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	61.	Polarographic studies of saponin-skinned muscle fibres in patients with mitochondrial myopathies. [electronic resource] by Sperl, W Skladal, D Lanznaster, N Schranzhofer, R Zaunschirm, G Gnaiger, E Plöchl, E Gellerich, F Producer: 19950130 In: Journal of inherited metabolic disease vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Hartnup syndrome, progressive encephalopathy and allo-albuminaemia. A clinico-pathological case study. [electronic resource] by Schmidtke, K Endres, W Roscher, A Ibel, H Herschkowitz, N Bachmann, C Plöchl, E Hadorn, H B Producer: 19930204 In: European journal of pediatrics vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Clinical, cytogenetic and molecular analysis of three 46,XX males. [electronic resource] by Plöchl, E Vlasak, I Rittinger, O Bergendi, E Stopar, M Kurnik, P Nachtigall, M Zierler, H Rappold, G A Schiebel, K Producer: 20000621 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Multiorgan donation from a donor with unrecognized ornithine transcarbamylase deficiency. [electronic resource] by Plöchl, W Plöchl, E Pokorny, H Kozek-Langenecker, S Zacherl, J Stöckler-Ipsiroglu, S Wermuth, B Spiss, C K Mühlbacher, F Producer: 20020111 In: Transplant international : official journal of the European Society for Organ Transplantation vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q. [electronic resource] by Mitchell, G A Ozand, P T Robert, M F Ashmarina, L Roberts, J Gibson, K M Wanders, R J Wang, S Chevalier, I Plöchl, E Miziorko, H Producer: 19980406 In: American journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Glutaric aciduria type I: ultrasonographic demonstration of early signs. [electronic resource] by Forstner, R Hoffmann, G F Gassner, I Heideman, P De Klerk, J B Lawrenz-Wolf, B Doringer, E Weiss-Wichert, P Tröger, J Colombo, J P Plöchl, E Producer: 19990330 In: Pediatric radiology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Screening of patients with Turner syndrome for "hidden" Y-mosaicism. [electronic resource] by Vlasak, I Plöchl, E Kronberger, G Bergendi, E Rittinger, O Hagemann, M Schmitt, K Blümel, P Glatzl, J Fekete, G Kadrnka-Lovrencic, M Borkenstein, M Häusler, G Frisch, H Producer: 19990407 In: Klinische Padiatrie vol. 211 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III. [electronic resource] by Lüdecke, H J Schaper, J Meinecke, P Momeni, P Gross, S Hirche, H Abramowicz, M J Albrecht, B Apacik, C Christen, H J Claussen, U Devriendt, K Fastnacht, E Forderer, A Friedrich, U Goodship, T H Greiwe, M Hamm, H Hennekam, R C Hinkel, G K Hoeltzenbein, M Kayserili, H Majewski, F Mathieu, M McLeod, R Midro, A T Moog, U Nagai, T Niikawa, N Orstavik, K H Plöchl, E Seitz, C Schmidtke, J Tranebjaerg, L Tsukahara, M Wittwer, B Zabel, B Gillessen-Kaesbach, G Horsthemke, B Producer: 20010215 In: American journal of human genetics vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)