Assessment of the contamination of riparian soil and vegetation by trace metals — A Danube River case study
Pavlović, P., Mitrović, M., Đorđević, D., Sakan, S., Slobodnik, J., Liška, I., Csanyi, B., Jarić, S., Kostić, O., Pavlović, D., Marinković, N., Tubić, B., Paunović, M.
Published in The Science of the total environment (01.01.2016)
Published in The Science of the total environment (01.01.2016)
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Application of an electrified benthic frame trawl for sampling fish in a very large European river (the Danube River) – Is offshore monitoring necessary?
Szalóky, Z., György, Á.I., Tóth, B., Sevcsik, A., Specziár, A., Csányi, B., Szekeres, J., Erős, T.
Published in Fisheries research (01.03.2014)
Published in Fisheries research (01.03.2014)
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Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene
Ebberink, Merel S, Csanyi, Barbara, Chong, Wui K, Denis, Simone, Sharp, Peter, Mooijer, Petra A W, Dekker, Conny J M, Spooner, Claire, Ngu, Lock H, De Sousa, Carlos, Wanders, Ronald J A, Fietz, Michael J, Clayton, Peter T, Waterham, Hans R, Ferdinandusse, Sacha
Published in Journal of medical genetics (01.09.2010)
Published in Journal of medical genetics (01.09.2010)
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Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNA(Lys) associated with dystonia and stroke-like episodes
Gal, A, Pentelenyi, K, Remenyi, V, Pal, Z, Csanyi, B, Tomory, G, Rasko, I, Molnar, M J
Published in Acta neurologica Scandinavica (01.10.2010)
Published in Acta neurologica Scandinavica (01.10.2010)
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Journal Article
Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNALys associated with dystonia and stroke-like episodes
Gal, A., Pentelenyi, K., Remenyi, V., Pal, Z., Csanyi, B., Tomory, G., Rasko, I., Molnar, M. J.
Published in Acta neurologica Scandinavica (01.10.2010)
Published in Acta neurologica Scandinavica (01.10.2010)
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Y‐Chromosome Analysis of Ancient Hungarian and Two Modern Hungarian‐Speaking Populations from the Carpathian Basin
Csányi, B., Bogácsi‐Szabó, E., Tömöry, Gy, Czibula, Á., Priskin, K., Csõsz, A., Mende, B., Langó, P., Csete, K., Zsolnai, A., Conant, E. K., Downes, C. S., Raskó, I.
Published in Annals of human genetics (01.07.2008)
Published in Annals of human genetics (01.07.2008)
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Mitochondrial sequence variation in ancient horses from the Carpathian Basin and possible modern relatives
Priskin, K, Szabó, K, Tömöry, G, Bogácsi-Szabó, E, Csányi, B, Eördögh, R, Downes, C. S, Raskó, I
Published in Genetica (01.02.2010)
Published in Genetica (01.02.2010)
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Consensus clinical management guideline for pantothenate kinase-associated neurodegeneration (PKAN)
Hogarth, Penelope, Kurian, Manju A., Gregory, Allison, Csányi, Barbara, Zagustin, Tamara, Kmiec, Tomasz, Wood, Patricia, Klucken, Angelika, Scalise, Natale, Sofia, Francesca, Klopstock, Thomas, Zorzi, Giovanna, Nardocci, Nardo, Hayflick, Susan J.
Published in Molecular genetics and metabolism (01.03.2017)
Published in Molecular genetics and metabolism (01.03.2017)
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Conference Proceeding
Approaches for sediment associated pollutant monitoring in the River Danube
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Conference Proceeding
P259 – 2083 Whole exome sequencing study aids diagnosis of atypical pantothenate kinase associated neurodegeneration (PKAN)
Csanyi, B, Kaminska, M, Meyer, E, Josifova, D, Siddiqui, A, Lumsden, D, Kara, E, Houlden, H, Hardy, J, Révész, T, Kurian, MA, Lin, JP
Published in European journal of paediatric neurology (01.09.2013)
Published in European journal of paediatric neurology (01.09.2013)
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Journal Article
Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNALys associated with dystonia and stroke-like episodes: New mitochondrial tRNALys mutation with dystonia
Gal, A., Pentelenyi, K., Remenyi, V., Pal, Z., Csanyi, B., Tomory, G., Rasko, I., Molnar, M. J.
Published in Acta neurologica Scandinavica (01.10.2010)
Published in Acta neurologica Scandinavica (01.10.2010)
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P273 – 1998 TH-negative infantile-onset severe dopamine deficiency syndrome
Ng, J, Tuschl, K, Csanyi, B, Kinali, M, Devlin, A, Carr, LJ, Cleary, M, Manzur, AY, Gissen, P, Garcia Cazorla, A, Artuch, R, Clayton, PT, Heales, SJR, Kurian, MA
Published in European journal of paediatric neurology (01.09.2013)
Published in European journal of paediatric neurology (01.09.2013)
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Natural History of Vanishing White Matter
Hamilton, Eline M. C., van der Lei, Hannemieke D. W., Lourenço, Charles M., Naidu, Sakkubai, Mierzewska, Hanna, de Vet, Henrica C. W., Uitdehaag, Bernard M. J., Lissenberg‐Witte, Birgit I., Aldhalaan, H., Alves, D., Appleton, R., Arslan, E.A., Baethmann, M., Banwell, B., Barbot, C., Bertini, E., Bley, A., Bollen, L., Boltshauser, E., Bower, S., Bravo Oro, A., Campos, M.M., Carr, L., Chan, A.K.J., Clarke, A., Crow, Y., Csányi, B., Del Rossario Aldao, M., D'Hooghe, M., El Helou, J, Fallon, P., Ferlini, A., Ferro, J.M., Fluss, J., Fontenelle, L., Garone, C., Geldhoff, M., Glamuzina, E., Góes, F., Gonzalez, V., Guarda, C., Gulati, S., Güler, S., Horvath, R., Jagadeesh, S., Kaczorowska, M., Kankirawatana, P., Karall, D., King, M.D., Krägeloh‐Mann, I., Lehman, A., Liptai, Z., Livingston, J.H., Maes, M., Majumdar, A., Mandel, H., McEntagart, M., Morton, R., Moura de Souza, C.F., Mundy, H., Naess, K., Naismith, K., Newton, R.W., Noetzel, M.J., O'Brien, B, Okálová, K., Østergaard, J.R., Pato Pato, A., Pera, J., Perlman, S., Philippart, M., Régal, L., Rice, C.M., Rossignol, E., Rubin, J.P., Salvi, F., Sampaio, H., Sánchez Herrero, J., Santos, E., Sessa, M., Sharma, S., Shearn, J., Shoffner, J., Skranes, J.S., Sparagana, S.P., Storey, E., Sztriha, L., Tatli, B., Tekturk, P., Tennison, M., Tirupathi, S., Toledo Bravo de Laguna, L., Tuna, M.A., Valverde, A., van Coster, R., Vasconcelos, M., Vogt, H., von Kleist‐Retzow, J.C., Wong, S.S.N., Yavuz, H.
Published in Annals of neurology (01.08.2018)
Published in Annals of neurology (01.08.2018)
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Genetic and clinical diagnosis of Angelman syndrome. Case Reviews
García Ramírez, M, Csanyi, B, Martínez Antón, J, Delgado Marqués, M, Bauzano Poley, E
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.09.2008)
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Published in Anales de pediatría (Barcelona, Spain : 2003) (01.09.2008)
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Mitochondrial DNA of Ancient Cumanians: Culturally Asian Steppe Nomadic Immigrants with Substantially More Western Eurasian Mitochondrial DNA Lineages
BOGÁCSI-SZABÓ, ERIKA, KALMÁR, TIBOR, CSÁNYI, BERNADETT, TÖMÖRY, GYÖNGYVÉR, CZIBULA, ÁGNES, PRISKIN, KATALIN, HORVÁTH, FERENC, DOWNES, CHRISTOPHER STEPHEN, RASKÓ, ISTVÁN
Published in Human biology (01.10.2005)
Published in Human biology (01.10.2005)
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