N25 Are sextant biopsies still justified? von Milonas, D, Zabarskas, A, Masilunas, J, Kucinskas, K, Auskalnis, S, Jievaltas, M

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NSD1 duplication in Silver–Russell syndrome (SRS): molecular karyotyping in patients with SRS features von Sachwitz, J., Meyer, R., Fekete, G., Spranger, S., Matulevičienė, A., Kučinskas, V., Bach, A., Luczay, A., Brüchle, N.O., Eggermann, K., Zerres, K., Elbracht, M., Eggermann, T.

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Mutation History of the Roma/Gypsies von Morar, Bharti, Gresham, David, Angelicheva, Dora, Tournev, Ivailo, Gooding, Rebecca, Guergueltcheva, Velina, Schmidt, Carolin, Abicht, Angela, Lochmüller, Hanns, Tordai, Attila, Kalmár, Lajos, Nagy, Melinda, Karcagi, Veronika, Jeanpierre, Marc, Herczegfalvi, Agnes, Beeson, David, Venkataraman, Viswanathan, Warwick Carter, Kim, Reeve, Jeff, de Pablo, Rosario, Kučinskas, Vaidutis, Kalaydjieva, Luba

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Comparison of the Efficacy and Safety of Live Attenuated Cold-Adapted Influenza Vaccine, Trivalent, With Trivalent Inactivated Influenza Virus Vaccine in Children and Adolescents W... von Fleming, Douglas M, Crovari, Pietro, Wahn, Ulrich, Klemola, Timo, Schlesinger, Yechiel, Langussis, Alexangros, Øymar, Knut, Garcia, Maria Luz, Krygier, Alain, Costa, Herculano, Heininger, Ulrich, Pregaldien, Jean-Louis, Cheng, Sheau-Mei, Skinner, Jonathan, Razmpour, Ahmad, Saville, Melanie, Gruber, William C, Forrest, Bruce

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The design and performance of the Gaia photometric system von Jordi, C., Høg, E., Brown, A. G. A., Lindegren, L., Bailer-Jones, C. A. L., Carrasco, J. M., Knude, J., Straižys, V., De Bruijne, J. H. J., Claeskens, J.-F., Drimmel, R., Figueras, F., Grenon, M., Kolka, I., Perryman, M. A. C., Tautvaišiene, G., Vansevičius, V., Willemsen, P. G., Bridžius, A., Evans, D. W., Fabricius, C., Fiorucci, M., Heiter, U., Kaempf, T. A., Kazlauskas, A., Kučinskas, A., Malyuto, V., Munari, U., Reylé, C., Torra, J., Vallenari, A., Zdanavičius, K., Korakitis, R., Malkov, O., Smette, A.

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A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features von Preiksaitiene, E, Männik, K, Dirse, V, Utkus, A, Ciuladaite, Z, Kasnauskiene, J, Kurg, A, Kučinskas, V

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First reported case of lysinuric protein intolerance (LPI) in Lithuania, confirmed biochemically and by DNA analysis von Cimbalistiene, Loreta, Lehnert, Willy, Huoponen, Kirsi, Kucinskas, Vaidutis

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Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction von den Hoed, Joery, de Boer, Elke, Voisin, Norine, Dingemans, Alexander J.M., Guex, Nicolas, Wiel, Laurens, Nellaker, Christoffer, Amudhavalli, Shivarajan M., Banka, Siddharth, Bena, Frederique S., Ben-Zeev, Bruria, Bonagura, Vincent R., Bruel, Ange-Line, Brunet, Theresa, Brunner, Han G., Chew, Hui B., Chrast, Jacqueline, Cimbalistienė, Loreta, Coon, Hilary, Délot, Emmanuèlle C., Démurger, Florence, Denommé-Pichon, Anne-Sophie, Depienne, Christel, Donnai, Dian, Dyment, David A., Elpeleg, Orly, Faivre, Laurence, Gilissen, Christian, Granger, Leslie, Haber, Benjamin, Hachiya, Yasuo, Abedi, Yasmin Hamzavi, Hanebeck, Jennifer, Hehir-Kwa, Jayne Y., Horist, Brooke, Itai, Toshiyuki, Jackson, Adam, Jewell, Rosalyn, Jones, Kelly L., Joss, Shelagh, Kashii, Hirofumi, Kato, Mitsuhiro, Kattentidt-Mouravieva, Anja A., Kok, Fernando, Kotzaeridou, Urania, Krishnamurthy, Vidya, Kučinskas, Vaidutis, Kuechler, Alma, Lavillaureix, Alinoë, Liu, Pengfei, Manwaring, Linda, Matsumoto, Naomichi, Mazel, Benoît, McWalter, Kirsty, Meiner, Vardiella, Mikati, Mohamad A., Miyatake, Satoko, Mizuguchi, Takeshi, Moey, Lip H., Mohammed, Shehla, Mor-Shaked, Hagar, Mountford, Hayley, Newbury-Ecob, Ruth, Odent, Sylvie, Orec, Laura, Osmond, Matthew, Palculict, Timothy B., Parker, Michael, Petersen, Andrea K., Pfundt, Rolph, Preikšaitienė, Eglė, Radtke, Kelly, Ranza, Emmanuelle, Rosenfeld, Jill A., Santiago-Sim, Teresa, Schwager, Caitlin, Sinnema, Margje, Snijders Blok, Lot, Spillmann, Rebecca C., Stegmann, Alexander P.A., Thiffault, Isabelle, Tran, Linh, Vaknin-Dembinsky, Adi, Vedovato-dos-Santos, Juliana H., Schrier Vergano, Samantha A., Vilain, Eric, Vitobello, Antonio, Wagner, Matias, Waheeb, Androu, Willing, Marcia, Zuccarelli, Britton, Kini, Usha, Newbury, Dianne F., Kleefstra, Tjitske, Reymond, Alexandre, Fisher, Simon E., Vissers, Lisenka E.L.M.

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Athlome Project Consortium: a concerted effort to discover genomic and other "omic" markers of athletic performance von Pitsiladis, Yannis P, Tanaka, Masashi, Eynon, Nir, Bouchard, Claude, North, Kathryn N, Williams, Alun G, Collins, Malcolm, Moran, Colin N, Britton, Steven L, Fuku, Noriyuki, Ashley, Euan A, Klissouras, Vassilis, Lucia, Alejandro, Ahmetov, Ildus I, de Geus, Eco, Alsayrafi, Mohammed

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Rheumatoid arthritis in Poland and Lithuania: different clinical course and HLA associations despite similar genetic background von Płoski, R, Butrimiene, I, Kamińska, E, Valiukiene, K, Sliwińska, P, Kubasiewicz, E, Kozakiewicz, A, Smerdel, A, Kučinskas, V, Jaworski, J, Jastrzębska, E, Forre, O, Venalis, A, Pazdur, J

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Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States von Kurzawski, G, Suchy, J, Kładny, J, Safranow, K, Jakubowska, A, Elsakov, P, Kucinskas, V, Gardovski, J, Irmejs, A, Sibul, H, Huzarski, T, Byrski, T, Dębniak, T, Cybulski, C, Gronwald, J, Oszurek, O, Clark, J, Góźdź, S, Niepsuj, S, Słomski, R, Pławski, A, Łącka-Wojciechowska, A, Rozmiarek, A, Fiszer-Maliszewska, Ł, Bębenek, M, Sorokin, D, Stawicka, M, Godlewski, D, Richter, P, Brożek, I, Wysocka, B, Jawień, A, Banaszkiewicz, Z, Kowalczyk, J, Czudowska, D, Goretzki, P E, Moeslein, G, Lubiński, J

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Can we trust elemental abundances derived in late-type giants with the classical 1D stellar atmosphere models? von Kučinskas, A., Dobrovolskas, V., Ivanauskas, A., Ludwig, H.-G., Caffau, E., Blaževičius, K., Klevas, J., Prakapavičius, D.

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Analysis of shared heritability in common disorders of the brain von Anttila, Verneri, Bras, Jose, Duncan, Laramie, Wei, Zhi, Grenier-Boley, Benjamin, Berr, Claudine, Letenneur, Luc, Boland, Anne, Duron, Emmanuelle, Huentelman, Matthew J, St George-Hyslop, Peter, Head, Elizabeth, Levey, Allan I, Lieberman, Andrew P, Lawlor, Brian, Boada, Mercè, Rice, Kenneth, De Jager, Philip L, Rotter, Jerome I, Alegret, Montserrat, Winsvold, Bendik, Gordon, Scott D, Adams, Hieab H.H, Artto, Ville, Kaunisto, Mari, Montgomery, Grant W, Muller-Myhsok, Bertram, Kaprio, Jaakko, Kubisch, Christian, Berkovic, Samuel, Bradfield, Jonathan, Buono, Russell, French, Jacqueline, Kunz, Wolfram S, Leu, Costin, Møller, Rikke S, Striano, Pasquale, Visscher, Frank, Zara, Federico, Heinzen, Erin L, Marson, Anthony, Morris, Huw R, Bevan, Steve, Rothwell, Peter, Pera, Joana, Boraska Perica, Vesna, Rybakowski, Filip, Keski-Rahkonen, Anna, Hudson, James I, van Elburg, Annemarie A, Hauser, Joanna, Tziouvas, Konstantinos, Papezova, Hana, Schosser, Alexandra, Szatkiewicz, Jin Peng, Rothenberger, Aribert, Banaschewski, Tobias, Freitag, Christine, Loo, Sandra K, Bailey, Anthony, Battaglia, Agatino, Celestino-Soper, Patrícia, Matthews, Keith, Morris, Derek, Jamain, Stéphane, Maaser, Anna, Reinbold, Céline S, Schumacher, Johannes, Rice, John, Craddock, Nick, Rouleau, Guy A, Ophoff, Roel, Pato, Carlos, Posthuma, Danielle, Air, Tracy, Nauck, Matthias, Schoevers, Robert A, Darrow, Sabrina, Denys, Damiaan, Fernandez, Thomas, Greenberg, Erica, Hoekstra, Pieter J, Huang, Alden, Illmann, Cornelia, Leventhal, Bennett, Miguel, Eurípedes C, Nicolini, Humberto, Stein, Dan J, Van Nieuwerburgh, Filip, Weatherall, Sarah, Crespo-Facorro, Benedicto, Lee Chee Keong, Jimmy, Mattheisen, Manuel, Quested, Digby, Gejman, Pablo V, Mattingsdal, Morten, Oh, Sang-Yun, Scott, Rodney, Faraone, Stephen V, Mathews, Carol A

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Use of broad-spectrum antibiotics in children diagnosed with multisystem inflammatory syndrome temporarily associated with SARS-CoV-2 infection in Poland: the MOIS-CoR study von Toczyłowski, Kacper, Łasecka-Zadrożna, Joanna, Pałyga-Bysiecka, Ilona, Ludwikowska, Kamila Maria, Okarska-Napierała, Magdalena, Dudek, Natalia, Afelt, Aneta, Suski, Catherine, Kursa, Miron Bartosz, Jackowska, Teresa, Kuchar, Ernest, Szenborn, Leszek, Sawicka, Marta, BerdejSzczot, Elżbieta, Brzuszkiewicz, Sebastian, Buda, Piotr, Czajka, Alicja, Czech, Agnieszka, Czerwińska, Ewa, Figlerowicz, Magdalena, FirekPędras, Małgorzata, Gawlik, Aneta, Gowin, Ewelina, Izdebska, Olga, JanuszkiewiczLewandowska, Danuta, Kiepuszka, Justyna, Koczwara, Agnieszka, Koszałko, Danuta, KośmiderŻurawska, Magdalena, Książyk, Janusz, Kucińska, Beata, Kukawska, Martyna, Lackowska, Anita, Łapacz, Katarzyna, Maliszak, Agnieszka, Mania, Anna, Mańdziuk, Joanna, Mazur, Artur, Niszczota, Cezary, OpalińskaZielonka, Paulina, Rojewska, Katarzyna, RożnowskaWójtowicz, Anna, Siewert, Bartosz, Sobiczewska, Paulina, Stopyra, Lidia, StrobaŻelek, Agnieszka, StryczyńskaKazubska, Joanna, Sulik, Artur, Szatkowski, Tomasz, Szczepańska, Barbara, Szczukocki, Maciej, Szylo, Robert, Tyc, Filip, Wielgos, Katarzyna, Wołowska, Ewa, Wysocki, Jacek, Zacharzewska, Anna, Zaniew, Marcin, Zielińska, Marzena, ZiębaGlonek, Katarzyna, Mazur-Melewska, Katarzyna

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The LWb Blood Group as a Marker of Prehistoric Baltic Migrations and Admixture von Sistonen, P., Virtaranta-Knowles, K., Denisova, R., Kučinskas, V., Ambrasiene, D., Beckman, L.

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Tautosakos rinkinys. LTR 45 von Tauroza, Jonas Kučinskas (Grinių k.), Olesia Poškytė, Polė Valkauskytė, Vladas Adomavičius (Panavara), Romaldas Draudvilas, Eliutė Kamariauskytė

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Travelling with cystic fibrosis: Recommendations for patients and care team members von Hirche, T.O, Bradley, J, d'Alquen, D, De Boeck, K, Dembski, B, Elborn, J.S, Gleiber, W, Lais, C, Malfroot, A, Wagner, T.O.F

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The LWb Blood Group as a Marker of Prehistoric Baltic Migrations and Admixture1 von Sistonen, P, Virtaranta-Knowles, K, Denisova, R, Kucinskas, V, Ambrasiene, D, Beckman, L

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Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language von Rosser, Z.H, Zerjal, T, Hurles, M.E, Adojaan, M, Alavantic, D, Amorim, A, Amos, W, Armenteros, M, Arroyo, E, Barbujani, G, Beckman, G, Beckman, L, Bertranpetit, J, Bosch, E, Bradley, D.G, Brede, G, Cooper, Graeme, Côrte-Real, H.B, de Knijff, P, Decorte, Ronny, Dubrova, Y.E, Evgrafov, O, Gilissen, A, Glisic, S, Gölge, M, Hill, E.W, Jeziorowska, A, Kalaydjieva, L, Kayser, M, Kivisild, T, Kravchenko, S.A, Krumina, A, Kucinskas, V, Lavinha, J, Livshits, L.A, Malaspina, P, Maria, S, McElreavey, K, Meitinger, T.A, Mikelsaar, A.V, Mitchell, R.J, Nafa, K, Nicholson, J, Nørby, S, Pandya, A, Parik, J, Patsalis, P.C, Pereira, L, Peterlin, B, Pielberg, G, Prata, M.J, Previderé, C, Roewer, L, Rootsi, S, Rubinsztein, D.C, Saillard, J, Santos, F.R, Stefanescu, G, Sykes, B.C, Tolun, A, Villems, R, Tyler-Smith, C, Jobling, M.A

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Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene : a cystic fibrosis mutation of slavic origin common in Central and East Europe von DÖRK, T, MACEK, M. JR, ZEMKOVA, D, GINTER, E, PETROVA, N. V, IVASCHENKO, T, BARANOV, V, WITT, M, POGORZELSKI, A, BAL, J, ZEKANOWSKY, C, WAGNER, K, MEKUS, F, STUHRMANN, M, BAUER, I, SEYDEWITZ, H. H, NEUMANN, T, JAKUBICZKA, S, KRAUS, C, THAMM, B, NECHIPORENKO, M, LIVSHITS, L, MOSSE, N, TÜMMLER, B, TSUKERMAN, G, KADASI, L, RAVNIK-GLAVAC, M, GLAVAC, D, KOMEL, R, VOUK, K, KUCINSKAS, V, KRUMINA, A, TEDER, M, KOCHEVA, S, TZOUNTZOURIS, J, EFREMOV, G. D, ONAY, T, KIRDAR, B, MALONE, G, SCHWARZ, M, ZHAOQING ZHOU, FRIEDMAN, K. J, CARLES, S, CLAUSTRES, M, BOZON, D, CASALS, T, VERLINGUE, C, FEREC, C, TZETIS, M, KANAVAKIS, E, CUPPENS, H, BOMBIERI, C, PIGNATTI, P. F, SANGIUOLO, F, JORDANOVA, A, KUSIC, J, KREBSOVA, A, KOUDOVA, M, SAKMARYOVA, I. SR, VAVROVA, V

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