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	1.	How to use acylcarnitine profiles to help diagnose inborn errors of metabolism. [electronic resource] by Santra, S Hendriksz, C Producer: 20110107 In: Archives of disease in childhood. Education and practice edition vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Feeding infants with undiluted goat's milk can mimic tyrosinaemia type 1. [electronic resource] by Hendriksz, C J Walter, J H Producer: 20040901 In: Acta paediatrica (Oslo, Norway : 1992) vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Objective results of median nerve decompression and tenosynovectomy for carpal tunnel syndrome in patients with mucopolysaccharidoses Types I and II. [electronic resource] by Aslam, R Hendriksz, C J Jester, A Producer: 20151015 In: The Journal of hand surgery, European volume vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Successful pregnancy in a treated patient with biotinidase deficiency. [electronic resource] by Hendriksz, C J Preece, M A Chakrapani, A Producer: 20060130 In: Journal of inherited metabolic disease vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Pregnancy in a patient with mucopolysaccharidosis type IH homozygous for the W402X mutation. [electronic resource] by Hendriksz, C J Moss, G M Wraith, J E Producer: 20050324 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)
	6.	Homozygous hypercholesterolaemia and ezetimibe: a case report. [electronic resource] by Hendriksz, C J Norbury, G Tabrah, S Taylor, A Humphries, S E Producer: 20040614 In: Acta paediatrica (Oslo, Norway : 1992) vol. 93 Availability: No items available. Save to lists Add to cart (remove)
	7.	Prospective treatment in carnitine-acylcarnitine translocase deficiency. [electronic resource] by Pierre, G Macdonald, A Gray, G Hendriksz, C Preece, M A Chakrapani, A Producer: 20071025 In: Journal of inherited metabolic disease vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Home delivery of dietary products in inherited metabolic disorders reduces prescription and dispensing errors. [electronic resource] by MacDonald, A Manji, N Evans, S Davies, P Daly, A Hendriksz, C Chakrapani, A Producer: 20070109 In: Journal of human nutrition and dietetics : the official journal of the British Dietetic Association vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Intellectual and neurological functioning in Morquio syndrome (MPS IVa). [electronic resource] by Davison, J E Kearney, S Horton, J Foster, K Peet, A C Hendriksz, C J Producer: 20140114 In: Journal of inherited metabolic disease vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Loss of NPC1 function in a patient with a co-inherited novel insulin receptor mutation does not grossly modify the severity of the associated insulin resistance. [electronic resource] by Kirk, J Porter, K M Parker, V Barroso, I O'Rahilly, S Hendriksz, C Semple, R K Producer: 20140408 In: Journal of inherited metabolic disease vol. 33 Suppl 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Breast feeding in IMD. [electronic resource] by MacDonald, A Depondt, E Evans, S Daly, A Hendriksz, C Chakrapani A, A Saudubray, J-M Producer: 20070109 In: Journal of inherited metabolic disease vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Protein substitute dosage in PKU: how much do young patients need? [electronic resource] by MacDonald, A Chakrapani, A Hendriksz, C Daly, A Davies, P Asplin, D Hall, K Booth, I W Producer: 20060721 In: Archives of disease in childhood vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Does maternal knowledge and parent education affect blood phenylalanine control in phenylketonuria? [electronic resource] by Macdonald, A Davies, P Daly, A Hopkins, V Hall, S K Asplin, D Hendriksz, C Chakrapani, A Producer: 20081128 In: Journal of human nutrition and dietetics : the official journal of the British Dietetic Association vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Juvenile Sandhoff disease--nine new cases and a review of the literature. [electronic resource] by Hendriksz, C J Corry, P C Wraith, J E Besley, G T N Cooper, A Ferrie, C D Producer: 20041230 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)
	15.	Dietary practices in glutaric aciduria type 1 over 16 years. [electronic resource] by Gokmen-Ozel, H MacDonald, A Daly, A Ashmore, C Preece, M A Hendriksz, C Vijay, S Chakrapani, A Producer: 20130424 In: Journal of human nutrition and dietetics : the official journal of the British Dietetic Association vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	'Ready to drink' protein substitute is easier is for people with phenylketonuria. [electronic resource] by MacDonald, A Lilburn, M Davies, P Evans, S Daly, A Hall, S K Hendriksz, C Chakrapani, A Lee, P Producer: 20070108 In: Journal of inherited metabolic disease vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Review of clinical presentation and diagnosis of mucopolysaccharidosis IVA. [electronic resource] by Hendriksz, C J Harmatz, P Beck, M Jones, S Wood, T Lachman, R Gravance, C G Orii, T Tomatsu, S Producer: 20140317 In: Molecular genetics and metabolism vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Long-term compliance with a novel vitamin and mineral supplement in older people with PKU. [electronic resource] by MacDonald, A Lee, P Davies, P Daly, A Lilburn, M Gokmen Ozel, H Preece, M A Hendriksz, C Chakrapani, A Producer: 20090424 In: Journal of inherited metabolic disease vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannose. [electronic resource] by Hendriksz, C J McClean, P Henderson, M J Keir, D G Worthington, V C Imtiaz, F Schollen, E Matthijs, G Winchester, B G Producer: 20011004 In: Archives of disease in childhood vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Development of a suspicion index to aid diagnosis of Niemann-Pick disease type C. [electronic resource] by Wijburg, F A Sedel, F Pineda, M Hendriksz, C J Fahey, M Walterfang, M Patterson, M C Wraith, J E Kolb, S A Producer: 20120709 In: Neurology vol. 78 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 27 results.