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	141.	Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata. [electronic resource] by Balfe, A Hoefler, G Chen, W W Watkins, P A Producer: 19900501 In: Pediatric research vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	142.	Polyunsaturated fatty acid changes suggesting a new enzymatic defect in Zellweger syndrome. [electronic resource] by Martinez, M Producer: 19890829 In: Lipids vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	143.	A new peroxisomal beta-oxidation disorder in twin neonates: defective oxidation of both cerotic and pristanic acids. [electronic resource] by Christensen, E Pedersen, S A Leth, H Jakobs, C Schutgens, R B Wanders, R J Producer: 19971106 In: Journal of inherited metabolic disease vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	144.	Molecular basis of Zellweger syndrome, beta-ketothiolase deficiency and mucopolysaccharidoses. [electronic resource] by Orii, T Producer: 19970717 In: The Japanese journal of human genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	145.	Genetic and molecular bases of peroxisome biogenesis disorders. [electronic resource] by Suzuki, Y Shimozawa, N Orii, T Tsukamoto, T Osumi, T Fujiki, Y Kondo, N Producer: 20020131 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	146.	Novel PEX26 Mutation Causing Zellweger Syndrome Presenting as Feeding Intolerance and Hypotonia. [electronic resource] by Stowe, Robert C Agarwal, Sonika Producer: 20190129 In: Pediatric neurology vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	147.	The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor protein. [electronic resource] by Gärtner, J Chen, W W Kelley, R I Mihalik, S J Moser, H W Producer: 19910510 In: Pediatric research vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	148.	Further analysis of the disturbed adrenocortical function in the cerebro-hepato-renal syndrome of Zellweger. [electronic resource] by Govaerts, L Sippell, W G Monnens, L 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)
	149.	Human liver pathology in peroxisomal diseases: a review including novel data. [electronic resource] by Roels, F Espeel, M Poggi, F Mandel, H van Maldergem, L Saudubray, J M Producer: 19930709 In: Biochimie vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	150.	Characterization of human peroxisomal membrane proteins. [electronic resource] by Santos, M J Kawada, M E Espeel, M Figueroa, C Alvarez, A Hidalgo, U Metz, C Producer: 19941104 In: The Journal of biological chemistry vol. 269 Availability: No items available. Save to lists Add to cart (remove)
	151.	Peroxisomal oxidation of the steroid side chain in bile acid formation. [electronic resource] by Pedersen, J I Producer: 19930709 In: Biochimie vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	152.	Preimplantation genetic diagnosis for Zellweger syndrome. [electronic resource] by Al-Sayed, Moeen Al-Hassan, Saad Rashed, Mohamed Qeba, Meshal Coskun, Serdar Producer: 20070914 In: Fertility and sterility vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	153.	Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patients. [electronic resource] by Mihalik, S J Moser, H W Watkins, P A Danks, D M Poulos, A Rhead, W J Producer: 19890612 In: Pediatric research vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	154.	[Zellweger syndrome. Reports on two new cases]. [electronic resource] by Cáceres-Marzal, C Vaquerizo-Madrid, J Girós, M Ruiz, F Roels, F Producer: 20040312 In: Revista de neurologia vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	155.	Fatty acid composition of human myelin proteolipid protein in peroxisomal disorders. [electronic resource] by Bizzozero, O A Zuñiga, G Lees, M B Producer: 19910315 In: Journal of neurochemistry vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	156.	Prenatal diagnosis of Zellweger syndrome using DNA analysis. [electronic resource] by Shimozawa, N Suzuki, Y Orii, T Tsukamoto, T Fujiki, Y Producer: 19930504 In: Prenatal diagnosis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	157.	Zellweger syndrome resulting from maternal isodisomy of chromosome 1. [electronic resource] by Turner, Claire L S Bunyan, David J Thomas, N Simon Mackay, Deborah J G Jones, Huw P Waterham, Hans R Wanders, Ronald J A Temple, I Karen Producer: 20071213 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	158.	Clinical utility gene card for: Zellweger syndrome spectrum. [electronic resource] by Rosewich, Hendrik Waterham, Hans Poll-The, Bwee Tien Ohlenbusch, Andreas Gärtner, Jutta Producer: 20160428 In: European journal of human genetics : EJHG vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	159.	Analysis of very long-chain fatty acids and plasmalogen in the erythrocyte membrane: a simple method for the detection of peroxisomal disorders and discrimination between adrenoleukodystrophy and Zellweger syndrome. [electronic resource] by Tanaka, K Nishizawa, K Yamamoto, H Naruto, T Izeki, E Taga, T Shimada, M Saeki, Y Producer: 19901204 In: Neuropediatrics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	160.	Phenotypic variability (heterogeneity) of peroxisomal disorders. [electronic resource] by Mandel, Hanna Korman, Stanley H 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 604 results.