Výsledky vyhledávání - Hélène Verhelst

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  1. 1
    Treatment and long term outcome in West syndrome: The clinical reality. A multicentre follow up study

    Treatment and long term outcome in West syndrome: The clinical reality. A multicentre follow up study Autor Lieven Lagae, Hélène Verhelst, Berten Ceulemans, Linda De Meırleır, Marie‐Cécile Nassogne, V. de Borchgrave, Marc D’Hooghe, Martine Foulon, Patrick Van Bogaert

    Vydáno 2010
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  2. 2
    Steroids in intractable childhood epilepsy: Clinical experience and review of the literature

    Steroids in intractable childhood epilepsy: Clinical experience and review of the literature Autor Helene Verhelst, Paul Boon, Gunnar Buyse, Berten Ceulemans, Marc D’Hooghe, Linda De Meırleır, Danièle Hasaerts, Anna Jansen, Lieven Lagae, Alfred Meurs, Rudy Van Coster, Kristl Vonck

    Vydáno 2005
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  3. 3
    Blue Native Polyacrylamide Gel Electrophoresis: A Powerful Tool in Diagnosis of Oxidative Phosphorylation Defects

    Blue Native Polyacrylamide Gel Electrophoresis: A Powerful Tool in Diagnosis of Oxidative Phosphorylation Defects Autor Rudy Van Coster, Joél Smet, Edith George, Linda De Meırleır, Sara Seneca, Johan Van Hove, Guillaume Sébire, Hélène Verhelst, Jan De Bleecker, Bruno Van Vlem, Patrick Verloo, Jules G. Leroy

    Vydáno 2001
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  4. 4
    Paediatric acute disseminated encephalomyelitis followed by optic neuritis: disease course, treatment response and outcome

    Paediatric acute disseminated encephalomyelitis followed by optic neuritis: disease course, treatment response and outcome Autor Yu Yi M. Wong, Yael Hacohen, Thaís Armangué, Evangeline Wassmer, Hélène Verhelst, Cheryl Hemingway, E Daniëlle van Pelt, Coriene E. Catsman‐Berrevoets, Rogier Q. Hintzen, Kumaran Deiva, Ming Lim, Kevin Rostásy, Rinze F. Neuteboom

    Vydáno 2018
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  5. 5
    Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals

    Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals Autor Emilia K. Bijlsma, A.C.J. Gijsbers, Janneke Schuurs-Hoeijmakers, Arie van Haeringen, Dietje E. Fransen van de Putte, Britt‐Marie Anderlid, Johanna Lundin, Pablo Lapunzina, L.A. Pérez Jurado, Barbara Delle Chiaie, Bart Loeys, Björn Menten, Anna Oostra, Hélène Verhelst, David J. Amor, Damien L. Bruno, A.J. van Essen, Roel Hordijk, Birgit Sikkema‐Raddatz, K. T. Verbruggen, M.C.J. Jongmans, Rolph Pfundt, H.M. Reeser, M.H. Breuning, Claudia Ruivenkamp

    Vydáno 2009
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  6. 6
    Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections

    Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections Autor Benson Ogunjimi, Shen‐Ying Zhang, Katrine B. Sørensen, Kristian Alsbjerg Skipper, Madalina E. Carter-Timofte, Gaspard Kerner, Stefanie Luecke, Thaneas Prabakaran, Yujia Cai, Josephina Meester, Esther Bartholomeus, Nikhita Bolar, Geert Vandeweyer, Charlotte Claes, Yasmine Sillis, Lazaro Lorenzo, Raffaele A. Fiorenza, Soraya Boucherit, Charlotte Dielman, Steven Heynderickx, George Elias, Andrea Kurotova, Ann Vander Auwera, Lieve Verstraete, Lieven Lagae, Hélène Verhelst, Anna Jansen, José Ramet, Arvid Suls, Evelien Smits, Berten Ceulemans, Lut Van Laer, Genevieve Plat Wilson, Jonas H Kreth, Capucine Pïcard, Horst von Bernuth, Joël Fluss, Stéphane Chabrier, Laurent Abel, Geert Mortier, Sébastien Fribourg, Jacob Giehm Mikkelsen, Jean‐Laurent Casanova, Søren R. Paludan, Trine H. Mogensen

    Vydáno 2017
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  7. 7
    <i>STXBP1</i> encephalopathy

    <i>STXBP1</i> encephalopathy Autor Hannah Stamberger, Marina Nikanorova, Marjolein H. Willemsen, Patrizia Accorsi, Marco Angriman, Hartmut Baier, Ira Benkel-Herrenbrueck, Valérie Benoît, M Budetta, Almuth Caliebe, Gaetano Cantalupo, Giuseppe Capovilla, Gianluca Casara, Carolina Courage, Marie Deprez, Anne Destrèe, Robertino Dilena, Corrie E. Erasmus, Madeleine Fannemel, Roar Fjær, Lucio Giordano, Katherine L. Helbig, Henrike Heyne, Joerg Klepper, Gerhard Kluger, Damien Lederer, Monica Lodi, Oliver Maier, Andreas Merkenschlager, Nina Michelberger, Carlo Minetti, Hiltrud Muhle, Judith Phalin, Keri Ramsey, Antonino Romeo, Jens Schallner, Ina Schanze, Marwan Shinawi, Kristel Sleegers, Katalin Štěrbová, Steffen Syrbe, Monica Traverso, Andreas Tzschach, Peter Uldall, Rudy Van Coster, Hélène Verhelst, Maurizio Viri, Susan Winter, Markus Wolff, Martin Zenker, Leonardo Zoccante, Peter De Jonghe, Ingo Helbig, Pasquale Striano, Johannes R. Lemke, Rikke S. Møller, Sarah Weckhuysen

    Vydáno 2016
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    Revisão
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  8. 8
    Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848

    Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848 Autor Magdalena Koczkowska, Yunjia Chen, Tom Callens, Alicia Gomes, Angela Sharp, Sherrell Johnson, Meng-Chang Hsiao, Zhenbin Chen, Meena Balasubramanian, Christopher Barnett, Troy A. Becker, Shay Ben‐Shachar, Débora Romeo Bertola, Jaishri O. Blakeley, Emma Burkitt‐Wright, Alison Callaway, Melissa Crenshaw, Karin Soares Cunha, Mitch Cunningham, Daniela D’Agostino, Karin Dahan, Alessandro De Luca, Anne Destrèe, Radhika Dhamija, Marica Eoli, D. Gareth Evans, Patricia Galvin‐Parton, Jaya K. George‐Abraham, Karen W. Gripp, José Guevara-Campos, Neil A. Hanchard, Concepción Hernández-Chico, LaDonna Immken, Sandra Janssens, Kristi Jones, Beth Keena, Aaina Kochhar, Jan Liebelt, Arelis Martir-Negron, Maurice J. Mahoney, Isabelle Maystadt, Carey McDougall, Meriel McEntagart, Nancy J. Mendelsohn, David T. Miller, Geert Mortier, Jenny Morton, John Pappas, Scott R. Plotkin, Dinel Pond, Kenneth N. Rosenbaum, Karol Rubin, Laura Russell, Lane Rutledge, Veronica Saletti, Rhonda Schonberg, Allison Schreiber, Meredith Seidel, Elizabeth Siqveland, David W. Stockton, Eva Trevisson, Nicole J. Ullrich, Meena Upadhyaya, Rick van Minkelen, Hélène Verhelst, Margaret R. Wallace, Yoon Sim Yap, Elaine H. Zackai, Jonathan Zonana, Vickie Zurcher, Kathleen Claes, Yolanda Martín, Bruce R. Korf, Eric Legius, Ludwine Messiaen

    Vydáno 2017
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  9. 9
    Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS): a multicentre, double-blind, phase 3, randomised, placebo-controlled trial

    Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS): a multicentre, double-blind, phase 3, randomised, placebo-controlled trial Autor Tanuja Chitnis, Brenda Banwell, Ludwig Kappos, Douglas L. Arnold, Kıvılcım Gücüyener, Kumaran Deiva, Н. В. Скрипченко, Liying Cui, Stéphane Saubadu, Wenruo Hu, Myriam Bénamor, Annaig Le-Halpere, Philippe Truffinet, Marc Tardieu, Bénédicte Dubois, Hélène Verhelst, Veneta Bojinova-Tchamova, Jean K. Mah, Liying Cui, Fang Fang, Yunpeng Hao, Jiang Li, Ling Li, Ding-An Mao, Wei Qiu, Guojun Tan, Ye Wu, Meini Zhang, Hongyu Zhou, Shuizhen Zhou, Katrin Gross‐Paju, Emmanuel Cheuret, Kumaran Deiva, Giles Edan, Sandra Vukusic, George Chrousos, Dimitrios Zafeiriou, Anat Achiron, Adi Vaknin‐Dembinsky, Bassem Yamout, Jūratė Laurynaitienė, Nerija Vaičienė-Magistris, V. Bojkovski, Vesna Trajkova, S. Chaouki, Najib Kissani, Rinze F. Neuteboom, Filipe Palavra, Anna N. Belova, Alexey Boyко, Evgeny Evdoshenko, Е. И. Каирбекова, Nadezhda Malkova, M. V. Shumilina, Natalya Skripchenko, Dimitrije Nikolić, José Meca-Lallana, Chahnez Triki, Mhiri Chokri, Riadh Gouider, Banu Anlar, Kıvılcım Gücüyener, Ayşe Semra Hız, Egemen İdıman, Recai Türkoğlu, Zühal Yapıcı, Ünsal Yılmaz, Lyudmyla Tantsura, N. N. Voloshyna, Ming Lim, Evangeline Wassmer, Mark Cascione, Tanuja Chitnis, Christopher LaGanke, Kevin M. Rathke, John Scagnelli

    Vydáno 2021
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  10. 10
    Clinical trials of disease-modifying agents in pediatric MS

    Clinical trials of disease-modifying agents in pediatric MS Autor Emmanuelle Waubant, Brenda Banwell, Evangeline Wassmer, Maria Pia Sormani, Maria Pia Amato, Rogier Hintzen, Lauren Krupp, Kevin Rostásy, Sílvia Tenembaum, Tanuja Chitnis, Gregory Aaen, Elhachmia Ait Ben Adou, Raed Alroughani, Veronica Gonzalez Alvarez, Maria Anagnostouli, Banu Anlar, Thaís Armangué, Georgina Arrambide, Damiano Baroncini, R Ts Bembeeva, Leslie Benson, Neli Bizjak, Astrid Blaschek, Alexey Boyко, J. Nicholas Brenton, Wolfgang Brück, Bruna Klein da Costa, Dominique Dive, Christiane Elpers, Massimo Filippi, Manuela de Oliveira Fragomeni, Eva Havrdová, Cheryl Hemingway, Barbara Kornek, Kumaran Deiva, Adrian R. Lacy, Zuzana Libá, Ming Lim, Tim Lotze, Jean K. Mah, Naila Makhani, Soe Mar, Kyla A. McKay, Shay Menascu, Lucia Moiola, Patricia Mulero, Moustapha Ndiaye, Rinze F. Neuteboom, Jayne Ness, Enedina Maria Lobato de Oliveira, Scott Otallah, Francesco Patti, José Albino da Paz, Carlos A. Pérez, Daniela Pohl, Anne‐Louise Ponsonby, Mary Rensel, Maria A. Rocca, Nick Rijke, Moses Rodriguez, Ian Rossman, Hiroshi Sakuma, Teri Schreiner, Ángeles Schteinschnaider, E. Morghen Sikes, Isabella Laura Simone, Michael Sweeney, Jan Mendelt Tillema, Regina M. Troxell, Hélène Verhelst, Leidi Vilchez, Liesbeth De Waele, Bianca Weinstock‐Guttman, Colin Wilbur, Mikaeloff Yann, E. Ann Yeh, Dimitrios Zafeiriou

    Vydáno 2019
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  11. 11
    Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita

    Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita Autor Annie Laquerrière, Dana Jaber, Emanuela Abiusi, Jérôme Maluenda, Dan Mejlachowicz, Alexandre Vivanti, Klaus Dieterich, Radka Stoeva, Loïc Quevarec, Flora Nolent, Valérie Biancalana, Philippe Latour, Damien Sternberg, Yline Capri, Alain Verloès, Bettina Bessières, Laurence Lœuillet, Tania Attié‐Bitach, Jéléna Martinovic, Sophie Blesson, Florence Petit, Claire Bénéteau, Sandra Whalen, Florent Marguet, Jérôme Bouligand, Delphine Héron, Géraldine Viot, Jeanne Amiel, Daniel Amram, Céline Bellesme, Martine Bucourt, Laurence Faivre, Pierre‐Simon Jouk, Suonavy Khung, Sabine Sigaudy, Anne‐Lise Delezoide, Alice Goldenberg, Marie‐Line Jacquemont, Laëtitia Lambert, Valérie Layet, Stanislas Lyonnet, Arnold Münnich, Lionel Van Maldergem, Juliette Piard, Fabien Guimiot, P. Landrieu, Pascaline Létard, Fanny Pelluard, Laurence Perrin, Marie‐Hélène Saint‐Frison, Haluk Topaloğlu, Laetitia Trestard, Catherine Vincent‐Delorme, Helge Amthor, Christine Barnérias, Alexandra Benachi, Éric Bieth, Elise Boucher, Valérie Cormier‐Daire, Andrée Delahaye‐Duriez, Isabelle Desguerre, B. Eymard, Christine Francannet, Sarah Grotto, Didier Lacombe, Fanny Laffargue, Marine Legendre, Dominique Martin–Coignard, André Mégarbané, Sandra Mercier, Mathilde Nizon, Luc Rigonnot, Fabienne Prieur, Chloé Quēlin, Hanitra Ranjatoelina-Randrianaivo, Nicoletta Resta, Annick Toutain, Hélène Verhelst, Marie Vincent, Estelle Colin, Catherine Fallet‐Bianco, Michèle Granier, R Grigorescu, Julien Saada, Marie Gonzalès, Anne Guiochon‐Mantel, Jean‐Louis Bessereau, Marcel Tawk, Marta Gut, Cyril Gitiaux, Judith Melki

    Vydáno 2021
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  12. 12
    Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy

    Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy Autor Holger Hengel, Célia Bosso-Lefèvre, George Grady, Emmanuelle Szenker‐Ravi, Hankun Li, Sarah B. Pierce, Élise Lebigot, Thong-Teck Tan, Michelle Eio, Gunaseelan Narayanan, Kagistia Hana Utami, Monica Yau, Nader Handal, Werner Deigendesch, Reinhard Keimer, Hiyam Marzouqa, Meral Gunay‐Aygun, Michael Muriello, Hélène Verhelst, Sarah Weckhuysen, Sonal Mahida, Sakkubai Naidu, Terrence Thomas, Jiin Ying Lim, Ee Shien Tan, Damien Haye, Michèl A.A.P. Willemsen, Renske Oegema, Wendy G. Mitchell, Tyler Mark Pierson, Marisa V. Andrews, Marcia Willing, Lance H. Rodan, Tahsin Stefan Barakat, Marjon van Slegtenhorst, Ralitza H. Gavrilova, Diego Martinelli, Tal Gilboa, Abdullah Tamim, Mais Hashem, Moeenaldeen AlSayed, Maha Abdulrahim, Mohammed Al‐Owain, Ali Awaji, Adel Mahmoud, Eissa Faqeih, Ali Al Asmari, Sulwan Algain, Lamyaa Jad, Hesham Aldhalaan, Ingo Helbig, David A. Koolen, Angelika Rieß, Ingeborg Kraegeloh‐Mann, Peter Bauer, Süleyman Gülsüner, Hannah Stamberger, Alvin Yu Jin Ng, Sha Tang, Sumanty Tohari, Boris Keren, Laura Schultz‐Rogers, Eric W. Klee, Sabina Barresi, Marco Tartaglia, Hagar Mor‐Shaked, Sateesh Maddirevula, Amber Begtrup, Aida Telegrafi, Rolph Pfundt, Rebecca Schüle, Brian Ciruna, Carine Bonnard, Mahmoud A. Pouladi, James Stewart, Adam Claridge‐Chang, Dirk J. Lefeber, Fowzan S. Alkuraya, Ajay S. Mathuru, Byrappa Venkatesh, Joseph Barycki, Melanie A. Simpson, Saumya Shekhar Jamuar, Lüdger Schöls, Bruno Reversade

    Vydáno 2020
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  13. 13
    Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia

    Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia Autor Darius Ebrahimi‐Fakhari, Julian Teinert, Robert Behne, Miriam Wimmer, Angelica D’Amore, Kathrin Eberhardt, Barbara Brechmann, M. L. ZIEGLER, Dana M. Jensen, Premsai Nagabhyrava, Gregory Geisel, Erin Carmody, Uzma Shamshad, Kira A. Dies, Christopher J. Yuskaitis, Catherine L. Salussolia, Daniel Ebrahimi‐Fakhari, Toni S. Pearson, Afshin Saffari, Andreas Ziegler, Stefan Kölker, Jens Volkmann, Antje Wiesener, David Bearden, Shenela Lakhani, Devorah Segal, Anaita Hegde, Andrea Martinuzzi, Jennifer Hirst, Seth J. Perlman, Yoshihisa Takiyama, Georgia Xiromerisiou, Katharina Vill, William O. Walker, Anju Shukla, Rachana Dubey Gupta, Niklas Dahl, Ayşe Aksoy, Hélène Verhelst, Mauricio R. Delgado, Radka Kremlíková Pourová, Abdelrahim A. Sadek, Nour Elkhateeb, Lubov Blumkin, Alejandro Brea‐Fernández, David Dacruz-Álvarez, Thomas Smol, Jamal Ghoumid, Diego Miguel, Constanze Heine, Jan-Ulrich Schlump, Hendrik Langen, Jonathan Baets, Saskia Bulk, Hossein Darvish, Somayeh Bakhtiari, Michael C. Kruer, Elizabeth Lim-Melia, Nur Aydınli̇, Yasemin Alanay, Omnia Fathy El-Rashidy, Sheela Nampoothiri, Chirag Patel, Christian Beetz, Peter Bauer, Grace Yoon, M Guillot, Steven P. Miller, Thomas Bourinaris, Henry Houlden, Laura Robelin, Mathieu Anheim, Abdullah Alamri, Adel Mahmoud, Soroor Inaloo, Parham Habibzadeh, Mohammad Ali Faghihi, Anna Jansen, Stefanie Brock, Agathe Roubertie, Basil T. Darras, Pankaj B. Agrawal, Filippo M. Santorelli, Joseph G. Gleeson, Maha S. Zaki, Sarah Sheikh, James T. Bennett, Mustafa Şahin

    Vydáno 2019
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  14. 14
    Everolimus for treatment-refractory seizures in TSC

    Everolimus for treatment-refractory seizures in TSC Autor David Neal Franz, John A. Lawson, Zühal Yapıcı, Hiroko Ikeda, Tilman Polster, Rima Nabbout, Paolo Curatolo, Petrus J. de Vries, Dennis Dlugos, Maurizio Voi, Jenna Fan, A. Thareau Vaury, Diana Pelov, Jacqueline A. French, Ángeles Schteinschnaider, Ignacio Sfaello, John A. Lawson, Lakshmi Nagarajan, Simon Harvey, Hélène Verhelst, Liesbeth De Waele, Patrick Van Bogaert, Riëm El Tahry, Anna Jansen, Mary Connolly, Philippe Major, Alberto Velez, Orlando Carreno, Juan Carlos Gómez, Jakob Christensen, Louis Vallée, Sylvie Nguyen The Tich, Mathieu Milh, Anne de Saint Martin, Patrick Berquin, Dorothée Ville, Adelheid Wiemer‐Kruel, Christoph Hertzberg, Gert Wiegand, Tilman Polster, Antigone Papavasiliou, Meropi Tzoufi, András Fogarasi, Zsuzsanna Gyorsok, Péter Diószeghy, David William Webb, G. Bartalini, Giuseppe Gobbi, Maria Paola Canevini, Pierangelo Veggiotti, M. G. Baglietto, Anna Teresa Giallonardo, Nicola Laforgia, Raffaele Falsaperla, Hiroko Ikeda, Shin Nabatame, Hisashi Kawawaki, Harumi Yoshinaga, Masaya Kubota, Yasuhiro Suzuki, Hugo Ceja Moreno, Bernard A. Zonnenberg, Marie‐Claire Y. de Wit, Marian Majoie, Marit Bjoernvold, Sergiusz Jóźwiak, Kijoong Kim, Heung Dong Kim, Munhyang Lee, Taesung Ko, Elena Belousova, Nataliya A. Ermolenko, И. Е. Повереннова, Liudmila Kuzenkova, Maria Luz Ruiz Falco Rojas, Adolfo López de Munaín, Juan Rodríguez Uranga, Vicente Villanueva, Pi‐Chuan Fan, Chao Huang, Ying‐Chao Chang, Charcrin Nabangchang, Krisnachai Chomtho, Surachai Likasitwattanakul, Lunliya Thampratankul, Zühal Yapıcı, Ayşe Serdaroğlu, Banu Ahlar, Sarah Aylett, Archana Desurkar, Clare Johnston, Matthias J. Koepp, Hannah R. Cock, Alasdair Parker, Dougall McCorry, Richard Appleton, Steven Sparagana, Katherine S. Taub, Michael Frost, Colin Roberts

    Vydáno 2018
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  15. 15
    Genotype-phenotype correlations in <i>SCN8A</i>-related disorders reveal prognostic and therapeutic implications

    Genotype-phenotype correlations in <i>SCN8A</i>-related disorders reveal prognostic and therapeutic implications Autor Katrine M. Johannesen, Yuanyuan Liu, Mahmoud Koko, Cathrine E. Gjerulfsen, Lukas Sonnenberg, Julian Schubert, Christina Fenger, Ahmed Eltokhi, Maert Rannap, Nils A. Koch, Stephan Lauxmann, Johanna Krüger, Josua Kegele, Laura Canafoglia, Silvana Franceschetti, Patrick May, Johannes Rebstock, Pia Zacher, Susanne Ruf, Michael Alber, Katalin Štěrbová, Petra Laššuthová, Markéta Vlčková, Johannes R. Lemke, Konrad Platzer, Ilona Krey, Constanze Heine, Dagmar Wieczorek, Judith Kroell-Seger, Caroline Lund, Karl Martin Klein, P Y Billie Au, Jong M. Rho, Alice Ho, Silvia Masnada, Pierangelo Veggiotti, Lucio Giordano, Patrizia Accorsi, Christina Engel Hoei‐Hansen, Pasquale Striano, Federico Zara, Hélène Verhelst, J. Verhoeven, Hilde M. H. Braakman, Bert van der Zwaag, Aster V. E. Harder, Eva H. Brilstra, Manuela Pendziwiat, Sebastian Lebon, María Vaccarezza, Ngọc Minh Lê, Jakob Christensen, Sabine Grønborg, Stephen W. Scherer, Jennifer Howe, Walid Fazeli, Katherine B. Howell, Richard J. Leventer, Chloe Stutterd, Sonja Walsh, Marion Gérard, Bénédicte Gérard, Sara Matricardi, Claudia Bonardi, Stefano Sartori, Andrea Berger, Dorota Hoffman‐Zacharska, Massimo Mastrangelo, Francesca Darra, Arve Vøllo, M. Mahdi Motazacker, Phillis Lakeman, Mathilde Nizon, Cornelia Betzler, Cécilia Altuzarra, Roseline Caume, Agathe Roubertie, Philippe Gélisse, Carla Marini, Renzo Guerrini, Frédéric Bilan, Daniel Tibussek, Margarete Koch‐Hogrebe, Μ. Scott Perry, Shoji Ichikawa, Е. Л. Дадали, Artem Sharkov, Irina Mishina, M. O. Abramov, Ilya Kanivets, С. А. Коростелев, Sergey I. Kutsev, Karen E. Wain, Nancy Eisenhauer, Monisa Wagner, Juliann M. Savatt, Karen Müller‐Schlüter, Haim Bassan, Artem Borovikov, Marie‐Cécile Nassogne

    Vydáno 2021
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