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	161.	Zellweger syndrome, retinal involvement. [electronic resource] by Stanesu-Segal, B Evrard, P Producer: 19900425 In: Metabolic, pediatric, and systemic ophthalmology (New York, N.Y. : 1985) vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	162.	New disorders of neurometabolism: when and how to investigate them. [electronic resource] by Haan, E A Producer: 19890309 In: Australian paediatric journal vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	163.	Ependymal abnormalities in cerebro-hepato-renal disease of Zellweger. [electronic resource] by Sarnat, H B Trevenen, C L Darwish, H Z Producer: 19931229 In: Brain & development vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	164.	Phytanic acid oxidation in man: identification of a new enzyme catalysing the formation of 2-ketophytanic acid from 2-hydroxyphytanic acid and its deficiency in the Zellweger syndrome. [electronic resource] by Wanders, R J van Roermund, C W Schor, D S ten Brink, H J Jakobs, C Producer: 19951122 In: Journal of inherited metabolic disease vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	165.	Rapid prenatal diagnosis of fetal Zellweger syndrome by biochemical tests, complementation studies, and molecular analyses. [electronic resource] by Segers, Karin Pierquin, Genevieve Gaillez, Stephanie Delbecque, Katty Retz, Maria Tebache, Malek Waterham, Hans Wanders, Ronald Ferdinandusse, Sacha Debray, François-Guillaume Producer: 20130902 In: Prenatal diagnosis vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	166.	A deleterious mutation in the PEX2 gene causes Zellweger syndrome in individuals of Ashkenazi Jewish descent. [electronic resource] by Fedick, A Jalas, C Treff, N R Producer: 20150512 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	167.	A comparative study of straight chain and branched chain fatty acid oxidation in skin fibroblasts from patients with peroxisomal disorders. [electronic resource] by Singh, H Usher, S Johnson, D Poulos, A Producer: 19900524 In: Journal of lipid research vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	168.	[Peroxisomes and neurological disorders]. [electronic resource] by Suzuki, Y Yamaguchi, S Orii, T Producer: 19901207 In: No to shinkei = Brain and nerve vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	169.	[Specialized roles of mitochondria and peroxisomes in fatty acid oxidation]. [electronic resource] by Hashimoto, T Producer: 19950221 In: Seikagaku. The Journal of Japanese Biochemical Society vol. 66 Availability: No items available. Save to lists Add to cart (remove)
	170.	Molecular species of phospholipids with very long chain fatty acids in skin fibroblasts of Zellweger syndrome. [electronic resource] by Hama, Kotaro Nagai, Toru Nishizawa, Chiho Ikeda, Kazutaka Morita, Masashi Satoh, Noriko Nakanishi, Hiroki Imanaka, Tsuneo Shimozawa, Nobuyuki Taguchi, Ryo Inoue, Keizo Yokoyama, Kazuaki Producer: 20140813 In: Lipids vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	171.	First Japanese case of Zellweger syndrome with a mutation in PEX14. [electronic resource] by Komatsuzaki, Shoko Ogawa, Eishin Shimozawa, Nobuyuki Sakamoto, Osamu Haginoya, Kazuhiro Uematsu, Mitsugu Hasegawa, Yuki Matsubara, Yoichi Ohura, Toshihiro Producer: 20170117 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	172.	The peroxisome and the eye. [electronic resource] by Folz, S J Trobe, J D Producer: 19910703 In: Survey of ophthalmology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	173.	Low-density particles (W-particles) containing catalase in Zellweger syndrome and normal fibroblasts. [electronic resource] by Aikawa, J Chen, W W Kelley, R I Tada, K Moser, H W Chen, G L Producer: 19911226 In: Proceedings of the National Academy of Sciences of the United States of America vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	174.	Additional congenital defects in anorectal malformations. [electronic resource] by Hassink, E A Rieu, P N Hamel, B C Severijnen, R S vd Staak, F H Festen, C Producer: 19961206 In: European journal of pediatrics vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	175.	[Zellweger syndrome, neonatal adrenoleukodystrophy or infantile Refsum's disease in a case with generalized peroxisome defect?]. [electronic resource] by Schmitt, K Molzer, B Stöckler, S Tulzer, G Tulzer, W Producer: 19930819 In: Wiener klinische Wochenschrift vol. 105 Availability: No items available. Save to lists Add to cart (remove)
	176.	The Zellweger syndrome: deficient conversion of docosahexaenoic acid (22:6(n-3)) to eicosapentaenoic acid (20:5(n-3)) and normal delta 4-desaturase activity in cultured skin fibroblasts. [electronic resource] by Grønn, M Christensen, E Hagve, T A Christophersen, B O Producer: 19900702 In: Biochimica et biophysica acta vol. 1044 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	177.	Protein kinase C activity, phosphate uptake and endogenous substrate phosphorylation are altered in Zellweger syndrome. [electronic resource] by Boneh, A Producer: 19970303 In: Journal of inherited metabolic disease vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	178.	Biochemical features of a patient with Zellweger-like syndrome with normal PTS-1 and PTS-2 peroxisomal protein import systems: a new peroxisomal disease. [electronic resource] by Singh, I Voigt, R G Sheikh, F G Kremser, K Brown, F R Producer: 19971023 In: Biochemical and molecular medicine vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	179.	Zellweger syndrome - a lethal peroxisome biogenesis disorder. [electronic resource] by Rafique, Muhammad Zia, Shumaila Rana, Muhammad Nasir Mostafa, Ossama A Producer: 20130806 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	180.	Essential fatty acids and serine as plasmalogen precursors in relation to competing metabolic pathways. [electronic resource] by Cook, H W Thomas, S E Xu, Z Producer: 19920406 In: Biochemistry and cell biology = Biochimie et biologie cellulaire vol. 69 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 604 results.