Bilaketaren emaitzak - Yalda Jamshidi

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  1. 1
    Characterization of the Human PPARα Promoter: Identification of a Functional Nuclear Receptor Response Element

    Characterization of the Human PPARα Promoter: Identification of a Functional Nuclear Receptor Response Element nork Inès Pineda‐Torra, Yalda Jamshidi, David M. Flavell, Jean‐Charles Fruchart, Bart Staels

    Argitaratua 2002
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  2. 2
    MicroRNA-153 targeting of KCNQ4 contributes to vascular dysfunction in hypertension

    MicroRNA-153 targeting of KCNQ4 contributes to vascular dysfunction in hypertension nork Georgina Carr, Vincenzo Barrese, Jennifer B. Stott, Oleksandr V. Povstyan, Thomas A. Jepps, Hericka B. Figueiredo, Dongling Zheng, Yalda Jamshidi, Iain A. Greenwood

    Argitaratua 2016
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  3. 3
    The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice

    The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice nork Francesca Forzano, Olga Antonova, Angus Clarke, Guido de Wert, Sabine Hentze, Yalda Jamshidi, Yves Moreau, Markus Perola, Inga Prokopenko, Andrew Read, Alexandre Reymond, Vigdís Stefànsdóttir, Carla van El, Maurizio Genuardi, Borut Peterlin, Carla Oliveíra, Karin Writzl, Gunnar Houge, Christophe Cordier, Heidi Howard, Milan Maçek, Béla Melegh, Álvaro Mendes, Dragica Radojković, Emmanuelle Rial‐Sebbag, Fiona Ulph, Yalda Jamshidi

    Argitaratua 2021
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  4. 4
    Variation in the PPARα gene is associated with altered function in vitro and plasma lipid concentrations in Type II diabetic subjects

    Variation in the PPARα gene is associated with altered function in vitro and plasma lipid concentrations in Type II diabetic subjects nork D Flavell, Inès Pineda‐Torra, Yalda Jamshidi, D. Gareth Evans, J. R. Diamond, R. S. Elkeles, Sarah R. Bujac, George Miller, Philippa J. Talmud, Bart Staels, Steve E. Humphries

    Argitaratua 2000
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  5. 5
    Peroxisome Proliferator–Activated Receptor α Gene Regulates Left Ventricular Growth in Response to Exercise and Hypertension

    Peroxisome Proliferator–Activated Receptor α Gene Regulates Left Ventricular Growth in Response to Exercise and Hypertension nork Yalda Jamshidi, Hugh Montgomery, Hans‐Werner Hense, Saul Myerson, Inès Pineda‐Torra, Bart Staels, Michael World, Angela Doering, Jeanette Erdmann, Christian Hengstenberg, Steve E. Humphries, Heribert Schunkert, David M. Flavell

    Argitaratua 2002
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  6. 6
    Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia

    Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia nork Yalda Jamshidi, Ilja M. Nolte, Chrysoula Dalageorgou, Dongling Zheng, Toby Johnson, Rachel Bastiaenen, Suzanne Ruddy, Daniel Talbott, Kris Norris, Harold Snieder, Alfred L. George, Vanessa Marshall, Saad Shakir, Prince J. Kannankeril, Patricia B. Munroe, A. John Camm, Steve Jeffery, Dan M. Roden, Elijah R. Behr

    Argitaratua 2012
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  7. 7
    Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24

    Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24 nork Carola Hedberg‐Oldfors, Alexandra Abramsson, Daniel P. S. Osborn, Olof Danielsson, Afsoon Fazlinezhad, Yalda Nilipour, Laila Hübbert, Inger Nennesmo, Kittichate Visuttijai, Jaipreet Bharj, Evmorfia Petropoulou, Azza Shoreim, Barbara Vona, Najmeh Ahangari, Marcela Dávila López, Mohammad Doosti, Rakesh Kumar Banote, Reza Maroofian, Malin Edling, Mehdi Taherpour, Henrik Zetterberg, Ehsan Ghayoor Karimiani, Anders Oldfors, Yalda Jamshidi

    Argitaratua 2019
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  8. 8
    Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy

    Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy nork Daniel P. S. Osborn, Heather L. Pond, Neda Mazaheri, Jeremy Dejardin, Christopher J. Munn, Khaloob Mushref, Edmund Cauley, Isabella Moroni, Maria Barbara Pasanisi, Elizabeth A. Sellars, Robert Hill, Jennifer N. Partlow, Rebecca Willaert, Jaipreet Bharj, Reza Azizi Malamiri, Hamid Galehdari, Gholamreza Shariati, Reza Maroofian, Marina Mora, Laura E. Swan, Thomas Voit, Francesco J. Conti, Yalda Jamshidi, M. Chiara Manzini

    Argitaratua 2017
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  9. 9
    Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia

    Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia nork Matias Wagner, Daniel P. S. Osborn, Ina Gehweiler, Maike Nagel, Ulrike Ulmer, Somayeh Bakhtiari, Rim Amouri, Reza Boostani, Fayçal Hentati, Maryam M. Hockley, Benedikt V. Hölbling, Thomas Schwarzmayr, Ehsan Ghayoor Karimiani, Christoph Kernstock, Reza Maroofian, Wolfgang Müller‐Felber, Ege Ozkan, Sergio Padilla-López, Selina Reich, Jennifer Reichbauer, Hossein Darvish, Neda Shahmohammadibeni, Abbas Tafakhori, Katharina Vill, Stephan Züchner, Michael C. Kruer, Juliane Winkelmann, Yalda Jamshidi, Rebecca Schüle

    Argitaratua 2019
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  10. 10
    Biallelic <i>SQSTM1</i> mutations in early-onset, variably progressive neurodegeneration

    Biallelic <i>SQSTM1</i> mutations in early-onset, variably progressive neurodegeneration nork Valentina Muto, Elisabetta Flex, Zachary A Kupchinsky, Guido Primiano, Hamid Galehdari, Mohammadreza Dehghani, Serena Cecchetti, Giovanna Carpentieri, Teresa Rizza, Neda Mazaheri, Alireza Sedaghat, Mohammad Yahya Vahidi Mehrjardi, Alice Traversa, Michela Di Nottia, Maria Kousi, Yalda Jamshidi, Andrea Ciolfi, Viviana Caputo, Reza Azizi Malamiri, Francesca Pantaleoni, Simone Martinelli, Aaron R. Jeffries, Jawaher Zeighami, Amir Sherafat, Daniela Di Giuda, Gholamreza Shariati, Rosalba Carrozzo, Nicholas Katsanis, Reza Maroofian, Serenella Servidei, Marco Tartaglia

    Argitaratua 2018
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  11. 11
    Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study

    Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study nork Elijah R. Behr, Eleonora Savio‐Galimberti, Julien Barc, Anders G. Holst, Evmorfia Petropoulou, Bram P. Prins, Javad Jabbari, Margherita Torchio, Myriam Berthet, Yuka Mizusawa, Tao Yang, Eline A. Nannenberg, Federica Dagradi, Peter Weeke, Rachel Bastiaenan, Michael J. Ackerman, Stig Haunsø, Antoine Leenhardt, Stefan Kääb, Vincent Probst, Richard Redon, Sanjay Sharma, Arthur A.M. Wilde, Jacob Tfelt‐Hansen, Peter J. Schwartz, D M Roden, Connie R. Bezzina, Morten S. Olesen, Dawood Darbar, Pascale Guicheney, Lia Crotti, Yalda Jamshidi

    Argitaratua 2015
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  12. 12
    Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes

    Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes nork Elijah R. Behr, Marylyn D. Ritchie, Toshihiro Tanaka, Stefan Kääb, Dana C. Crawford, Paola Nicoletti, Aris Floratos, Moritz F. Sinner, Prince J. Kannankeril, Arthur A.M. Wilde, Connie R. Bezzina, Eric Schulze‐Bahr, Sven Zumhagen, Pascale Guicheney, Nanette H. Bishopric, Vanessa Marshall, Saad Shakir, Chrysoula Dalageorgou, Steve Bevan, Yalda Jamshidi, Rachel Bastiaenen, Robert J. Myerburg, Jean‐Jacques Schott, A. John Camm, Gerhard Steinbeck, Kris Norris, Russ B. Altman, Nicholas P. Tatonetti, Steve Jeffery, Michiaki Kubo, Yusuke Nakamura, Yufeng Shen, Alfred L. George, Dan M. Roden

    Argitaratua 2013
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  13. 13
    Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation: Meta-Analysis of Three Genome-Wide Association Studies

    Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation: Meta-Analysis of Three Genome-Wide Association Studies nork Ilja M. Nolte, Chris Wallace, Stephen Newhouse, Daryl Waggott, Jingyuan Fu, Nicole Soranzo, Rhian Gwilliam, Panos Deloukas, Irina Savelieva, Dongling Zheng, Chrysoula Dalageorgou, Martin Farrall, Nilesh J. Samani, John Connell, Matthew A. Brown, Anna F. Dominiczak, Mark Lathrop, Eleftheria Zeggini, Louise V. Wain, Christopher Newton‐Cheh, Mark Eijgelsheim, Kenneth Rice, Paul I. W. de Bakker, Arne Pfeufer, Serena Sanna, Dan E. Arking, Folkert W. Asselbergs, Tim D. Spector, Nicholas D. Carter, Steve Jeffery, Martin D. Tobin, Mark J. Caulfield, Harold Snieder, Andrew D. Paterson, Patricia B. Munroe, Yalda Jamshidi

    Argitaratua 2009
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  14. 14
    A Large Candidate Gene Survey Identifies the <i>KCNE1</i> D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes

    A Large Candidate Gene Survey Identifies the <i>KCNE1</i> D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes nork Stefan Kääb, Dana C. Crawford, Moritz F. Sinner, Elijah R. Behr, Prince J. Kannankeril, Arthur A.M. Wilde, Connie R. Bezzina, Eric Schulze‐Bahr, Pascale Guicheney, Nanette H. Bishopric, Robert J. Myerburg, Jean‐Jacques Schott, Arne Pfeufer, Britt Maria Beckmann, Eimo Martens, Taifang Zhang, Birgit Stallmeyer, Sven Zumhagen, Isabelle Denjoy, Abdennasser Bardai, Isabelle C. Van Gelder, Yalda Jamshidi, Chrysoula Dalageorgou, Vanessa Marshall, Steve Jeffery, Saad Shakir, A. John Camm, Gerhard Steinbeck, Siegfried Perz, Peter Lichtner, Thomas Meitinger, Annette Peters, H-Erich Wichmann, Christiana D. Ingram, Yuki Bradford, Shannon Carter, Kris Norris, Marylyn D. Ritchie, Alfred L. George, Dan M. Roden

    Argitaratua 2011
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  15. 15
    Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study

    Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study nork Bram P. Prins, Ali Abbasi, Anson Wong, Ahmad Vaez, Ilja M. Nolte, Nora Franceschini, Philip E. Stuart, Javier Guterriez Achury, Vanisha Mistry, Jonathan P. Bradfield, Ana M. Valdes, José Brás, Aleksey Shatunov, Chen Lu, Buhm Han, Soumya Raychaudhuri, Steve Bevan, Maureen D. Mayes, Lam C. Tsoi, Εvangelos Εvangelou, Rajan P. Nair, Struan F.A. Grant, Constantin Polychronakos, Timothy R. D. J. Radstake, David A. van Heel, Melanie Dunstan, Nicholas Wood, Ammar Al‐Chalabi, Abbas Dehghan, Hákon Hákonarson, Hugh S. Markus, James T. Elder, Jo Knight, Dan E. Arking, Timothy D. Spector, Bobby P. C. Koeleman, Cornelia M. van Duijn, Javier Martı́n, Andrew P. Morris, Rinse K. Weersma, Cisca Wijmenga, Patricia B. Munroe, John R. B. Perry, Jennie G. Pouget, Yalda Jamshidi, Harold Snieder, Behrooz Z. Alizadeh

    Argitaratua 2016
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  16. 16
    Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

    Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans nork Daniel S. Evans, Christy L. Avery, Mike A. Nalls, Li Guo, John Barnard, Erin N. Smith, Toshiko Tanaka, Anne M. Butler, Sarah G. Buxbaum, Álvaro Alonso, Dan E. Arking, Gerald S. Berenson, Joshua C. Bis, Steven Buyske, Cara L. Carty, Wei Chen, Mina K. Chung, Steven R. Cummings, Rajat Deo, Charles B. Eaton, Ervin R. Fox, Susan R. Heckbert, Gerardo Heiss, Lucia A. Hindorff, Wen-Chi Hsueh, Aaron Isaacs, Yalda Jamshidi, Kathleen F. Kerr, Felix Liu, Yongmei Liu, Kurt K. Lohman, Jared W. Magnani, Joseph F. Maher, Reena Mehra, Yan Meng, Solomon K. Musani, Christopher Newton‐Cheh, Kari E. North, Bruce M. Psaty, Susan Redline, Jerome I. Rotter, Renate B. Schnabel, Nicholas J. Schork, Ralph V. Shohet, Andrew B. Singleton, Jonathan D. Smith, Elsayed Z. Soliman, Sathanur R. Srinivasan, Herman A. Taylor, David R. Van Wagoner, James G. Wilson, Taylor Young, Zhu-Ming Zhang, Alan B. Zonderman, Michele K. Evans, Luigi Ferrucci, Sarah S. Murray, Gregory J. Tranah, Eric A. Whitsel, Alex P. Reiner, Nona Sotoodehnia

    Argitaratua 2016
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  17. 17
    Biallelic Variants in the Ectonucleotidase <scp><i>ENTPD1</i></scp> Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraplegia

    Biallelic Variants in the Ectonucleotidase <scp><i>ENTPD1</i></scp> Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, a... nork Daniel G. Calame, Isabella Herman, Reza Maroofian, Aren E. Marshall, Karina Carvalho Donis, Jawid M. Fatih, Tadahiro Mitani, Haowei Du, Christopher M. Grochowski, Sérgio B. Sousa, Charul Gijavanekar, Somayeh Bakhtiari, Yoko Itō, Clarissa Rocca, Jill V. Hunter, V. Reid Sutton, Lisa Emrick, Kym M. Boycott, Alexander Lossos, Yakov Fellig, Eugenia Prus, Yosef Kalish, Vardiella Meiner, Manon Suerink, Claudia Ruivenkamp, Kayla Muirhead, Nebal Waill Saadi, Maha S. Zaki, Arjan Bouman, Tahsin Stefan Barakat, David Skidmore, Matthew Osmond, Thiago Oliveira Silva, David Murphy, Ehsan Ghayoor Karimiani, Yalda Jamshidi, Asaad Ghanim Jaddoa, Homa Tajsharghi, Sheng Chih Jin, Mohammad Reza Abbaszadegan, Reza Ebrahimzadeh‐Vesal, Susan Hosseini, Shahryar Alavi, Amir Bahreini, Elahe Zarean, Mohammad Mehdi Salehi, Nouriya Al‐Sannaa, Giovanni Zifarelli, Peter Bauer, Simon C. Robson, Zeynep Coban‐Akdemir, Lorena Travaglini, Francesco Nicita, Shalini N. Jhangiani, Richard A. Gibbs, Jennifer E. Posey, Michael C. Kruer, Kristin D. Kernohan, Jonas Alex Morales Saute, Henry Houlden, Adeline Vanderver, Sarah H. Elsea, Davut Pehli̇van, Dana Marafi, James R. Lupski

    Argitaratua 2022
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  18. 18
    Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

    Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants nork Caroline Neuray, Reza Maroofian, Marcello Scala, Tipu Sultan, G. Shashidhar Pai, Majid Mojarrad, Heba El Khashab, Leigh deHoll, Wyatt W. Yue, Hessa S. Alsaif, M. Natalia Zanetti, Oscar D. Bello, Richard Person, Atieh Eslahi, Zaynab Khazaei, Masoumeh Heidari Feizabadi, Stéphanie Efthymiou, Stanislav Groppa, Blagovesta Marinova Karashova, Wolfgang Nachbauer, Sylvia Boesch, Larissa Arning, Dagmar Timmann, Bru Cormand, Belén Pérez‐Dueñas, Gabriella Di Rosa, Jatinder S. Goraya, Tipu Sultan, Jun Mine, Daniela Avdjieva, Hadil Kathom, Radka Tincheva, Selina Banu, Mercedes Pineda-Marfa, Pierangelo Veggiotti, Michel D. Ferrari, Alberto Verrotti, Gian Luigi Marseglia, Salvatore Savasta, Mayte García-Silva, Alfons Macaya Ruiz, Barbara Garavaglia, Eugenia Borgione, Simona Portaro, Benigno Monteagudo Sanchez, Richard G. Boles, Savvas Papacostas, Michail Vikelis, Eleni Zamba Papanicolaou, Efthimios Dardiotis, Shazia Maqbool, Shahnaz Ibrahim, Salman Kirmani, Nuzhat Rana, Osama Atawneh, Georgios Koutsis, Marianthi Breza, Salvatore Mangano, Carmela Scuderi, Eugenia Borgione, Giovanna Morello, Tanya Stojkovic, Massimi Zollo, Gali Heimer, Yves Dauvilliers, Pasquale Striano, Issam Al-Khawaja, Fuad Al-Mutairi, Sherifa A. Hamed, Hala T. El‐Bassyouni, Doaa Soliman, S. Tekeş, Leyla Özer, Volkan Baltacı, Suliman Khan, Christian Beetz, Khalda Amr, Vincenzo Salpietro, Yalda Jamshidi, Fowzan S. Alkuraya, Henry Houlden

    Argitaratua 2020
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  19. 19
    Genome-wide association analysis identifies multiple loci related to resting heart rate

    Genome-wide association analysis identifies multiple loci related to resting heart rate nork M. Eijgelsheim, Chris Newton-Cheh, N. Sotoodehnia, Paul I. W. de Bakker, Martina Müller‐Nurasyid, Alanna C. Morrison, Albert V. Smith, Aaron Isaacs, Serena Sanna, Marcus Dörr, Pau Navarro, Christian Fuchsberger, I Nolte, Eco J. C. de Geus, Karol Estrada, Shih‐Jen Hwang, Josh Bis, I.-M. Ruckert, Álvaro Alonso, L. J. Launer, J. J. Hottenga, Fernando Rivadeneira, Peter A. Noseworthy, Kenneth Rice, Siegfried Perz, Dan E. Arking, T. D. Spector, Jan A. Kors, Yurii S. Aulchenko, Kirill V. Tarasov, Georg Homuth, SH Wild, Fabio Marroni, Christian Gieger, Carmilla M.M. Licht, Ronald J. Prineas, Albert Hofman, J. I. Rotter, Andrew A. Hicks, Florian Ernst, Samer S. Najjar, A.F. Wright, Annette Peters, Ervin R. Fox, Ben A. Oostra, H K Kroemer, David Couper, Henry Völzke, Harry Campbell, Thomas Meitinger, Manuela Uda, J. C. M. Witteman, Bruce M. Psaty, H-Erich Wichmann, T. B. Harris, Stefan Kääb, David S. Siscovick, Yalda Jamshidi, André G. Uitterlinden, A. R. Folsom, Martin G. Larson, James F. Wilson, Brenda W.J.H. Penninx, Harold Snieder, Peter P. Pramstaller, Cornelia M. van Duijn, Edward G. Lakatta, Stephan B. Felix, Vilmundur Guðnason, Arne Pfeufer, Susan R. Heckbert, Bruno H. Stricker, Eric Boerwinkle, Christopher J. O’Donnell

    Argitaratua 2010
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  20. 20
    Biallelic variants in<i>ARHGAP19</i>cause a motor-predominant neuropathy with asymmetry and conduction slowing

    Biallelic variants in<i>ARHGAP19</i>cause a motor-predominant neuropathy with asymmetry and conduction slowing nork Natalia Dominik, Stéphanie Efthymiou, Christopher J. Record, Xinyu Miao, Reneé C. Lin, Jevin Parmar, Annarita Scardamaglia, Reza Maroofian, Gabriel Aughey, Abigail D. Wilson, Simon A. Lowe, Riccardo Currò, Ricardo Parolin Schnekenberg, Shahryar Alavi, Leif Leclaire, Yi He, Kristina Zhelchenska, Yohanns Bellaı̈che, Isabelle Gaugué, Mariola Skorupinska, Liedewei Van de Vondel, Sahar I. Da’as, Valentina Turchetti, Serdal Güngör, Ehsan Ghayoor Karimiani, Camila Armirola-Ricaurte, Haluk Topaloğlu, Albena Jordanova, Mashaya Zaman, Selina Banu, Wilson Marques, Pedro José Tomaselli, Büşra Aynekin, Ali Cansu, Hüseyin Per, Ayten Güleç, Javeria Raza Alvi, Tipu Sultan, Arif Khan, Giovanni Zifarelli, Shahnaz Ibrahim, Grazia M.S. Mancini, M. Mahdi Motazacker, Esther Brusse, Vincenzo Lupo, Teresa Sevilla, A. Nazlı Başak, Şeyma Tekgül, Robin Palvadeau, Jonathan Baets, Yeşim Parman, Arman Çakar, Rita Horváth, Tobias B. Haack, J. Stahl, Kathrin Grundmann‐Hauser, Joohyun Park, Stephan Züchner, Nigel G. Laing, Lindsay Wilson, Alexander M. Rossor, James M. Polke, Fernanda Barbosa Figueiredo, André Luiz Santos Pessoa, Fernando Kok, Antônio Rodrigues Coimbra Neto, Marcondes C. França, Yalda Jamshidi, Gianina Ravenscroft, Sherifa A. Hamed, Wendy K. Chung, Daniel P. S. Osborn, Michael G. Hanna, Andrea Cortese, Mary M. Reilly, James E.C. Jepson, Nathalie Lamarche‐Vane, Henry Houlden

    Argitaratua 2024
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