खोज परिणाम - Annette Hackenberg

  • प्रदर्शित 1 - 16 परिणाम 16
परिणाम को परिष्कृत करें
  1. 1
    Feasibility, safety, and outcome of recanalization treatment in childhood stroke

    Feasibility, safety, and outcome of recanalization treatment in childhood stroke द्वारा Sandra Bigi, Andrea Dulcey, Jan Gralla, Corrado Bernasconi, Amber Melliger, Alexandre Datta, Marcel Arnold, Johannes Kaesmacher, Joël Fluss, Annette Hackenberg, Oliver Maier, Johannes Weber, Claudia Poloni, Urs Fischer, Maja Steinlin

    प्रकाशित 2018
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    Artigo
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  2. 2
    Factors affecting cognitive outcome in early pediatric stroke

    Factors affecting cognitive outcome in early pediatric stroke द्वारा Martina Studer, Eugen Boltshauser, Andrea Mori, Alexandre Datta, Joël Fluss, Danielle Mercati, Annette Hackenberg, Elmar Keller, Oliver Maier, Jean‐Pierre Marcoz, Gianpaolo Ramelli, Claudia Poloni, Regula Schmid, Thomas Schmitt‐Mechelke, E Wehrli, Theda Heinks, Maja Steinlin

    प्रकाशित 2014
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    Artigo
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  3. 3
    Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes

    Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes द्वारा Anaïs Begemann, Mario A. Acuña, Markus Zweier, Marie Vincent, Katharina Steindl, Ruxandra Bachmann‐Gagescu, Annette Hackenberg, Lucia Abela, Barbara Plecko, Judith Kroell-Seger, Alessandra Baumer, Kazuhiro Yamakawa, Yushi Inoue, Reza Asadollahi, Heinrich Sticht, Hanns Ulrich Zeilhofer, Anita Rauch

    प्रकाशित 2019
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    Artigo
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  4. 4
    Postoperative brain volumes are associated with one-year neurodevelopmental outcome in children with severe congenital heart disease

    Postoperative brain volumes are associated with one-year neurodevelopmental outcome in children with severe congenital heart disease द्वारा Eliane Meuwly, Maria Feldmann, Walter Knirsch, Michael von Rhein, Kelly Payette, Hitendu Dave, Ruth O’ Gorman Tuura, Raimund Kottke, Cornelia Hagmann, Beatrice Latal, András Jakab, Rabia Liamlahi, Annette Hackenberg, Oliver Kretschmar, Christian J. Kellenberger, Christoph Bürki, Markus Weiß

    प्रकाशित 2019
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    Artigo
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  5. 5
    Blood DNA methylation provides an accurate biomarker of <i>KMT2B</i>-related dystonia and predicts onset

    Blood DNA methylation provides an accurate biomarker of <i>KMT2B</i>-related dystonia and predicts onset द्वारा Nazanin Mirza‐Schreiber, Michael Zech, Rory Wilson, Theresa Brunet, Matias Wagner, Robert Jech, Sylvia Boesch, Matěj Škorvánek, Ján Necpál, David Weise, Sandrina Weber, Brit Mollenhauer, Claudia Trenkwalder, Esther M. Maier, Ingo Borggraefe, Katharina Vill, Annette Hackenberg, Veronika Pilshofer, Urania Kotzaeridou, Eva Maria Christina Schwaibold, Julia Hoefele, Mélanie Waldenberger, Christian Gieger, Annette Peters, Thomas Meitinger, Barbara Schormair, Juliane Winkelmann, Konrad Oexle

    प्रकाशित 2021
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    Artigo
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  6. 6
    The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study

    The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study द्वारा Sorina Mihaela Papuc, Lucia Abela, Katharina Steindl, Anaïs Begemann, Thomas L. Simmons, Bernhard Schmitt, Markus Zweier, Beatrice Oneda, Eileen Socher, Lisa M. Crowther, Gabriele Wohlrab, Laura Gogoll, Martin Poms, Michelle Seiler, Michael Papik, Rosa Baldinger, Alessandra Baumer, Reza Asadollahi, Judith Kroell-Seger, Regula Schmid, T. Iff, Thomas Schmitt‐Mechelke, K. Otten, Annette Hackenberg, Marie‐Claude Addor, Andrea Klein, Silvia Azzarello‐Burri, Heinrich Sticht, Pascal Joset, Barbara Plecko, Anita Rauch

    प्रकाशित 2018
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    Artigo
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  7. 7
    Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients

    Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients द्वारा Sven Jarius, Christian Lechner, Eva Wendel, Matthias Baumann, Markus Breu, Mareike Schimmel, Michael Karenfort, Adela Della Marina, Andreas Merkenschlager, Charlotte Thiels, Astrid Blaschek, Michela Salandin, Steffen Leiz, Frank Leypoldt, Alexander Pschibul, Annette Hackenberg, Andreas Hahn, Steffen Syrbe, Jurgis Strautmanis, Martin Häusler, Peter Krieg, Astrid Eisenkölbl, Johannes Stoffels, Matthias Eckenweiler, Ilya Ayzenberg, Jürgen Haas, Romana Höftberger, Ingo Kleiter, Mirjam Korporal‐Kuhnke, Marius Ringelstein, Klemens Ruprecht, Nadja Siebert, Kathrin Schanda, Orhan Aktaş, Friedemann Paul, Markus Reindl, Brigitte Wildemann, Kevin Rostásy

    प्रकाशित 2020
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    Artigo
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  8. 8
    Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2

    Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2 द्वारा Derek Neilson, Mark D. Adams, Caitlin M.D. Orr, Deborah K. Schelling, Robert M. Eiben, Douglas S. Kerr, Jane Anderson, Alexander G. Bassuk, Ann Bye, Anne-Marie Childs, Antonia Clarke, Yanick J. Crow, Maja Di Rocco, Christian Dohna‐Schwake, Gregor Dueckers, Alfonso Fasano, Artemis Gika, Dimitris Gionnis, Mark Gorman, Padraic J. Grattan‐Smith, Annette Hackenberg, Alice Kuster, Markus Lentschig, Eduardo López‐Laso, Elysa J. Marco, Sotiria Mastroyianni, Julie Perrier, Thomas Schmitt‐Mechelke, Serenella Servidei, Angeliki Skardoutsou, Peter Uldall, Marjo S. van der Knaap, Karrie Goglin, David L. Tefft, Cristin Aubin, Philip L. De Jager, David A. Hafler, Matthew L. Warman

    प्रकाशित 2009
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    Artigo
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  9. 9
    Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome

    Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome द्वारा Eva Wendel, Helen Sophie Thonke, Annikki Bertolini, Matthias Baumann, Astrid Blaschek, Andreas Merkenschlager, Michael Karenfort, Barbara Kornek, Christian Lechner, Daniela Pohl, Martin Pritsch, Kathrin Schanda, Mareike Schimmel, Charlotte Thiels, Stephan Waltz, Gert Wiegand, Banu Anlar, Nina Barišić, Christian U. Blank, Markus Breu, Philip J. Broser, Adela Della Marina, Katharina Diepold, Matthias Eckenweiler, Astrid Eisenkölbl, Michael Freilinger, U Gruber‐Sedlmayr, Annette Hackenberg, T. Iff, Ellen Knierim, Johannes Koch, G Kutschke, Steffen Leiz, Grischa Lischetzki, Margherita Nosadini, Alexander Pschibul, Edith Reiter‐Fink, Doris Rohrbach, Michela Salandin, Stefano Sartori, Jan-Ulrich Schlump, Johannes Stoffels, Jurgis Strautmanis, Daniel Tibussek, Victoria Tüngler, N Utzig, Markus Reindl, Kevin Rostásy

    प्रकाशित 2022
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    Artigo
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  10. 10
    The Swiss Brain Health Plan 2023–2033

    The Swiss Brain Health Plan 2023–2033 द्वारा Claudio L. Bassetti, Mirjam R. Heldner, Kristina Adorjan, Emiliano Albanese, Gilles Allali, Marcel Arnold, Indrit Bègue, Murielle Bochud, Andrew Chan, Kim Do Cuenod, Renaud Du Pasquier, Bogdan Draganski, Mohamed Eshmawey, Ansgar Felbecker, Urs Fischer, Annika Frahsa, Giovanni B. Frisoni, Harald Großmann, Raphaël Guzman, Annette Hackenberg, Martin Hatzinger, Marcus Herdener, Albert Hofman, Andrea M. Humm, Simon Jung, Michael Kaess, Christian Kätterer, Jürg Kesselring, Andrea Klein, Andreas Kleinschmidt, Stefan Klöppel, Nora Kronig, Karl‐Olof Lövblad, Anita Lüthi, Philippe Lyrer, Iris‐Katharina Penner, Caroline Pot, Quinn Rafferty, Péter Sándor, Hakan Sarıkaya, Erich Seifritz, Shayla Smith, Lukas Sveikata, Thomas C. Südhof, Barbara Tettenborn, Paul G. Unschuld, A. Vicedo Cabrera, Susanne Walitza, Sebastian Walther, Isabel Wancke, Michael Weller, Susanne Wegener, Petra Zalud, Thomas Zeltner, D. De Zutter, Luca Remonda

    प्रकाशित 2023
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    Artigo
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  11. 11
    Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study

    Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study द्वारा Ferdy S. van Geest, Stefan Groeneweg, Erica L.T. van den Akker, I. Bacos, Diana Bârcă, Sjoerd A.A. van den Berg, Enrico Bertini, Doris Brunner, Nicola Brunetti‐Pierri, Marco Cappa, Gerarda Cappuccio, Krishna Chatterjee, Alexander Chesover, Peter Christian, Régis Coutant, Dana Craiu, Patricia Crock, Cheyenne Dewey, Alice Dica, Paul Dimitri, Rachana Dubey, Anina Enderli, Jan Fairchild, Jonathan Gallichan, Luigi Garibaldi, Belinda George, Annette Hackenberg, Bianka Heinrich, Tony Huynh, Anna Kłosowska, Amy Lawson‐Yuen, M Linder-Lucht, Greta Lyons, Felipe Monti Lora, Carla Moran, Katalin Eszter Müller, Laura Paone, Praveen George Paul, Michel Polak, Francesco Porta, Christina Reinauer, Yolanda B. de Rijke, Rowen Seckold, tuba seven menevse, Peter Simm, Anna Simon, Marco Spada, Athanasia Stoupa, Lilla Szeifert, Davide Tonduti, Hans van Toor, Serap Turan, Joel A. Vanderniet, Monique de Waart, Ronald van der Wal, Adri van der Walt, Anne-Marie van Wermeskerken, Jolanta Wierzba, Federica Zibordi, Amnon Zung, Robin P. Peeters, W. Edward Visser

    प्रकाशित 2021
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    Artigo
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  12. 12
    Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystonia

    Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystonia द्वारा Michael Zech, Ivana Dzinovic, Matěj Škorvánek, Philip Harrer, Ján Necpál, Robert Kopajtich, Volker Kittke, Erik Tilch, Chen Zhao, Eugenia Tsoma, Ugo Sorrentino, Elisabetta Indelicato, A. Stehr, Alice Saparov, Lucia Abela, Miriam Adamovičová, Alexandra Afenjar, Birgit Assmann, Janette Baloghová, Matthias Baumann, Riccardo Berutti, Zuzana Brežná, Melanie Brugger, Theresa Brunet, Benjamin Cogné, Isabel Colangelo, Erin Conboy, Ertan Mayatepek, Matthias Eckenweiler, Barbara Garavaglia, Arie Geerlof, Elisabeth Graf, Annette Hackenberg, Denisa Harvanová, Bernhard Haslinger, Petra Havránková, Georg F. Hoffmann, Wibke G. Janzarik, Boris Keren, Miriam Kolníková, Konstantinos Kolokotronis, Zuzana Košutzká, Anne Koy, Martin Krenn, Magdalena Krygier, Katarína Kušíková, Oliver Maier, Thomas Meitinger, Christian Mertes, Ivan Milenković, Edoardo Monfrini, André Mourão, Thomas Musacchio, Mathilde Nizon, Miriam Ostrožovičová, Martin Pavlov, Iva Příhodová, Irena Rektorová, Luigi Romito, Barbora Rybanska, Ariane Sadr‐Nabavi, Susanne Schwenger, Ali Shoeibi, Alexandra Sitzberger, Dmitrii Smirnov, Jana Svantnerova, Raushana Tautanova, Sandra P. Toelle, Olga Ulmanová, Francesco Vetrini, Katharina Vill, Matias Wagner, David Weise, Giovanna Zorzi, Alessio Di Fonzo, Konrad Oexle, Steffen Berweck, Volker Mall, Sylvia Boesch, Barbara Schormair, Holger Prokisch, Robert Jech, H. Mann

    प्रकाशित 2025
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    Artigo
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  13. 13
    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study द्वारा Stefan Groeneweg, van Geest FS, Ayhan Abacı, Alberto Alcantud, Ambegaonkar GP, Armour CM, Parkash A. Bakhtiani, Diana Bârcă, Bertini ES, van Beynum Im, Nicola Brunetti‐Pierri, Massimiliano Bugiani, Marco Cappa, Gerarda Cappuccio, Barbara Castellotti, Carlotta Castiglioni, Krishnarpan Chatterjee, de Coo IFM, Régis Coutant, Dana Craiu, Patricia Crock, Christian DeGoede, Koray Demir, Alice Dica, Paul Dimitri, Anna Dolcetta‐Capuzzo, Dremmen MHG, Rachana Dubey, Anina Enderli, Jan Fairchild, Jonathan Gallichan, Biju George, Gevers EF, Annette Hackenberg, Zita Halász, B. Heinrich, Thao Huynh, Anna Kłosowska, van der Knaap, van der Knoop, Daniel Konrad, Koolen DA, Heiko Krude, Amy Lawson‐Yuen, Jan Lebl, M Linder-Lucht, Lorea CF, Lourenco CM, RJ Lunsing, G Lyons, Jana Malíková, Mancilla EE, Aaron McGowan, Verónica Mericq, Lora FM, Cassandra Moran, Muller Ke, Isabelle Oliver‐Petit, Laura Paone, Paul PG, Michel Polak, Francesco Porta, Poswar FO, Christina Reinauer, Klára Roženková, Menevse TS, Peter Simm, András Simon, Yogesh Preet Singh, Marco Spada, van der Spek J, Stals MAM, Athanasia Stoupa, Subramanian GM, Davide Tonduti, Serkan Turan, den Uil CA, Joel A. Vanderniet, van der Walt A, Wémeau Jl, Jolanta Wierzba, de Wit MY, Nicole I. Wolf, Michael Wurm, Federica Zibordi, Amnon Zung, Nitash Zwaveling‐Soonawala, Visser WE

    प्रकाशित 2021
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    Artigo
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  14. 14
    Monogenic variants in dystonia: an exome-wide sequencing study

    Monogenic variants in dystonia: an exome-wide sequencing study द्वारा Michael Zech, Robert Jech, Sylvia Boesch, Matěj Škorvánek, Sandrina Weber, Matias Wagner, Chen Zhao, Angela Jochim, Ján Necpál, Yasemin Dincer, Katharina Vill, Felix Distelmaier, Malgorzata Stoklosa, Martin Krenn, Stephan Grunwald, Tobias Bock-Bierbaum, Anna Fečíková, Petra Havránková, Jan Roth, Iva Příhodová, Miriam Adamovičová, Olga Ulmanová, Karel Bechyně, Pavlína Danhofer, Branislav Veselý, Vladimír Haň, Petra Pavelekova, Zuzana Gdovinová, Tobias Mantel, Tobias Meindl, Alexandra Sitzberger, Sebastian Schröder, Astrid Blaschek, Timo Roser, Michaela Bonfert, Edda Haberlandt, Barbara Plecko, Birgit Leineweber, Steffen Berweck, T. Herberhold, Berthold Langguth, Jana Švantnerová, Michal Minár, Gonzalo Alonso Ramos-Rivera, Monica H. Wojcik, Sander Pajusalu, Katrin Õunap, Ulrich A. Schatz, Laura Pölsler, Ivan Milenković, Franco Laccone, Veronika Pilshofer, Roberto Colombo, Steffi Patzer, Arcangela Iuso, Julia Vera, M. Troncoso, Fang Fang, Holger Prokisch, Friederike Wilbert, Matthias Eckenweiler, Elisabeth Graf, Dominik S. Westphal, Korbinian M. Riedhammer, Theresa Brunet, Bader Alhaddad, Riccardo Berutti, Tim M. Strom, Martin Hecht, Matthias Baumann, Marc E. Wolf, Aida Telegrafi, Richard Person, Francisca Millan Zamora, Lindsay B. Henderson, David Weise, Thomas Musacchio, Jens Volkmann, Anna Szuto, Jessica Becker, Kirsten Cremer, Thomas Sycha, Fritz Zimprich, Verena Kraus, Christine Makowski, Pedro Gonzalez‐Alegre, Tanya Bardakjian, Laurie J. Ozelius, Annalisa Vetro, Renzo Guerrini, Esther M. Maier, Ingo Borggraefe, Alice Kuster, Saskia B. Wortmann, Annette Hackenberg, Robert Steinfeld, Birgit Assmann, Christian Staufner, Thomas Opladen, Evžen Růžička

    प्रकाशित 2020
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    Artigo
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  15. 15
    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

    Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study द्वारा Stefan Groeneweg, Ferdy S. van Geest, Ayhan Abacı, Alberto Alcantud, Gautam Ambegaonkar, Christine M. Armour, Priyanka Bakhtiani, Diana Bârcă, Enrico Bertini, Ingrid M. van Beynum, Nicola Brunetti‐Pierri, Marianna Bugiani, Marco Cappa, Gerarda Cappuccio, Barbara Castellotti, Claudia Castiglioni, Krishna Chatterjee, I.F.M. de Coo, Régis Coutant, Dana Craiu, Patricia Crock, Christian DeGoede, Korcan Demir, Alice Dica, Paul Dimitri, Anna Dolcetta‐Capuzzo, Marjolein H. G. Dremmen, Rachana Dubey, Anina Enderli, Jan Fairchild, Jonathan Gallichan, Belinda George, Evelien Gevers, Annette Hackenberg, Zita Halász, Bianka Heinrich, Tony Huynh, Anna Kłosowska, Marjo S. van der Knaap, Marieke M van der Knoop, Daniel Konrad, David A. Koolen, Heiko Krude, Amy Lawson‐Yuen, Jan Lebl, M Linder-Lucht, Cláudia Fernandes Lorea, Charles Marques Lourenço, Roelineke J. Lunsing, Greta Lyons, Jana Malíková, Edna E. Mancilla, Anne McGowan, Verónica Mericq, Felipe Monti Lora, Carla Moran, Katalin Eszter Müller, Isabelle Oliver‐Petit, Laura Paone, Praveen George Paul, Michel Polak, Francesco Porta, Fabiano O. Poswar, Christina Reinauer, Klára Roženková, tuba seven menevse, Peter Simm, Anna Simon, Yogen Singh, Marco Spada, Jet van der Spek, Milou A.M. Stals, Athanasia Stoupa, Gopinath M. Subramanian, Davide Tonduti, Serap Turan, Corstiaan A. den Uil, Joel A. Vanderniet, Adri van der Walt, Jean‐Louis Wémeau, Jolante Wierzba, Marie‐Claire Y. de Wit, Nicole I. Wolf, Michael Wurm, Federica Zibordi, Amnon Zung, Nitash Zwaveling‐Soonawala, W. Edward Visser

    प्रकाशित 2020
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    Artigo
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  16. 16
    Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration

    Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration द्वारा Stefan Groeneweg, Ferdy S. van Geest, Mariano Martín, Mafalda Dias, Jonathan Frazer, Carolina Medina‐Gómez, Rosalie Sterenborg, Hao Wang, Anna Dolcetta‐Capuzzo, Linda J. de Rooij, Alexander Teumer, Ayhan Abacı, Erica L T van den Akker, Gautam Ambegaonkar, Christine M. Armour, I. Bacos, Priyanka Bakhtiani, Diana Bârcă, Andrew J. Bauer, Sjoerd A.A. van den Berg, Amanda van den Berge, Enrico Bertini, Ingrid M. van Beynum, Nicola Brunetti‐Pierri, Doris Brunner, Marco Cappa, Gerarda Cappuccio, Barbara Castellotti, Claudia Castiglioni, Krishna Chatterjee, Alexander Chesover, Peter Christian, Jet van der Spek, I.F.M. de Coo, R. Coutant, Dana Craiu, Patricia Crock, Christian de Goede, Korcan Demir, Cheyenne Dewey, Alice Dica, Paul Dimitri, Marjolein H. G. Dremmen, Rachana Dubey, Anina Enderli, Jan Fairchild, Jonathan Gallichan, Luigi Garibaldi, Belinda George, Evelien Gevers, Erin Greenup, Annette Hackenberg, Zita Halász, Bianka Heinrich, Anna Hurst, Tony Huynh, Amber Isaza, Anna Kłosowska, Marieke M van der Knoop, Daniel Konrad, David A. Koolen, Heiko Krude, Abhishek Kulkarni, Alexander Laemmle, Stephen LaFranchi, Amy Lawson‐Yuen, Jan Lebl, Selmar Leeuwenburgh, M Linder-Lucht, Amelia Martí, Cláudia Fernandes Lorea, Charles Marques Lourenço, Roelineke J. Lunsing, Greta Lyons, Jana Malíková, Edna E. Mancilla, Kenneth McCormick, Anne McGowan, Verónica Mericq, Felipe Monti Lora, Carla Moran, Katalin Eszter Müller, Lindsey Nicol, Isabelle Oliver‐Petit, Laura Paone, Praveen George Paul, Michel Polak, Francesco Porta, Fabiano de Oliveira Poswar, Christina Reinauer, Klára Roženková, Rowen Seckold, tuba seven menevse, Peter Simm, Anna Simon, Yogen Singh, Marco Spada, Milou A.M. Stals, Merel T Stegenga, Athanasia Stoupa

    प्रकाशित 2025
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    Artigo
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