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	341.	Propofol infusion syndrome or adrenoleukodystrophy? [electronic resource] by Karaman, Yucel Goktay, Aylin Agin, Hasan Karaarslan, Utku Producer: 20130830 In: Paediatric anaesthesia vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	342.	Biochemical markers predicting survival in peroxisome biogenesis disorders. [electronic resource] by Gootjes, J Mooijer, P A W Dekker, C Barth, P G Poll-The, B T Waterham, H R Wanders, R J A Producer: 20030110 In: Neurology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	343.	[Carrier state of x-linked adrenoleukodystrophy]. [electronic resource] by van Geel, B M Producer: 20001019 In: Nederlands tijdschrift voor geneeskunde vol. 144 Availability: No items available. Save to lists Add to cart (remove)
	344.	Atypical presentation of X-linked childhood adrenoleukodystrophy with an unusual magnetic resonance imaging pattern. [electronic resource] by Afifi, A K Menezes, A H Reed, L A Bell, W E Producer: 19970422 In: Journal of child neurology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	345.	Combined extraction of acyl carnitines and 26:0 lysophosphatidylcholine from dried blood spots: prospective newborn screening for X-linked adrenoleukodystrophy. [electronic resource] by Sandlers, Yana Moser, Ann B Hubbard, Walter C Kratz, Lisa E Jones, Richard O Raymond, Gerald V Producer: 20120716 In: Molecular genetics and metabolism vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	346.	Glucuronic acid-conjugated dihydroxy fatty acids in the urine of patients with generalized peroxisomal disorders. [electronic resource] by Street, J M Evans, J E Natowicz, M R Producer: 19960702 In: The Journal of biological chemistry vol. 271 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	347.	Rapid and quantitative analysis of unconjugated C(27) bile acids in plasma and blood samples by tandem mass spectrometry. [electronic resource] by Johnson, D W ten Brink, H J Schuit, R C Jakobs, C Producer: 20010628 In: Journal of lipid research vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	348.	Pristanic acid promotes oxidative stress in brain cortex of young rats: a possible pathophysiological mechanism for brain damage in peroxisomal disorders. [electronic resource] by Leipnitz, Guilhian Amaral, Alexandre Umpierrez Fernandes, Carolina Gonçalves Seminotti, Bianca Zanatta, Angela Knebel, Lisiane Aurélio Vargas, Carmen Regla Wajner, Moacir Producer: 20111115 In: Brain research vol. 1382 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	349.	Detection of unusual very-long-chain fatty acid and ether lipid derivatives in the fibroblasts and plasma of patients with peroxisomal diseases using liquid chromatography-mass spectrometry. [electronic resource] by Takashima, Shigeo Toyoshi, Kayoko Itoh, Takahiro Kajiwara, Naomi Honda, Ayako Ohba, Akiko Takemoto, Shoko Yoshida, Satoshi Shimozawa, Nobuyuki Producer: 20170829 In: Molecular genetics and metabolism vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	350.	Two polymorphic mutations (c2331A>C and IVS11+142insAGAAATTTTAAGTCTT) in the human peroxin 1 gene (PEX1). [electronic resource] by Preuss, N Gärtner, J Producer: 20010816 In: Human mutation vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	351.	Peroxisome biogenesis. [electronic resource] by Purdue, P E Lazarow, P B Producer: 20020115 In: Annual review of cell and developmental biology vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	352.	Peroxisomal disease cell lines with cellular plasmalogen deficiency have impaired muscarinic cholinergic signal transduction activity and amyloid precursor protein secretion. [electronic resource] by Périchon, R Moser, A B Wallace, W C Cunningham, S C Roth, G S Moser, H W Producer: 19980806 In: Biochemical and biophysical research communications vol. 248 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	353.	[Structural, functional and genetic aspects of peroxisome biogenesis]. [electronic resource] by Kurbatova, E M Dutova, T A Trotsenko, Iu A Producer: 20050715 In: Genetika vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	354.	Improved analysis of C26:0-lysophosphatidylcholine in dried-blood spots via negative ion mode HPLC-ESI-MS/MS for X-linked adrenoleukodystrophy newborn screening. [electronic resource] by Haynes, Christopher A De Jesús, Víctor R Producer: 20121105 In: Clinica chimica acta; international journal of clinical chemistry vol. 413 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	355.	Regulation of peroxisomal genes by DHEA and vitamin D. [electronic resource] by Depreter, Marianne Vandesompele, Jo Ferdinandusse, Sacha Speleman, Frank Roels, Frank 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)
	356.	Peroxisomal acyl-CoA synthetases. [electronic resource] by Watkins, Paul A Ellis, Jessica M Producer: 20130215 In: Biochimica et biophysica acta vol. 1822 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	357.	Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblasts. [electronic resource] by Wanders, R J Denis, S Ruiter, J P Schutgens, R B van Roermund, C W Jacobs, B S Producer: 19970313 In: Journal of inherited metabolic disease vol. 18 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	358.	Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13. [electronic resource] by Shimozawa, N Suzuki, Y Zhang, Z Imamura, A Tsukamoto, T Osumi, T Tateishi, K Okumoto, K Fujiki, Y Orii, T Barth, P G Wanders, R J Kondo, N Producer: 19980327 In: Biochemical and biophysical research communications vol. 243 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	359.	Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III. [electronic resource] by Okumoto, K Bogaki, A Tateishi, K Tsukamoto, T Osumi, T Shimozawa, N Suzuki, Y Orii, T Fujiki, Y Producer: 19970630 In: Experimental cell research vol. 233 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	360.	Peroxisome mosaics. [electronic resource] by Roels, Frank Saudubray, Jean-Marie Giros, Marisa Mandel, Hanna Eyskens, François Saracibar, Nieves Atares Pueyo, Begoña Prats, Jose M De Prest, Betty De Preter, Kathleen Pineda, Mercedes Krystkowiak, Pierre Gootjes, Jeannette Wanders, Ronald J A Espeel, Marc Poll-The, Bwee Tien 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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