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Year | Number of Results |
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2009 | 1 |
2010 | 1 |
2012 | 1 |
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2014 | 2 |
2024 | 0 |
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Page 1
Detection of pulmonary complications in common variable immunodeficiency.
Pediatr Allergy Immunol. 2010 Aug;21(5):793-805. doi: 10.1111/j.1399-3038.2009.00963.x. Epub 2009 Nov 13.
Pediatr Allergy Immunol. 2010.
PMID: 19912551
Review.
From genome to phenome-Simple inborn errors of metabolism as complex traits.
Touw CM, Derks TG, Bakker BM, Groen AK, Smit GP, Reijngoud DJ.
Touw CM, et al.
Biochim Biophys Acta. 2014 Oct;1842(10):2021-2029. doi: 10.1016/j.bbadis.2014.05.032. Epub 2014 Jun 3.
Biochim Biophys Acta. 2014.
PMID: 24905735
Free article.
Review.
Item in Clipboard
Biochemical competition makes fatty-acid β-oxidation vulnerable to substrate overload.
van Eunen K, Simons SM, Gerding A, Bleeker A, den Besten G, Touw CM, Houten SM, Groen BK, Krab K, Reijngoud DJ, Bakker BM.
van Eunen K, et al. Among authors: touw cm.
PLoS Comput Biol. 2013;9(8):e1003186. doi: 10.1371/journal.pcbi.1003186. Epub 2013 Aug 15.
PLoS Comput Biol. 2013.
PMID: 23966849
Free PMC article.
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Clinical pathways for inborn errors of metabolism: warranted and feasible.
Demirdas S, van Kessel IN, Korndewal MJ, Hollak CE, Meutgeert H, Klaren A, van Rijn M, van Spronsen FJ, Bosch AM; Dutch working Group.
Demirdas S, et al.
Orphanet J Rare Dis. 2013 Feb 25;8:37. doi: 10.1186/1750-1172-8-37.
Orphanet J Rare Dis. 2013.
PMID: 23442887
Free PMC article.
Item in Clipboard
In vitro and in vivo consequences of variant medium-chain acyl-CoA dehydrogenase genotypes.
Touw CM, Smit GP, Niezen-Koning KE, Bosgraaf-de Boer C, Gerding A, Reijngoud DJ, Derks TG.
Touw CM, et al.
Orphanet J Rare Dis. 2013 Mar 20;8:43. doi: 10.1186/1750-1172-8-43.
Orphanet J Rare Dis. 2013.
PMID: 23509891
Free PMC article.
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Experimental evidence for protein oxidative damage and altered antioxidant defense in patients with medium-chain acyl-CoA dehydrogenase deficiency.
Derks TG, Touw CM, Ribas GS, Biancini GB, Vanzin CS, Negretto G, Mescka CP, Reijngoud DJ, Smit GP, Wajner M, Vargas CR.
Derks TG, et al. Among authors: touw cm.
J Inherit Metab Dis. 2014 Sep;37(5):783-9. doi: 10.1007/s10545-014-9700-0. Epub 2014 Mar 13.
J Inherit Metab Dis. 2014.
PMID: 24623196
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Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study.
Touw CM, Smit GP, de Vries M, de Klerk JB, Bosch AM, Visser G, Mulder MF, Rubio-Gozalbo ME, Elvers B, Niezen-Koning KE, Wanders RJ, Waterham HR, Reijngoud DJ, Derks TG.
Touw CM, et al.
Orphanet J Rare Dis. 2012 May 25;7:30. doi: 10.1186/1750-1172-7-30.
Orphanet J Rare Dis. 2012.
PMID: 22630369
Free PMC article.
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