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	121.	Rapid analysis of conjugated bile acids in plasma using electrospray tandem mass spectrometry: application for selective screening of peroxisomal disorders. [electronic resource] by Bootsma, A H Overmars, H van Rooij, A van Lint, A E Wanders, R J van Gennip, A H Vreken, P Producer: 19990910 In: Journal of inherited metabolic disease vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	122.	"Role of peroxisomes in human lipid metabolism and its importance for neurological development". [electronic resource] by Wanders, Ronald J A Poll-The, Bwee Tien Producer: 20171031 In: Neuroscience letters vol. 637 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	Chondrodysplasia punctatas and the peroxisomopathies: overlapping syndrome communities. [electronic resource] by Wilson, G N Holmes, R D Hajra, A K Producer: 19890316 In: Pathology and immunopathology research vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	124.	MR in a patient with Zellweger syndrome presenting without cortical or myelination abnormalities. [electronic resource] by Stone, J A Castillo, M Producer: 19981118 In: AJNR. American journal of neuroradiology vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	125.	Enhanced expression of a-series gangliosides in fibroblasts of patients with peroxisome biogenesis disorders. [electronic resource] by Tatsumi, K Saito, M Lin, B Iwamori, M Ichiseki, H Shimozawa, N Kamoshita, S Igarashi, T Sakakihara, Y Producer: 20010517 In: Biochimica et biophysica acta vol. 1535 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Zellweger syndrome with severe malnutrition, immunocompromised state and opportunistic infections. [electronic resource] by Cardoso, Patrícia Amaral, Maria Emanuel Lemos, Sónia Garcia, Paula Producer: 20170104 In: BMJ case reports vol. 2016 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	127.	A Genetic Screen for Genes That Impact Peroxisomes in [electronic resource] by Graves, Hillary K Jangam, Sharayu Tan, Kai Li Pignata, Antonella Seto, Elaine S Yamamoto, Shinya Wangler, Michael F Producer: 20200608 In: G3 (Bethesda, Md.) vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	[Diseases and developmental disorders caused by mutations in genes encoding AAA and AAA+ proteins]. [electronic resource] by Ogura, T Producer: 20011211 In: Seikagaku. The Journal of Japanese Biochemical Society vol. 73 Availability: No items available. Save to lists Add to cart (remove)
	129.	Rational diagnostic strategy for Zellweger syndrome spectrum patients. [electronic resource] by Krause, Cindy Rosewich, Hendrik Gärtner, Jutta Producer: 20090901 In: European journal of human genetics : EJHG vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	Absence of biochemical evidence at an early age delays diagnosis in a patient with a clinically severe peroxisomal biogenesis disorder. [electronic resource] by Lüsebrink, Natalia Porto, Luciana Waterham, Hans R Ferdinandusse, Sacha Rosewich, Hendrik Kurlemann, Gerd Kieslich, Matthias Producer: 20160926 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	131.	Proton NMR spectroscopy of cerebral metabolic alterations in infantile peroxisomal disorders. [electronic resource] by Bruhn, H Kruse, B Korenke, G C Hanefeld, F Hänicke, W Merboldt, K D Frahm, J Producer: 19920702 In: Journal of computer assisted tomography vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	Zellweger syndrome: first reported case in Thailand and literature review. [electronic resource] by Jaruratanasirikul, S Vasiknanont, P Saetung, P Mitarnun, W Producer: 19960626 In: The Southeast Asian journal of tropical medicine and public health vol. 26 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	133.	Contrast enhancement of brainstem tracts in Zellweger spectrum disorder: evidence of inflammatory demyelination? [electronic resource] by Kulkarni, K S Baranano, K W Lin, D D M Raymond, G V Producer: 20110908 In: Neuropediatrics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	134.	Living-donor liver transplantation for mild Zellweger spectrum disorder: Up to 17 years follow-up. [electronic resource] by Demaret, Tanguy Varma, Sharat Stephenne, Xavier Smets, Françoise Scheers, Isabelle Wanders, Ronald Van Maldergem, Lionel Reding, Raymond Sokal, Etienne Producer: 20180919 In: Pediatric transplantation vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	135.	Accurate and live peroxisome biogenesis evaluation achieved by lentiviral expression of a green fluorescent protein fused to a peroxisome targeting signal 1. [electronic resource] by Demaret, Tanguy Courtoy, Guillaume E Ravau, Joachim Van Der Smissen, Patrick Najimi, Mustapha Sokal, Etienne M Producer: 20201214 In: Histochemistry and cell biology vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	[Peroxisomal disorders in neurology]. [electronic resource] by Orii, T Hashimoto, T Producer: 19920528 In: No to hattatsu = Brain and development vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	137.	Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata. [electronic resource] by Schutgens, R B Bouman, I W Nijenhuis, A A Wanders, R J Frumau, M E Producer: 19930923 In: Clinical chemistry vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	138.	Peroxisomal chain-shortening of thromboxane B2: evidence for impaired degradation of thromboxane B2 in Zellweger syndrome. [electronic resource] by Diczfalusy, U Vesterqvist, O Kase, B F Lund, E Alexson, S E Producer: 19931008 In: Journal of lipid research vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	139.	Peroxisomal disorders: genotype, phenotype, major neuropathologic lesions, and pathogenesis. [electronic resource] by Powers, J M Moser, H W Producer: 19980310 In: Brain pathology (Zurich, Switzerland) vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	140.	Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomes. [electronic resource] by Soliman, Kareem Göttfert, Fabian Rosewich, Hendrik Thoms, Sven Gärtner, Jutta Producer: 20191220 In: Scientific reports vol. 8 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.