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	481.	Peroxisomal deficiencies are associated with altered activity of endothelial NOS in human fibroblasts. [electronic resource] by Koeck, T Kremser, K Producer: 20010809 In: Nitric oxide : biology and chemistry vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	482.	Inherited metabolic disorders presenting as hypoxic ischaemic encephalopathy: A case series of patients presenting at a tertiary care hospital in Pakistan. [electronic resource] by Zahid, Maya Khan, Aysha Habib Yunus, Zabedah Md Chen, Bee Chin Steinmann, Beat Johannes, Haberle Afroze, Bushra Producer: 20190807 In: JPMA. The Journal of the Pakistan Medical Association vol. 69 Availability: No items available. Save to lists Add to cart (remove)
	483.	Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7. [electronic resource] by Naritomi, K Izumikawa, Y Ohshiro, S Yoshida, K Shimozawa, N Suzuki, Y Orii, T Hirayama, K Producer: 19900209 In: Human genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	484.	A review of morphological techniques for detection of peroxisomal (and mitochondrial) proteins and their corresponding mRNAs during ontogenesis in mice: application to the PEX5-knockout mouse with Zellweger syndrome. [electronic resource] by Baumgart, Eveline Fahimi, H Dariush Steininger, Heike Grabenbauer, Markus Producer: 20030703 In: Microscopy research and technique vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	485.	PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G. [electronic resource] by Ghaedi, K Honsho, M Shimozawa, N Suzuki, Y Kondo, N Fujiki, Y Producer: 20001031 In: American journal of human genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	486.	Docosahexaenoic acid therapy in peroxisomal diseases: results of a double-blind, randomized trial. [electronic resource] by Paker, A M Sunness, J S Brereton, N H Speedie, L J Albanna, L Dharmaraj, S Moser, A B Jones, R O Raymond, G V Producer: 20100928 In: Neurology vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	487.	Mitochondrial adventures at the organelle society. [electronic resource] by Diogo, Cátia V Yambire, King Faisal Fernández Mosquera, Lorena Branco F, Tiago Raimundo, Nuno Producer: 20180906 In: Biochemical and biophysical research communications vol. 500 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	488.	Early dietary treatments with Lorenzo's oil and docosahexaenoic acid for neurological development in a case with Zellweger syndrome. [electronic resource] by Tanaka, Kyoko Shimizu, Toshiaki Ohtsuka, Yoshikazu Yamashiro, Yuichiro Oshida, Kyoichi Producer: 20071206 In: Brain & development vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	489.	Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata. [electronic resource] by Kanzawa, Noriyuki Shimozawa, Nobuyuki Wanders, Ronald J A Ikeda, Kazutaka Murakami, Yoshiko Waterham, Hans R Mukai, Satoru Fujita, Morihisa Maeda, Yusuke Taguchi, Ryo Fujiki, Yukio Kinoshita, Taroh Producer: 20120702 In: Journal of lipid research vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	490.	Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders. [electronic resource] by Martinez, M Producer: 19920918 In: Brain research vol. 583 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	491.	[Peroxisomes and neurologic diseases]. [electronic resource] by Sereni, C Paturneau-Jouas, M Producer: 19890804 In: Revue neurologique vol. 145 Availability: No items available. Save to lists Add to cart (remove)
	492.	Molecular analysis of peroxisomal beta-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect. [electronic resource] by Guerroui, S Aubourg, P Chen, W W Hashimoto, T Scotto, J Producer: 19890712 In: Biochemical and biophysical research communications vol. 161 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	493.	Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease. [electronic resource] by Baumgartner, M R Verhoeven, N M Jakobs, C Roels, F Espeel, M Martinez, M Rabier, D Wanders, R J Saudubray, J M Producer: 19981203 In: Neurology vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	494.	Immunochemical analysis of the peroxisomal beta-oxidation enzymes in rat and human heart and skeletal muscle and in skeletal muscle of Zellweger patients. [electronic resource] by Reubsaet, F A Brückwilder, M L Veerkamp, J H Trijbels, J M Hashimoto, T Monnens, L A Producer: 19911009 In: Biochemical medicine and metabolic biology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	495.	Late onset white matter disease in peroxisome biogenesis disorder. [electronic resource] by Barth, P G Gootjes, J Bode, H Vreken, P Majoie, C B Wanders, R J Producer: 20020115 In: Neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	496.	A human gene responsible for Zellweger syndrome that affects peroxisome assembly. [electronic resource] by Shimozawa, N Tsukamoto, T Suzuki, Y Orii, T Shirayoshi, Y Mori, T Fujiki, Y Producer: 19920415 In: Science (New York, N.Y.) vol. 255 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	497.	Inhibitors of COPI and COPII do not block PEX3-mediated peroxisome synthesis. [electronic resource] by South, S T Sacksteder, K A Li, X Liu, Y Gould, S J Producer: 20000801 In: The Journal of cell biology vol. 149 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	498.	Identification of a common PEX1 mutation in Zellweger syndrome. [electronic resource] by Collins, C S Gould, S J Producer: 19990921 In: Human mutation vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	499.	Evaluation of C26:0-lysophosphatidylcholine and C26:0-carnitine as diagnostic markers for Zellweger spectrum disorders. [electronic resource] by Klouwer, Femke C C Ferdinandusse, Sacha van Lenthe, Henk Kulik, Wim Wanders, Ronald J A Poll-The, Bwee Tien Waterham, Hans R Vaz, Frédéric M Producer: 20180607 In: Journal of inherited metabolic disease vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	500.	Blenderized Tube Feeding: Health Outcomes and Review of Homemade and Commercially Prepared Products. [electronic resource] by Bennett, Katherine Hjelmgren, Betsy Piazza, Jennifer Producer: 20210204 In: Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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