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	1.	Lack of evidence of CD40 ligand involvement in transfusion-related acute lung injury. [electronic resource] by Tuinman, P R Gerards, M C Jongsma, G Vlaar, A P Boon, L Juffermans, N P Producer: 20110907 In: Clinical and experimental immunology vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Add-on treatment with intermediate-acting insulin versus sliding-scale insulin for patients with type 2 diabetes or insulin resistance during cyclic glucocorticoid-containing antineoplastic chemotherapy: a randomized crossover study. [electronic resource] by Gerards, M C de Maar, J S Steenbruggen, T G Hoekstra, J B L Vriesendorp, T M Gerdes, V E A Producer: 20171031 In: Diabetes, obesity & metabolism vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Comments on: Timing of operative treatment of fractures near the hip joint]. [electronic resource] by Gerards, M-G Haraszti, B Hess, J Houpert, A C D Idel, P D Klaeren, F N Krause, J Coburn, M Producer: 20190716 In: Der Anaesthesist vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Novel pathogenic SLC25A46 splice-site mutation causes an optic atrophy spectrum disorder. [electronic resource] by Nguyen, M Boesten, I Hellebrekers, D M E I Mulder-den Hartog, N M de Coo, I F M Smeets, H J M Gerards, M Producer: 20170613 In: Clinical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population. [electronic resource] by Bonneux, S Fransen, E Van Eyken, E Van Laer, L Huyghe, J Van de Heyning, P Voets, A Gerards, M Stassen, A P M Hendrickx, A T M Smeets, H J M Van Camp, G Producer: 20111201 In: Mitochondrion vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Defective NDUFA9 as a novel cause of neonatally fatal complex I disease. [electronic resource] by van den Bosch, B J C Gerards, M Sluiter, W Stegmann, A P A Jongen, E L C Hellebrekers, D M E I Oegema, R Lambrichs, E H Prokisch, H Danhauser, K Schoonderwoerd, K de Coo, I F M Smeets, H J M Producer: 20120410 In: Journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. [electronic resource] by Gerards, M Sluiter, W van den Bosch, B J C de Wit, L E A Calis, C M H Frentzen, M Akbari, H Schoonderwoerd, K Scholte, H R Jongbloed, R J Hendrickx, A T M de Coo, I F M Smeets, H J M Producer: 20101124 In: Journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)