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	1.	Hereditary porencephaly: clinical and MRI findings in two Dutch families. [electronic resource] by Mancini, G M S de Coo, I F M Lequin, M H Arts, W F Producer: 20040719 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease. [electronic resource] by Blok, M J Spruijt, L de Coo, I F M Schoonderwoerd, K Hendrickx, A Smeets, H J Producer: 20070514 In: Journal of medical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Lung disease in FLNA mutation: confirmatory report. [electronic resource] by de Wit, M C Y Tiddens, H A W M de Coo, I F M Mancini, G M S Producer: 20110928 In: European journal of medical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Movement disorder and neuronal migration disorder due to ARFGEF2 mutation. [electronic resource] by de Wit, M C Y de Coo, I F M Halley, D J J Lequin, M H Mancini, G M S Producer: 20091207 In: Neurogenetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The transmission of OXPHOS disease and methods to prevent this. [electronic resource] by Jacobs, L J A M de Wert, G Geraedts, J P M de Coo, I F M Smeets, H J M Producer: 20060405 In: Human reproduction update vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A simplified and reliable assay for complex I in human blood lymphocytes. [electronic resource] by de Wit, L E A Spruijt, L Schoonderwoerd, G C de Coo, I F M Smeets, H J M Scholte, H R Sluiter, W Producer: 20071030 In: Journal of immunological methods vol. 326 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	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)
	8.	Increased prevalences of left-handedness and left-eye sighting dominance in individuals with Williams-Beuren syndrome. [electronic resource] by Van Strien, J W Lagers-Van Haselen, G C Van Hagen, J M De Coo, I F M Frens, M A Van Der Geest, J N Producer: 20051130 In: Journal of clinical and experimental neuropsychology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects. [electronic resource] by de Wit, M C Y Kros, J M Halley, D J J de Coo, I F M Verdijk, R Jacobs, B C Mancini, G M S Producer: 20090420 In: Journal of neurology, neurosurgery, and psychiatry vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Is there alteration in aortic stiffness in Leber hereditary optic neuropathy? [electronic resource] by Nemes, A De Coo, I F M Spruijt, L Smeets, H J M Chinnery, P F Soliman, O I I Geleijnse, M L Ten Cate, F J Producer: 20080603 In: European journal of ophthalmology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Visual depth processing in Williams-Beuren syndrome. [electronic resource] by Van der Geest, J N Lagers-van Haselen, G C van Hagen, J M Brenner, E Govaerts, L C P de Coo, I F M Frens, M A Producer: 20060113 In: Experimental brain research vol. 166 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Absence epilepsy and periventricular nodular heterotopia. [electronic resource] by de Wit, M C Y Schippers, H M de Coo, I F M Arts, W F M Lequin, M H Brooks, A Visser, G H Mancini, G M S Producer: 20101202 In: Seizure vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) gene. [electronic resource] by van den Bosch, B J C de Coo, I F M Hendrickx, A T M Busch, H F M de Jong, G Scholte, H R Smeets, H J M Producer: 20041230 In: Neuromuscular disorders : NMD vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Saccade dysmetria in Williams-Beuren syndrome. [electronic resource] by van der Geest, J N Lagers-van Haselen, G C van Hagen, J M Govaerts, L C P de Coo, I F M de Zeeuw, C I Frens, M A Producer: 20040510 In: Neuropsychologia vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring. [electronic resource] by Hellebrekers, D M E I Wolfe, R Hendrickx, A T M de Coo, I F M de Die, C E Geraedts, J P M Chinnery, P F Smeets, H J M Producer: 20130923 In: Human reproduction update vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Decreased excitability of the distal motor nerve of young patients with type 1 diabetes mellitus. [electronic resource] by van der Heyden, Jc van der Meer, P Birnie, E de Coo, I F M Castro Cabezas, M Ozcan, B Veeze, Hj Visser, G H Aanstoot, H J Blok, J H Producer: 20140609 In: Pediatric diabetes vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus. [electronic resource] by de Wit, M C Y de Coo, I F M Julier, C Delépine, M Lequin, M H van de Laar, I Sibbles, B J Bruining, G J Mancini, G M S Producer: 20070912 In: Neurogenetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	How do changes in the mtDNA and mitochondrial dysfunction influence cancer and cancer therapy? Challenges, opportunities and models. [electronic resource] by van Gisbergen, M W Voets, A M Starmans, M H W de Coo, I F M Yadak, R Hoffmann, R F Boutros, P C Smeets, H J M Dubois, L Lambin, P Producer: 20150810 In: Mutation research. Reviews in mutation research vol. 764 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families. [electronic resource] by Mancini, G M S Catsman-Berrevoets, C E de Coo, I F M Aarsen, F K Kamphoven, J H J Huijmans, J G Duran, M van der Knaap, M S Jakobs, C Salomons, G S Producer: 20050315 In: American journal of medical genetics. Part A vol. 132A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Pearson syndrome and the role of deletion dimers and duplications in the mtDNA. [electronic resource] by Jacobs, L J A M Jongbloed, R J E Wijburg, F A de Klerk, J B C Geraedts, J P M Nijland, J G Scholte, H R de Coo, I F M Smeets, H J M Producer: 20041012 In: Journal of inherited metabolic disease vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 35 results.