Fibroblast Growth Factor 23 and Matrix-Metalloproteinases in Patients with Chronic Kidney Disease: Are They Associated with Cardiovascular Disease? von Peiskerová, M., Kalousová, M., Kratochvílová, M., Dusilová-Sulková, S., Uhrová, J., Bandúr, S., Malbohan, I.M., Zima, T., Tesař, V.

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Lipoprotein lipase deficiency: clinical, biochemical and molecular characteristics in three patients with novel mutations in the LPL gene von Kolářová, H, Tesařová, M, Švecová, Š, Stránecký, V, Přistoupilová, A, Zima, T, Uhrová, J, Volgina, S Y, Zeman, J, Honzík, T

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Genetic variants in haem oxygenase-1 and endothelial nitric oxide synthase influence the extent and evolution of coronary artery atherosclerosis von Král, A, Kovárník, T, Králík, L, Skalická, H, Horák, J, Mintz, G S, Uhrová, J, Sonka, M, Wahle, A, Downe, R, Aschermann, M, Martásek, P, Linhart, A

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Advanced glycoxidation end products in patients with multiple sclerosis von Kalousová, M, Havrdová, E, Mrázová, K, Spacek, P, Braun, M, Uhrová, J, Germanová, A, Zima, T

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Comparison of Different Immunoassays for CA 19-9 von Stern, Petr, Friedecky, Bedrich, Bartos, Vladimir, Bezdickova, Drahomira, Vavrova, Jaroslava, Uhrova, Jana, Rozprimova, Ladislava, Zima, Tomas, Palicka, Vladimir

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Dissociative symptoms reflect levels of tumor necrosis factor alpha in patients with unipolar depression von Bizik, Gustav, Bob, Petr, Raboch, Jiri, Pavlat, Josef, Uhrova, Jana, Benakova, Hana, Zima, Tomas

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Elevation of procalcitonin in chronic dialysed patients von Brodska, H, Malickova, K, Kazda, A, Lachmanova, J, Uhrova, J, Zima, T

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Myelin basic protein in multiple sclerosis and other neurological disorders von Kalistová, Hana, Havrdová, Eva, Uhrová, Jana, Zeman, David, Týblová, Michaela, Mrázová, Katerina

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Comparability of Eight Immunoassay Procedures for the Determination of CA 15-3 and Related Markers von Stern, Petr, Bartos, Vladimir, Vavrova, Jaroslava, Bezdickova, Drahomira, Pechova, Martina, Uhrova, Jana, Friedecky, Bedrich, Sprongl, Ludek, Zima, Tomas, Palicka, Vladimir

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Species limits and phylogeographic structure in two genera of solitary African mole-rats Georychus and Heliophobius von Uhrová, M., Mikula, O., Bennett, N.C, Van Daele, P., Piálek, L., Bryja, J., Visser, J.H., Jansen van Vuuren, B., Šumbera, R.

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The comparability of different neuron-specific enolase immunoassays and its impact on external quality assessment system von Štern, Petr, Bartoš, V, Uhrová, J, Springer, Drahomíra, Vaníčková, Z, Tichý, V, Průša, Richard, Zima, Tomáš

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Late Ordovician magmatic pulse in the Tugrug Group, the Gobi Altai Zone, SW Mongolia von Hanžl, P., Uhrová, L., Hrdličková, K., Schulmann, K., Buriánek, D., Gansukh, O., Míková, J.

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PP-26 Serum enzyme activities in monitoring melim melanoma progression and regression von Borovansky, J., Horak, V., Uhrova, J., Zima, T., Elleder, M.

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The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients von Metzger, Silke, Walter, Carolin, Riess, Olaf, Roos, Raymund A C, Nielsen, Jørgen E, Craufurd, David, Nguyen, Huu Phuc

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An annotated list and molecular data on larvae of gryporhynchid tapeworms (Cestoda: Cyclophyllidea) from freshwater fishes in Africa von Scholz, Tomáš, Tavakol, Sareh, Uhrová, Lucie, Brabec, Jan, Přikrylová, Iva, Mašová, Šárka, Šimková, Andrea, Halajian, Ali, Luus-Powell, Wilmien J.

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Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia von Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Muller, Juliane S., Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie, Santorelli, Filippo M., Alfares, Ahmed A., Zhu, Changlian, Meszarosova, Anna Uhrova, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R., Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T., Strom, Tim M., De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana, Alfadhel, Majid, van de Warrenburg, Bart P., Portier, Ruben, Bergmann, Carsten, Firouzabadi, Saghar Ghasemi, Jin, Sheng Chih, Bilguvar, Kaya, Hamed, Sherifa, Abdelhameed, Mohammed, Haridy, Nourelhoda A., Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair, Wood, Nick W., Mau-Them, Frederic Tran, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele, Zara, Federico, Salpietro, Vincenzo, Scala, Marcello, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laetitia, Schmitt, Emmanuelle, Lacaze, Elodie, Kuepper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J. H., Grand, Katheryn, Graham, John M., Lewis, Richard A., Millan, Francisca, Duman, Ozgur, Dundar, Nihal, Uyanik, Gokhan, Schols, Ludger, Nuernberg, Peter, Nuernberg, Gudrun, Bordes, Andrea Catala, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Boucanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S., Shamseldin, Hanan, Al Tala, Saeed, Varaghchi, Jamileh Rezazadeh, Najafi, Maryam, Deschner, Selina, Glaeser, Dieter, Huettel, Wolfgang, Kruer, Michael C., Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Zuchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schuele, Rebecca, Horvath, Rita

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Preparation, characterization and cytotoxicity of schizophyllan/silver nanoparticle composite von Abdel-Mohsen, A.M., Abdel-Rahman, Rasha M., Fouda, Moustafa M.G., Vojtova, L., Uhrova, L., Hassan, A.F., Al-Deyab, Salem S., El-Shamy, Ibrahim E., Jancar, J.

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Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study von Moss, Davina J Hensman, MBBS, Pardiñas, Antonio F, PhD, Langbehn, Douglas, Prof, Lo, Kitty, PhD, Leavitt, Blair R, Prof, Roos, Raymund, Prof, Durr, Alexandra, Prof, Mead, Simon, Prof, Holmans, Peter, Prof, Jones, Lesley, Prof, Tabrizi, Sarah J, Prof

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Clinical and genetic features of five Czech patients with SPG11 von Doleckova, K., Uhrova, A. Meszarosova, Stellmachová, J., Gescheidt, T., Sigut, V., Houska, P., Seeman, P., Roth, J.

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Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutations von Nagy, Sara, Pagnamenta, Alistair T, Cali, Elisa, Braakman, Hilde M H, Wijntjes, Juerd, Kusters, Benno, Gotkine, Marc, Elpeleg, Orly, Meiner, Vardiella, Lenberg, Jerica, Wigby, Kristen, Friedman, Jennifer, Perry, Luke D, Rossor, Alexander M, Uhrova Meszarosova, Anna, Thomasova, Dana, Jacob, Saiju, O'Driscoll, Mary, De Simone, Lenika, Grange, Dorothy K, Sommerville, Richard, Firoozfar, Zahra, Alavi, Shahryar, Mazaheri, Mahta, Parmar, Jevin M, Lamont, Phillipa J, Pini, Veronica, Sarkozy, Anna, Muntoni, Francesco, Ravenscroft, Gianina, Jones, Eppie, O'Rourke, Declan, Nel, Melissa, Heckmann, Jeannine M, Kvalsund, Michelle, Kapapa, Musambo M, Wa Somwe, Somwe, Bearden, David R, Çakar, Arman, Childs, Anne-Marie, Horvath, Rita, Reilly, Mary M, Houlden, Henry, Maroofian, Reza

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