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	361.	Hepatic symptoms and histology in 13 patients with a Zellweger spectrum disorder. [electronic resource] by Berendse, Kevin Koot, Bart G P Klouwer, Femke C C Engelen, Marc Roels, Frank Lacle, Miangela M Nikkels, Peter G J Verheij, Joanne Poll-The, Bwee Tien Producer: 20200916 In: Journal of inherited metabolic disease vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	362.	Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts. [electronic resource] by Verhoeven, N M Roe, D S Kok, R M Wanders, R J Jakobs, C Roe, C R Producer: 19980326 In: Journal of lipid research vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	363.	Peroxisomal ghosts are intracellular structures distinct from lysosomal compartments in Zellweger syndrome: a confocal laser scanning microscopy study. [electronic resource] by Santos, M J Henderson, S C Moser, A B Moser, H W Lazarow, P B Producer: 20001019 In: Biology of the cell vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	364.	[Farnesoid X receptor(FXR)]. [electronic resource] by Fujii, H Producer: 20010927 In: Nihon rinsho. Japanese journal of clinical medicine vol. 59 Suppl 2 Availability: No items available. Save to lists Add to cart (remove)
	365.	Stereoselective analysis of 2-hydroxysebacic acid in urine of patients with Zellweger syndrome and of premature infants fed with medium-chain triglycerides. [electronic resource] by Muth, A Mosandl, A Wanders, R J A Nowaczyk, M J M Baric, I Böhles, H Sewell, A C Producer: 20040617 In: Journal of inherited metabolic disease vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	366.	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)
	367.	Very long-chain fatty acids in peroxisomal disease. [electronic resource] by Poulos, A Beckman, K Johnson, D W Paton, B C Robinson, B S Sharp, P Usher, S Singh, H Producer: 19920826 In: Advances in experimental medicine and biology vol. 318 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	368.	A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities. [electronic resource] by Wanders, R J van Roermund, C W Schelen, A Schutgens, R B Tager, J M Stephenson, J B Clayton, P T Producer: 19901212 In: Journal of inherited metabolic disease vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	369.	Transport of microinjected proteins into peroxisomes of mammalian cells: inability of Zellweger cell lines to import proteins with the SKL tripeptide peroxisomal targeting signal. [electronic resource] by Walton, P A Gould, S J Feramisco, J R Subramani, S Producer: 19920224 In: Molecular and cellular biology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	370.	The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum. [electronic resource] by Steinberg, Steven Chen, Li Wei, Liumei Moser, Ann Moser, Hugo Cutting, Garry Braverman, Nancy Producer: 20050318 In: Molecular genetics and metabolism vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	371.	[Biogenesis of peroxisome--targeting signal and peroxisome assembly factor]. [electronic resource] by Fujiki, Y Producer: 19920528 In: No to hattatsu = Brain and development vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	372.	The optimized use of gas chromatography-mass spectrometry and high performance liquid chromatography to analyse the serum bile acids of patients with metabolic cholestasis and peroxisomal disorders. [electronic resource] by Courillon, F Gerhardt, M F Myara, A Rocchiccioli, F Trivin, F Producer: 19980403 In: European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	373.	Clinical approach to inherited peroxisomal disorders: a series of 27 patients. [electronic resource] by Baumgartner, M R Poll-The, B T Verhoeven, N M Jakobs, C Espeel, M Roels, F Rabier, D Levade, T Rolland, M O Martinez, M Wanders, R J Saudubray, J M Producer: 19981202 In: Annals of neurology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	374.	The cholic acid extension study in Zellweger spectrum disorders: Results and implications for therapy. [electronic resource] by Klouwer, Femke C C Koot, Bart G P Berendse, Kevin Kemper, Elles M Ferdinandusse, Sacha Koelfat, Kiran V K Lenicek, Martin Vaz, Frédéric M Engelen, Marc Jansen, Peter L M Wanders, Ronald J A Waterham, Hans R Schaap, Frank G Poll-The, Bwee Tien Producer: 20200618 In: Journal of inherited metabolic disease vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	375.	[Human peroxisome-deficient disorders and pathogenic gene]. [electronic resource] by Fujiki, Y Producer: 19950711 In: Rinsho shinkeigaku = Clinical neurology vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	376.	Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients. [electronic resource] by Thoms, Sven Grønborg, Sabine Rabenau, Jana Ohlenbusch, Andreas Rosewich, Hendrik Gärtner, Jutta Producer: 20111026 In: BMC medical genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	377.	Development and validation of a severity scoring system for Zellweger spectrum disorders. [electronic resource] by Klouwer, F C C Meester-Delver, A Vaz, F M Waterham, H R Hennekam, R C M Poll-The, B T Producer: 20190911 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	378.	Severe changes in polyunsaturated fatty acids in the brain, liver, kidney, and retina in patients with peroxisomal disorders. [electronic resource] by Martinez, M Producer: 19920826 In: Advances in experimental medicine and biology vol. 318 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	379.	Abnormal expression of cell adhesion molecule L1 in migration disorders: a developmental immunohistochemical study. [electronic resource] by Tsuru, A Mizuguchi, M Uyemura, K Takashima, S Producer: 19970806 In: Clinical neuropathology vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	380.	The use of automated electrospray ionization tandem MS for the diagnosis of inborn errors of metabolism from dried blood spots. [electronic resource] by Johnson, A W Mills, K Clayton, P T Producer: 19970226 In: Biochemical Society transactions vol. 24 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 604 results.