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	221.	[Cell biology from a medical viewpoint. XI. Peroxisomes: unmasking of a hidden organelle by studies of the Zellweger syndrome]. [electronic resource] by Wanders, R J Producer: 19920312 In: Nederlands tijdschrift voor geneeskunde vol. 136 Availability: No items available. Save to lists Add to cart (remove)
	222.	The pathology of peroxisomal disorders with pathogenetic considerations. [electronic resource] by Powers, J M Producer: 19951006 In: Journal of neuropathology and experimental neurology vol. 54 Availability: No items available. Save to lists Add to cart (remove)
	223.	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)
	224.	Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes. [electronic resource] by Tager, J M Brul, S Wiemer, E A Strijland, A Van Driel, R Schutgens, R B Van den Bosch, H Wanders, R J Westerveld, A Producer: 19900517 In: Progress in clinical and biological research vol. 321 Availability: No items available. Save to lists Add to cart (remove)
	225.	Ether lipid synthesis and its deficiency in peroxisomal disorders. [electronic resource] by van den Bosch, H Schrakamp, G Hardeman, D Zomer, A W Wanders, R J Schutgens, R B Producer: 19930709 In: Biochimie vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	226.	[Liver pathologies due to peroxisome disorders]. [electronic resource] by Lovisetto, P Raviolo, P Producer: 19940616 In: Recenti progressi in medicina vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	227.	Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome. [electronic resource] by Paton, B C Heron, S E Nelson, P V Morris, C P Poulos, A Producer: 19970710 In: American journal of human genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	228.	[Radiological quiz of the month]. [electronic resource] by Lienhardt, A Laroche, C Boncoeur, M P Maes, P Ronayette, D Boulesteix, J Producer: 19981020 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	229.	[Biogenesis of peroxisomes: analyses at molecular and cellular levels]. [electronic resource] by Fujiki, Y Miura, S Tsukamoto, T Producer: 19900827 In: Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	230.	Simultaneous enantioselective analysis of chiral urinary metabolites in patients with Zellweger syndrome. [electronic resource] by Muth, Alexandra Jung, Jochen Bilke, Steffi Scharrer, Annette Mosandl, Armin Sewell, Adrian C Böhles, Hans Producer: 20040324 In: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences vol. 792 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	231.	Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence. [electronic resource] by Cho, Sung Yoon Chang, Young Pyo Park, Ji Yun Park, Hyung-Doo Sohn, Young Bae Park, Sung Won Kim, Se Hwa Ji, Suntae Kim, Su Jin Choi, Eun Wha Kim, Chi Hwa Ko, Ah-ra Paik, Kyung-Hoon Jin, Dong-Kyu Producer: 20120125 In: Annals of clinical and laboratory science vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	232.	Clinical recognition of patients affected by a peroxisomal disorder: a retrospective study in 40 patients. [electronic resource] by Theil, A C Schutgens, R B Wanders, R J Heymans, H S Producer: 19920402 In: European journal of pediatrics vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	233.	Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts. [electronic resource] by Shimozawa, N Suzuki, Y Zhang, Z Imamura, A Kondo, N Kinoshita, N Fujiki, Y Tsukamoto, T Osumi, T Imanaka, T Orii, T Beemer, F Mooijer, P Dekker, C Wanders, R J Producer: 19990201 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	234.	Hospice support for families facing multiple deaths of children. [electronic resource] by Wolfe, J J Producer: 19971212 In: The American journal of hospice & palliative care vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	235.	High incidence of hyperoxaluria in generalized peroxisomal disorders. [electronic resource] by van Woerden, Christiaan S Groothoff, Jaap W Wijburg, Frits A Duran, Marinus Wanders, Ronald J A Barth, Peter G Poll-The, Bwee Tien Producer: 20060921 In: Molecular genetics and metabolism vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	236.	Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases. [electronic resource] by Suzuki, Y Shimozawa, N Yajima, S Yamaguchi, S Orii, T Hashimoto, T Producer: 19910315 In: Biochemical pharmacology vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	237.	[Peroxisomes and peroxisomal diseases]. [electronic resource] by Petelenz, M Gonciarz, Z Grzybek, H Panz, B Producer: 19911119 In: Postepy higieny i medycyny doswiadczalnej vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	238.	[Epilepsy due to inborn errors of metabolism]. [electronic resource] by Ito, Michinori Producer: 20030225 In: Ryoikibetsu shokogun shirizu no. 37 Pt 6 Availability: No items available. Save to lists Add to cart (remove)
	239.	Phytanic acid alpha-oxidation: decarboxylation of 2-hydroxyphytanoyl-CoA to pristanic acid in human liver. [electronic resource] by Verhoeven, N M Wanders, R J Schor, D S Jansen, G A Jakobs, C Producer: 19980121 In: Journal of lipid research vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	240.	[Neuronal migration disorders]. [electronic resource] by Vélez-Domínguez, L C Producer: 19980717 In: Gaceta medica de Mexico vol. 134 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 604 results.