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	221.	Complementation analysis in patients with the clinical phenotype of a generalised peroxisomal disorder. [electronic resource] by Steinberg, S J Fensom, A H Producer: 19960925 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	222.	[Congenital disorders of the bile acid metabolism (3 beta-hydroxy-delta 5-steroid dehydrogenase/isomerase deficiency, delta 4-3-oxosteroid 5 beta-reductase deficiency, cerebrotendinous xanthomatosis, and peroxisomal disorders]. [electronic resource] by Kondo, K H Maeda, Y Setoguchi, T Producer: 19960318 In: Ryoikibetsu shokogun shirizu no. 8 Availability: No items available. Save to lists Add to cart (remove)
	223.	Analysis of the putative role of 24-carbon polyunsaturated fatty acids in the biosynthesis of docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids. [electronic resource] by Infante, J P Huszagh, V A Producer: 19980806 In: FEBS letters vol. 431 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	224.	Hepatocyte transplantation in a 4-year-old girl with peroxisomal biogenesis disease: technique, safety, and metabolic follow-up. [electronic resource] by Sokal, Etienne M Smets, Françoise Bourgois, Annick Van Maldergem, Lionel Buts, Jean-Paul Reding, Raymond Bernard Otte, Jean Evrard, Veerle Latinne, Dominique Vincent, Marie Françoise Moser, Anne Soriano, Humberto E Producer: 20031002 In: Transplantation vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	225.	Stereochemistry of the peroxisomal branched-chain fatty acid alpha- and beta-oxidation systems in patients suffering from different peroxisomal disorders. [electronic resource] by Ferdinandusse, S Rusch, H van Lint, A E M Dacremont, G Wanders, R J A Vreken, P Producer: 20020625 In: Journal of lipid research vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	226.	Peroxisomal Membrane and Matrix Protein Import Using a Semi-Intact Mammalian Cell System. [electronic resource] by Okumoto, Kanji Honsho, Masanori Liu, Yuqiong Fujiki, Yukio Producer: 20170518 In: Methods in molecular biology (Clifton, N.J.) vol. 1595 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	227.	Peroxisome-targeted Supramolecular Nanoprobes Assembled with Pyrene-labelled Peptide Amphiphiles. [electronic resource] by Kim, Inhye Bang, Woo-Young Kim, Sooyong Jin, Seon-Mi Hyun, Ju-Yong Han, Eun Hee Lee, Eunji Producer: 20181211 In: Chemistry, an Asian journal vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	228.	Modeling human peroxisome biogenesis disorders in the nematode Caenorhabditis elegans. [electronic resource] by Thieringer, Heather Moellers, Britta Dodt, Gabriele Kunau, Wolf-H Driscoll, Monica Producer: 20040123 In: Journal of cell science vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	229.	[Peroxisome biogenesis and human disorders]. [electronic resource] by Fujiki, Y Okumoto, K Producer: 20000711 In: Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	230.	Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. [electronic resource] by Shimozawa, Nobuyuki Nagase, Tomoko Takemoto, Yasuhiko Suzuki, Yasuyuki Kondo, Naomi Producer: 20040702 In: Advances in experimental medicine and biology vol. 544 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	231.	Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse. [electronic resource] by Wangler, Michael F Chao, Yu-Hsin Bayat, Vafa Giagtzoglou, Nikolaos Shinde, Abhijit Babaji Putluri, Nagireddy Coarfa, Cristian Donti, Taraka Graham, Brett H Faust, Joseph E McNew, James A Moser, Ann Sardiello, Marco Baes, Myriam Bellen, Hugo J Producer: 20170706 In: PLoS genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	232.	Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease. [electronic resource] by Geisbrecht, B V Collins, C S Reuber, B E Gould, S J Producer: 19980820 In: Proceedings of the National Academy of Sciences of the United States of America vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	233.	A rapid screening procedure for the diagnosis of peroxisomal disorders: quantification of very long-chain fatty acids, as dimethylaminoethyl esters, in plasma and blood spots, by electrospray tandem mass spectrometry. [electronic resource] by Johnson, D W Producer: 20010111 In: Journal of inherited metabolic disease vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	234.	[Adult-onset metabolic diseases]. [electronic resource] by García Ribes, A Martínez González, Mj García Cazorla, A Producer: 20090202 In: Anales del sistema sanitario de Navarra vol. 31 Suppl 2 Availability: No items available. Save to lists Add to cart (remove)
	235.	Newborn screening for lysosomal storage disorders and other neuronopathic conditions. [electronic resource] by Matern, Dietrich Oglesbee, Devin Tortorelli, Silvia Producer: 20140317 In: Developmental disabilities research reviews vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	236.	Pendular nystagmus in patients with peroxisomal assembly disorder. [electronic resource] by Kori, A A Robin, N H Jacobs, J B Erchul, D M Zaidat, O O Remler, B F Averbuch-Heller, L Dell'Osso, L F Leigh, R J Zinn, A B Producer: 19980506 In: Archives of neurology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	237.	Metabolic and molecular basis of peroxisomal disorders: a review. [electronic resource] by Wanders, Ronald J A Producer: 20041019 In: American journal of medical genetics. Part A vol. 126A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	238.	Interval spectral-domain optical coherence tomography and electrophysiology findings in neonatal adrenoleukodystrophy. [electronic resource] by Courtney, Robert J Pennesi, Mark E Producer: 20130816 In: JAMA ophthalmology vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	239.	Relapsing rhabdomyolysis due to peroxisomal alpha-methylacyl-coa racemase deficiency. [electronic resource] by Kapina, V Sedel, F Truffert, A Horvath, J Wanders, R J A Waterham, H R Picard, F Producer: 20101022 In: Neurology vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	240.	Peroxisomes in dermatology. Part I. [electronic resource] by Smith, K J Dipreta, E Skelton, H Producer: 20011204 In: Journal of cutaneous medicine and surgery vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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