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	481.	Orthotopic liver transplantation from a living-related donor in an infant with a peroxisome biogenesis defect of the infantile Refsum disease type. [electronic resource] by Van Maldergem, L Moser, A B Vincent, M-F Roland, D Reding, R Otte, J-B Wanders, R J Sokal, E Producer: 20050915 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)
	482.	Peroxisomes control mitochondrial dynamics and the mitochondrion-dependent apoptosis pathway. [electronic resource] by Tanaka, Hideaki Okazaki, Tomohiko Aoyama, Saeko Yokota, Mutsumi Koike, Masato Okada, Yasushi Fujiki, Yukio Gotoh, Yukiko Producer: 20200629 In: Journal of cell science vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	483.	Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency. [electronic resource] by Ferdinandusse, Sacha Denis, Simone Hogenhout, Eveline M Koster, Janet van Roermund, Carlo W T IJlst, Lodewijk Moser, Ann B Wanders, Ronald J A Waterham, Hans R Producer: 20071002 In: Human mutation vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	484.	Human disorders of peroxisome metabolism and biogenesis. [electronic resource] by Waterham, Hans R Ferdinandusse, Sacha Wanders, Ronald J A Producer: 20160607 In: Biochimica et biophysica acta vol. 1863 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	485.	Peroxisomal multifunctional protein-2 deficiency causes motor deficits and glial lesions in the adult central nervous system. [electronic resource] by Huyghe, Steven Schmalbruch, Henning Hulshagen, Leen Veldhoven, Paul Van Baes, Myriam Hartmann, Dieter Producer: 20060525 In: The American journal of pathology vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	486.	Neuronal and glial accumulation of alpha- and beta-synucleins in human lipidoses. [electronic resource] by Suzuki, Kyoko Iseki, Eizo Togo, Takashi Yamaguchi, Akira Katsuse, Omi Katsuyama, Kayoko Kanzaki, Seiichi Shiozaki, Kazumasa Kawanishi, Chiaki Yamashita, Sumimasa Tanaka, Yukichi Yamanaka, Shoji Hirayasu, Yoshio Producer: 20080219 In: Acta neuropathologica vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	487.	A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β gene. [electronic resource] by Ebberink, Merel S Koster, Janet Visser, Gepke Spronsen, Francjan van Stolte-Dijkstra, Irene Smit, G Peter A Fock, Johanna M Kemp, Stephan Wanders, Ronald J A Waterham, Hans R Producer: 20121119 In: Journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	488.	Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders. [electronic resource] by Imamura, A Tamura, S Shimozawa, N Suzuki, Y Zhang, Z Tsukamoto, T Orii, T Kondo, N Osumi, T Fujiki, Y Producer: 19990121 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	489.	Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency. [electronic resource] by van Grunsven, E G Mooijer, P A Aubourg, P Wanders, R J Producer: 19990914 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	490.	Correlative value of magnetic resonance imaging for neurodevelopmental outcome in periventricular leukomalacia. [electronic resource] by Serdaroglu, Gul Tekgul, Hasan Kitis, Omer Serdaroglu, Erkin Gökben, Sarenur Producer: 20041202 In: Developmental medicine and child neurology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	491.	Amnioinfusion for relief of recurrent severe and moderate variable decelerations in labor. [electronic resource] by Regi, Annie Alexander, Nancy Jose, Ruby Lionel, Jessie Varghese, Lilly Peedicayil, Abraham Producer: 20090709 In: The Journal of reproductive medicine vol. 54 Availability: No items available. Save to lists Add to cart (remove)
	492.	Proton magnetic resonance spectroscopy (1H-MRS) of the cerebrum in two young infants with Zellweger syndrome. [electronic resource] by Groenendaal, F Bianchi, M C Battini, R Tosetti, M Boldrini, A de Vries, L S Cioni, G Producer: 20010920 In: Neuropediatrics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	493.	Tremor and deep white matter changes in alpha-methylacyl-CoA racemase deficiency. [electronic resource] by Clarke, C E Alger, S Preece, M A Burdon, M A Chavda, S Denis, S Ferdinandusse, S Wanders, R J A Producer: 20041221 In: Neurology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	494.	The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor. [electronic resource] by Yahraus, T Braverman, N Dodt, G Kalish, J E Morrell, J C Moser, H W Valle, D Gould, S J Producer: 19960827 In: The EMBO journal vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	495.	Impaired membrane traffic in defective ether lipid biosynthesis. [electronic resource] by Thai, T P Rodemer, C Jauch, A Hunziker, A Moser, A Gorgas, K Just, W W Producer: 20010315 In: Human molecular genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	496.	[Inborn metabolic diseases--rare, but nevertheless common]. [electronic resource] by Nordenström, Anna von Döbeln, Ulrika Producer: 20101210 In: Lakartidningen vol. 107 Availability: No items available. Save to lists Add to cart (remove)
	497.	Determination of plasma pipecolic acid by an easy and rapid liquid chromatography-tandem mass spectrometry method. [electronic resource] by Semeraro, Michela Muraca, Maurizio Catesini, Giulio Inglese, Rita Iacovone, Francesca Barraco, Gloria Maria Manco, Melania Boenzi, Sara Dionisi-Vici, Carlo Rizzo, Cristiano Producer: 20151005 In: Clinica chimica acta; international journal of clinical chemistry vol. 440 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	498.	Predicting the function and subcellular location of Caenorhabditis elegans proteins similar to Saccharomyces cerevisiae beta-oxidation enzymes. [electronic resource] by Gurvitz, A Langer, S Piskacek, M Hamilton, B Ruis, H Hartig, A Producer: 20001128 In: Yeast (Chichester, England) vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	499.	Peroxisomal bifunctional enzyme deficiency with associated retinal findings. [electronic resource] by Al-Hazzaa, S A Ozand, P T Producer: 19970916 In: Ophthalmic genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	500.	Lessons from knockout mice. I: Phenotypes of mice with peroxisome biogenesis disorders. [electronic resource] by Baes, Myriam Van Veldhoven, Paul P 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)

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Your search returned 571 results.