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	181.	Early events of neocortical assembly: experimental studies and human pathology. [electronic resource] by Caviness, V S Producer: 19891109 In: International journal of neurology vol. 16-17 Availability: No items available. Save to lists Add to cart (remove)
	182.	Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humans. [electronic resource] by Jansen, G A Mihalik, S J Watkins, P A Moser, H W Jakobs, C Denis, S Wanders, R J Producer: 19970109 In: Biochemical and biophysical research communications vol. 229 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	183.	Incidence of peroxisomal disorders in Japan. [electronic resource] by Suzuki, Y Shimozawa, N Yajima, S Inoue, K Orii, T Kondo, N Producer: 19961217 In: The Japanese journal of human genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	184.	Oral bile Acid treatment in two Japanese patients with Zellweger syndrome. [electronic resource] by Maeda, Kohji Kimura, Akihiko Yamato, Yasuhiko Nittono, Hiroshi Takei, Hajime Sato, Tetsuji Mitsubuchi, Hiroshi Murai, Tsuyoshi Kurosawa, Takao Producer: 20021210 In: Journal of pediatric gastroenterology and nutrition vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	185.	Importance of peroxisomes in the formation of chenodeoxycholic acid in human liver. Metabolism of 3 alpha,7 alpha-dihydroxy-5 beta-cholestanoic acid in Zellweger syndrome. [electronic resource] by Kase, B F Pedersen, J I Wathne, K O Gustafsson, J Björkhem, I Producer: 19910410 In: Pediatric research vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	186.	Deficient oxidation of trihydroxycoprostanic acid in liver homogenates from patients with peroxisomal diseases. [electronic resource] by Casteels, M Van Roermund, C W Schepers, L Govaert, L Eyssen, H J Mannaerts, G P Wanders, R J Producer: 19900322 In: Journal of inherited metabolic disease vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	187.	[Clinical, pathological and biochemical abnormality in peroxisomal disorders]. [electronic resource] by Orii, T Suzuki, Y Shimozawa, N Yamaguchi, S Producer: 19900827 In: Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	188.	Fuzzy scaling analysis of a mouse mutant with brain morphological changes. [electronic resource] by Pham, Tuan D Müller, Catharina C Crane, Denis I Producer: 20091005 In: IEEE transactions on information technology in biomedicine : a publication of the IEEE Engineering in Medicine and Biology Society vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	189.	Urinary polyamine and metabolite excretion by children with Zellweger's syndrome. [electronic resource] by Govaerts, L C van den Berg, G A Theeuwes, A Muskiet, F A Monnens, L A Producer: 19910204 In: Clinica chimica acta; international journal of clinical chemistry vol. 192 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	190.	Dihydroxyacetone phosphate acyltransferase and alkyldihydroxyacetone phosphate synthase activities in rat liver subcellular fractions and human skin fibroblasts. [electronic resource] by Singh, H Usher, S Poulos, A Producer: 19890303 In: Archives of biochemistry and biophysics vol. 268 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	191.	Developmental profiles of polyunsaturated fatty acids in the brain of normal infants and patients with peroxisomal diseases: severe deficiency of docosahexaenoic acid in Zellweger's and pseudo-Zellweger's syndromes. [electronic resource] by Martinez, M Producer: 19910725 In: World review of nutrition and dietetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	192.	Metabolism of saturated and polyunsaturated fatty acids by normal and Zellweger syndrome skin fibroblasts. [electronic resource] by Street, J M Johnson, D W Singh, H Poulos, A Producer: 19890908 In: The Biochemical journal vol. 260 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	193.	Plasmalogen content and beta-adrenoceptor signalling in fibroblasts from patients with Zellweger syndrome. Effects of hexadecylglycerol. [electronic resource] by Styger, Regula Wiesmann, Ulrich N Honegger, Ulrich E Producer: 20030108 In: Biochimica et biophysica acta vol. 1585 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	194.	Transformation and characterization of mutant human fibroblasts defective in peroxisome assembly. [electronic resource] by Okamoto, H Suzuki, Y Shimozawa, N Yajima, S Masuno, M Orii, T Producer: 19920903 In: Experimental cell research vol. 201 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	195.	2-Hydroxyphytanic acid oxidase activity in rat and human liver and its deficiency in the Zellweger syndrome. [electronic resource] by Wanders, R J van Roermund, C W Schor, D S ten Brink, H J Jakobs, C Producer: 19950110 In: Biochimica et biophysica acta vol. 1227 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	196.	Recognition of Zellweger syndrome in infancy. [electronic resource] by Grayer, Jennifer Producer: 20050628 In: Advances in neonatal care : official journal of the National Association of Neonatal Nurses vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	197.	Impaired neurogenesis and associated gliosis in mouse brain with PEX13 deficiency. [electronic resource] by Rahim, Rani Sadia St John, James A Crane, Denis I Meedeniya, Adrian C B Producer: 20190131 In: Molecular and cellular neurosciences vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	198.	Peroxisome assembly mutations in humans: structural heterogeneity in Zellweger syndrome. [electronic resource] by Santos, M J Hoefler, S Moser, A B Moser, H W Lazarow, P B Producer: 19920512 In: Journal of cellular physiology vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	199.	Analysis of peroxisomes in lymphoblasts: Zellweger syndrome and a patient with a deletion in chromosome 7. [electronic resource] by Santos, M J Moser, A B Drwinga, H Moser, H W Lazarow, P B Producer: 19930715 In: Pediatric research vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	200.	Cerebrohepatorenal (Zellweger) syndrome: clinical, neuropathological, and biochemical findings. [electronic resource] by Pueschel, S M Oyer, C E Producer: 19960530 In: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery vol. 11 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.