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	1.	Coexistence of deficiencies of uroporphyrinogen III synthase and decarboxylase in a patient with congenital erythropoietic porphyria and in his family. [electronic resource] by Freesemann, A G Hofweber, K Doss, M O Producer: 19970519 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)
	2.	Interdependence between degree of porphyrin excess and disease severity in congenital erythropoietic porphyria (Günther's disease). [electronic resource] by Freesemann, A G Bhutani, L K Jacob, K Doss, M O Producer: 19970731 In: Archives of dermatological research vol. 289 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Immunological, enzymatic and biochemical studies of uroporphyrinogen III-synthase deficiency in 20 patients with congenital erythropoietic porphyria. [electronic resource] by Freesemann, A G Gross, U Bensidhoum, M de Verneuil, H Doss, M O Producer: 19981110 In: European journal of biochemistry vol. 257 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Compound heterozygous hereditary coproporphyria with fluorescing teeth. [electronic resource] by Doss, M O Gross, U Lamoril, J Kranl, C Jacob, K Doss, M da Silva, V Freesemann, A G Deybach, J C Sepp, N Nordmann, Y Producer: 19991018 In: Annals of clinical biochemistry vol. 36 ( Pt 5) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)