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	241.	A case of pseudo-Zellweger syndrome with a possible bifunctional enzyme deficiency but detectable enzyme protein. Comparison of two cases of Zellweger syndrome. [electronic resource] by Nakada, Y Hyakuna, N Suzuki, Y Shimozawa, N Takaesu, E Ikema, R Hirayama, K Producer: 19940505 In: Brain & development vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	242.	Studies on the urinary excretion of thromboxane B2 in Zellweger patients and control subjects: evidence for a major role for peroxisomes in the beta-oxidative chain-shortening of thromboxane B2. [electronic resource] by de Waart, D R Koomen, G C Wanders, R J Producer: 19940513 In: Biochimica et biophysica acta vol. 1226 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	243.	Stereochemistry of pipecolic acid found in the urine and plasma of subjects with peroxisomal deficiencies. [electronic resource] by Armstrong, D W Zukowski, J Ercal, N Gasper, M Producer: 19940311 In: Journal of pharmaceutical and biomedical analysis vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	244.	Zellweger syndrome with unusual findings: non-immune hydrops fetalis, dermal erythropoiesis and hypoplastic toe nails. [electronic resource] by Dursun, Ali Gucer, Safak Ebberink, M S Yigit, Sule Wanders, R J A Waterham, H R Producer: 20130805 In: Journal of inherited metabolic disease vol. 32 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	245.	Biochemical and genetic characterization of an unusual mild PEX3-related Zellweger spectrum disorder. [electronic resource] by Bjørgo, Kathrine Fjær, Roar Mørk, Hanne Håberg Ferdinandusse, Sacha Falkenberg, Kim D Waterham, Hans R Øye, Ane-Marte Sikiric, Alma Amundsen, Silja Svanstrøm Kulseth, Mari Ann Selmer, Kaja Producer: 20180403 In: Molecular genetics and metabolism vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	246.	Prenatal diagnosis of Zellweger syndrome by direct visualization of peroxisomes in chorionic villus fibroblasts by immunofluorescence microscopy. [electronic resource] by Wanders, R J Wiemer, E A Brul, S Schutgens, R B van den Bosch, H Tager, J M Producer: 19900125 In: Journal of inherited metabolic disease vol. 12 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	247.	Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group. [electronic resource] by Poulos, A Christodoulou, J Chow, C W Goldblatt, J Paton, B C Orii, T Suzuki, Y Shimozawa, N Producer: 19951120 In: The Journal of pediatrics vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	248.	Protein import deficiencies in human peroxisomal disorders. [electronic resource] by Wiemer, E A Subramani, S Producer: 19950103 In: Molecular genetic medicine vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	249.	Topology of catalase assembly in human skin fibroblasts. [electronic resource] by Middelkoop, E Wiemer, E A Schoenmaker, D E Strijland, A Tager, J M Producer: 19940128 In: Biochimica et biophysica acta vol. 1220 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	250.	Postmortem findings and prenatal diagnosis of Zellweger syndrome. Case report. [electronic resource] by Lindhard, A Graem, N Skovby, F Jeppesen, D Producer: 19930709 In: APMIS : acta pathologica, microbiologica, et immunologica Scandinavica vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	251.	A new autosomal recessive syndrome with Zellweger-like manifestations. [electronic resource] by Ahn, Joe K Lev, Dorit Leshinsky-Silver, Esther Ginzberg, Mira Lerman-Sagie, Tally Producer: 20040203 In: American journal of medical genetics. Part A vol. 119A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	252.	Poor vision, deafness, hypotonia . . . with pupillary membranes. [electronic resource] by Berman, Jeffrey L Producer: 20130717 In: Journal of pediatric ophthalmology and strabismus vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	253.	Late-onset Zellweger spectrum disorder caused by PEX6 mutations mimicking X-linked adrenoleukodystrophy. [electronic resource] by Tran, Christel Hewson, Stacy Steinberg, Steven J Mercimek-Mahmutoglu, Saadet Producer: 20151021 In: Pediatric neurology vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	254.	Atypical PEX16 peroxisome biogenesis disorder with mild biochemical disruptions and long survival. [electronic resource] by Zaabi, Nuha Al Kendi, Anoud Al-Jasmi, Fatma Takashima, Shigeo Shimozawa, Nobuyuki Al-Dirbashi, Osama Y Producer: 20190325 In: Brain & development vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	255.	Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype. [electronic resource] by Gärtner, J Preuss, N Brosius, U Biermanns, M 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)
	256.	Elevated urinary excretion of nitric oxide metabolites in young infants with Zellweger syndrome. [electronic resource] by Surdacki, Andrzej Tsikas, Dimitrios Mayatepek, Ertan Frölich, Jürgen C Producer: 20031223 In: Clinica chimica acta; international journal of clinical chemistry vol. 334 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	257.	[Subependymal pseudocysts in the fetal brain revealing Zellweger syndrome]. [electronic resource] by Cuillier, F Cartault, F Lemaire, P Gruau, M Alessandri, J-L Producer: 20040805 In: Journal de gynecologie, obstetrique et biologie de la reproduction vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	258.	Cholesterol biosynthesis in Zellweger syndrome: normal activity of mevalonate kinase, mevalonate-5'-pyrophosphate decarboxylase and IPP-isomerase in patients' fibroblasts but deficient mevalonate kinase activity in liver. [electronic resource] by Wanders, R J Romeijn, G J Producer: 19961004 In: Journal of inherited metabolic disease vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	259.	Sphinganine 1-phosphate metabolism in cultured skin fibroblasts: evidence for the existence of a sphingosine phosphatase. [electronic resource] by Van Veldhoven, P P Mannaerts, G P Producer: 19940617 In: The Biochemical journal vol. 299 ( Pt 3) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	260.	Formation and release of a peroxisome-dependent arachidonic acid metabolite by human skin fibroblasts. [electronic resource] by Gordon, J A Heller, S K Kaduce, T L Spector, A A Producer: 19940317 In: The Journal of biological chemistry vol. 269 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 604 results.