Wijburg FA. Huidekoper HH, et al. Among authors: visser g. J Inherit Metab Dis. 2010 Feb;33(1):25-31. doi: 10.1007/s10545-009-9030-9. Epub 2010 Feb 2. J Inherit Metab Dis. 2010. PMID: 20127282 Free PMC article.

6

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. Among authors: visser g. Int J Pediatr. 2010;2010:254829. doi: 10.1155/2010/254829. Epub 2010 Jul 15. Int J Pediatr. 2010. PMID: 20706686 Free PMC article.

7

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: visser g. 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

8

Metabolic profiles in children during fasting.

van Veen MR, van Hasselt PM, de Sain-van der Velden MG, Verhoeven N, Hofstede FC, de Koning TJ, Visser G. van Veen MR, et al. Among authors: visser g. Pediatrics. 2011 Apr;127(4):e1021-7. doi: 10.1542/peds.2010-1706. Epub 2011 Mar 21. Pediatrics. 2011. PMID: 21422093

9

Survival, but not maturation, is affected in neutrophil progenitors from GSD-1b patients.

Visser G, de Jager W, Verhagen LP, Smit GP, Wijburg FA, Prakken BJ, Coffer PJ, Buitenhuis M. Visser G, et al. J Inherit Metab Dis. 2012 Mar;35(2):287-300. doi: 10.1007/s10545-011-9379-4. Epub 2011 Aug 24. J Inherit Metab Dis. 2012. PMID: 21863279

10

Acid sphingomyelinase (Asm) deficiency patients in The Netherlands and Belgium: disease spectrum and natural course in attenuated patients.

Hollak CE, de Sonnaville ES, Cassiman D, Linthorst GE, Groener JE, Morava E, Wevers RA, Mannens M, Aerts JM, Meersseman W, Akkerman E, Niezen-Koning KE, Mulder MF, Visser G, Wijburg FA, Lefeber D, Poorthuis BJ. Hollak CE, et al. Among authors: visser g. Mol Genet Metab. 2012 Nov;107(3):526-33. doi: 10.1016/j.ymgme.2012.06.015. Epub 2012 Jun 30. Mol Genet Metab. 2012. PMID: 22818240

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