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	1.	Simultaneous determination of cystathionine, total homocysteine, and methionine in dried blood spots by liquid chromatography/tandem mass spectrometry and its utility for the management of patients with homocystinuria. [electronic resource] by Bártl, Josef Chrastina, Petr Krijt, Jakub Hodík, Jakub Pešková, Karolína Kožich, Viktor Producer: 20150512 In: Clinica chimica acta; international journal of clinical chemistry vol. 437 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type I. [electronic resource] by Stiburkova, Blanka Krijt, Jakub Vyletal, Petr Bartl, Josef Gerhatova, Eva Korinek, Martin Sebesta, Ivan Producer: 20120325 In: Clinica chimica acta; international journal of clinical chemistry vol. 413 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Diagnostic tests for primary renal hypouricemia. [electronic resource] by Sebesta, Ivan Stiburkova, Blanka Bartl, Josef Ichida, Kimiyoshi Hosoyamada, Makoto Taylor, Judy Marinaki, Anthony Producer: 20120321 In: Nucleosides, nucleotides & nucleic acids vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Modern diagnostic approach to hereditary xanthinuria. [electronic resource] by Mraz, Martin Hurba, Olha Bartl, Josef Dolezel, Zdenek Marinaki, Anthony Fairbanks, Lynette Stiburkova, Blanka Producer: 20160204 In: Urolithiasis vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Newborn screening for homocystinurias: Recent recommendations versus current practice. [electronic resource] by Keller, Rebecca Chrastina, Petr Pavlíková, Markéta Gouveia, Sofía Ribes, Antonia Kölker, Stefan Blom, Henk J Baumgartner, Matthias R Bártl, Josef Dionisi-Vici, Carlo Gleich, Florian Morris, Andrew A Kožich, Viktor Huemer, Martina Barić, Ivo Ben-Omran, Tawfeq Blasco-Alonso, Javier Bueno Delgado, Maria A Carducci, Claudia Cassanello, Michela Cerone, Roberto Couce, Maria Luz Crushell, Ellen Delgado Pecellin, Carmen Dulin, Elena Espada, Mercedes Ferino, Giulio Fingerhut, Ralph Garcia Jimenez, Immaculada Gonzalez Gallego, Immaculada González-Irazabal, Yolanda Gramer, Gwendolyn Juan Fita, Maria Jesus Karg, Eszter Klein, Jeanette Konstantopoulou, Vassiliki la Marca, Giancarlo Leão Teles, Elisa Leuzzi, Vincenzo Lilliu, Franco Lopez, Rosa Maria Lund, Allan M Mayne, Philip Meavilla, Silvia Moat, Stuart J Okun, Jürgen G Pasquini, Elisabeta Pedron-Giner, Consuélo Carmen Racz, Gabor Zoltan Ruiz Gomez, Maria Angeles Vilarinho, Laura Yahyaoui, Raquel Zerjav Tansek, Moja Zetterström, Rolf H Zeyda, Maximilian Producer: 20200401 In: Journal of inherited metabolic disease vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)