نتائج البحث - "Potratz, Cornelia"

1

دورية أكاديمية

Platform trial design for neurofibromatosis type 1, NF2-related schwannomatosis and non-NF2-related schwannomatosis:A potential model for rare diseases

المصدر: Dhaenens , B A E , Heimann , G , Bakker , A , Nievo , M , Ferner , R E , Evans , D G , Wolkenstein , P , Leubner , J , Potratz , C , Carton , C , Iloeje , U , Kirk , G , Blakeley , J O , Plotkin , S , Fisher , M J , Kim , A , Driever , P H , Azizi , A A , Widemann , B C , Gross , A , Parke , T , Legius , E & Oostenbrink , ....

وصف الملف: application/pdf

العلاقة: https://pure.eur.nl/en/publications/d4a21425-c0df-4db6-ae17-09111a025a04Test

الإتاحة: https://doi.org/10.1093/nop/npae001Test
https://pure.eur.nl/en/publications/d4a21425-c0df-4db6-ae17-09111a025a04Test
https://pure.eur.nl/ws/files/135612928/npae001.pdfTest
https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=eur_pure&SrcAuth=WosAPI&KeyUT=WOS:001152283100001&DestLinkType=FullRecord&DestApp=WOSTest

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2

دورية أكاديمية

Current state-of-the-art and gaps in platform trials: 10 things you should know, insights from EU-PEARL

المؤلفون: Koenig, Franz, Spiertz, Cécile, Millar, Daniel, Rodríguez-Navarro, Sarai, Machín, Núria, Van Dessel, Ann, Genescà, Joan, Pericàs, Juan M., Posch, Martin, Sánchez-Montalva, Adrian, Estevez, Ana Belén, Sánchez, Àlex, Sanjuan, Anna, Sena, Elena, Granados, Emma, Arévalo de Andrés, Esther, Nuñez, Fátima, Arteaga, Gara, Fuentes Ruiz, Gabriela Perez, Fernández, Guillermo, Rivera-Esteban, Jesus, Comella, Joan, Ramos-Quiroga, Josep Antoni, Espinosa, Juan, Pericàs, Juan Manuel, Murcia, Lada, Cash-Gibson, Lucinda, de Valles Silvosa, Maria, Barroso de Sousa, María Fernanda, Sánchez-Maroto Carrizo, Olga, Ibañez-Jiménez, Pol, Augustin, Salvador, Perez-Hoyos, Santiago, Muñoz-Martínez, Sergio, Serres, Silvia, Kalko, Susana, Michon, Amelie, Ussi, Anton, Lydall, Ben, van de Ketterij, Edwin, Quiles, Ignacio, Carapina, Tamara, Kumaus, Constantin, Ramazanova, Dariga, Meyer, Elias Laurin, Roig, Marta Bofill, Brunner, Martin, Krotka, Pavla, Zehetmayer, Sonja, Carton, Charlotte, Legius, Eric, Begum, Amina, Pariante, Carmine, Worrell, Courtney, Lombardo, Giulia, Sforzini, Luca, Brown, Mollie, Gullet, Nancy, Amasi-Hartoonian, Nare, Ferner, Rosalie, Kose, Melisa, Spitaleri, Andrea, Ghodousi, Arash, Di Serio, Clelia, Cirillo, Daniela, Cugnata, Federica, Saluzzo, Francesca, Benedetti, Francesco, Scarale, Maria Giovanna, Zini, Michela, Rancoita, Paola Maria, Alagna, Riccardo, Poletti, Sara, Dhaenens, Britt, Van Der Lei, Johan, de Steenwinkel, Jurriaan, Moinat, Maxim, Oostenbrink, Rianne, Hoogendijk, Witte, Hölscher, Michael, Heinrich, Norbert, Otte, Christian, Potratz, Cornelia, Zocholl, Dario, Kulakova, Eugenia, Tacke, Frank, Brasanac, Jelena, Leubner, Jonas, Krajewska, Maja, Freitag, Michaela Maria, Gold, Stefan, Zoller, Thomas, Chae, Woo Ri, Daniel, Christel, Kara, Leila, Vaterkowski, Morgan, Griffon, Nicolas, Wolkenstein, Pierre, Pais, Raluca, Ratziu, Vlad, Voets, David, Maes, Christophe, Kalra, Dipak, Thienpoint, Geert, Deckerck, Jens, Lea, Nathan, Singleton, Peter, Viele, Kert, Jacko, Peter, Berry, Scott, Parke, Tom, Aydin, Burç, Kubiak, Christine, Demotes, Jacques, Ueda, Keiko, Matei, Mihaela, Contrino, Sergio, Röhl, Claas, Cordero, Estefania, Greenhalgh, Fiona, Jarke, Hannes, Angelova, Juliana, Boudes, Mathieu, Dressler, Stephan, Strammiello, Valentina, Anstee, Quentin, Gutierrez-Ibarluzea, Iñaki, Otte, Maximilian, Heimbach, Natalie, Hofner, Benjamin, Burgwinkel, Cora, Kaestel, Hue, Hees, Katharina, Nguyen, Quynh, Prieto-Alhambra, Daniel, Tan, Eng Hooi (Cheryl), Raviglione, Mario, de Colombani, Pierpaolo, Villa, Simone, Maron, Eduard, Evans, Gareth, Savitz, Adam J., Duca, Anna, Kaminski, Anne, Wouters, Bie, Porter, Brandon, Charron, Catherine, Spiertz, Cecile, Zizzamia, Christopher, Hasselbaink, Danny, Orr, David, Kesters, Divya, Hubin, Ellen, Davies, Emma, Didden, Eva-Maria, Guz, Gabriela, Verstraete, Evelyn, Mao, Gary, Capuano, George, Martynowicz, Heddie, De Smedt, Heidi, Larsson, Ingela, Bruegelmans, Ines, Coste, Isabelle, Gonzalez Moreno, Jesus Maria, Niewczas, Julia, Xu, Jiajun, Rombouts, Karin, Woo, Katherine, Wuyts, Kathleen, Hersh, Kathryn, Oldenburg, Khrista, Zhang, Lingjiao, Schmidt, Mark, Szuch, Mark, Todorovic, Marija, Mangelaars, Maartje, Grewal, Melissa, Sandor, Molli, Di Prospero, Nick, Van Houten, Pamela, Minnick, Pansy, Bastos, Polyana, Patrizi, Robert, Morello, Salvatore, De Wilde, Severijn, Sun, Tao, Kline, Timothy, de Marez, Tine, Mielke, Tobias, Reijns, Tom, Popova, Vanina, Flossbach, Yanina, Tymofyeyev, Yevgen, De Groote, Zeger, Sverdlov, Alex, Bobirca, Alexandra, Krause, Annekatrin, Bobrica, Catalin, Heintz, Daniela, Magirr, Dominic, Glimm, Ekkehard, Baffert, Fabienne, Castiglione, Federica, Caruso, Franca, Patalano, Francesco, Bretz, Frank, Heimann, Guenter, Carbarns, Ian, Rodríguez, Ignacio, Ratescu, Ioana, Hampson, Lisa, Pedrosa, Marcos, Hark, Mareile, Mesenbrink, Peter, Penna, Sabina Hernandez, Bergues-Lang, Sarah, Baltes-Engler, Susanne, Arsiwala, Tasneem, Mondragon, Valeria Jordan, Guo, Hua, Da Costa, Jose Leite, Burman, Carl-Fredrik, Kirk, George, Aaes-Jørgensen, Anders, Dirach, Jorgen, Kjær, Mette Skalshøi, Martin, Alexandra, Hristov, Diyan, Rousseaux, Florent, Hittel, Norbert, Dornheim, Robert, Evans, Daniel, Sykes, Nick, Couvert, Camille, Leuven, Catherine, Notelet, Loïc, Gidh-Jain, Madhavi, Jouannin, Mathieu, Ammour, Nadir, Pierre, Suzanne, Haufe, Volker, Dong, Yingwen, Dubanchet, Catherine, de Préville, Nathalie, Baltauss, Tania, Jian, Zhu, Shnider, Sara, Bar-El, Tal, Bakker, Annette, Nievo, Marco, Iloeje, Uche, Conradie, Almari, Auffarrth, Ece, Lombard, Leandra, Benhayoun, Majda, Olugbosi, Morounfolu, Seidel, Stephanie S., Gumí, Berta, Guzmán, Claudia García, Molero, Eva, Pairó, Gisela, Machin, Núria, Cardelús, Raimon, Ramasastry, Saira, Pelzer, Saskia, Kremer, Andreas, Lindfors, Erno, Lynch, Chris

المساهمون: F. Koenig, C. Spiertz, D. Millar, S. Rodríguez-Navarro, N. Machín, A. Van Dessel, J. Genescà, J.M. Pericà, M. Posch, A. Sánchez-Montalva, A.B. Estevez, À. Sánchez, A. Sanjuan, E. Sena, E. Granado, E. Arévalo de André, F. Nuñez, G. Arteaga, G.P. Fuentes Ruiz, G. Fernández, J. Rivera-Esteban, J. Comella, J.A. Ramos-Quiroga, J. Espinosa, L. Murcia, L. Cash-Gibson, M. de Valles Silvosa, M.F. Barroso de Sousa, O. Sánchez-Maroto Carrizo, P. Ibañez-Jiménez, S. Augustin, S. Perez-Hoyo, S. Muñoz-Martínez, S. Serre, S. Kalko, A. Michon, A. Ussi, B. Lydall, E. van de Ketterij, I. Quile, T. Carapina, C. Kumau, D. Ramazanova, E.L. Meyer, M.B. Roig, M. Brunner, P. Krotka, S. Zehetmayer, C. Carton, E. Legiu, A. Begum, C. Pariante, C. Worrell, G. Lombardo, L. Sforzini, M. Brown, N. Gullet, N. Amasi-Hartoonian, R. Ferner, M. Kose, A. Spitaleri, A. Ghodousi, C. Di Serio, D. Cirillo, F. Cugnata, F. Saluzzo, F. Benedetti, M.G. Scarale, M. Zini, P.M. Rancoita, R. Alagna, S. Poletti, B. Dhaenen, J. Van Der Lei, J. de Steenwinkel, M. Moinat, R. Oostenbrink, W. Hoogendijk, M. Hölscher, N. Heinrich, C. Otte, C. Potratz, D. Zocholl, E. Kulakova, F. Tacke, J. Brasanac, J. Leubner, M. Krajewska, M.M. Freitag, S. Gold, T. Zoller, W.R. Chae, C. Daniel, L. Kara, M. Vaterkowski

مصطلحات موضوعية: Adaptive design, Clinical research, Integrated research platform, Master protocol, Patient-centred, Settore BIO/10 - Biochimica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/38226342; info:eu-repo/semantics/altIdentifier/wos/WOS:001149726400001; volume:67; firstpage:1; lastpage:12; numberofpages:12; journal:ECLINICALMEDICINE; https://hdl.handle.net/2434/1041651Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85180956599

الإتاحة: https://doi.org/10.1016/j.eclinm.2023.102384Test
https://hdl.handle.net/2434/1041651Test

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3

Case report: KPTN gene-related syndrome associated with a spectrum of neurodevelopmental anomalies including severe epilepsy

المؤلفون: Horn, Svea, Danyel, Magdalena, Erdmann, Nina, Boschann, Felix, Gunnarsson, Cecilia, 1970, Biskup, Saskia, Juengling, Jerome, Potratz, Cornelia, Prager, Christine, Kaindl, Angela M.

المصدر: Frontiers in Neurology. 13

مصطلحات موضوعية: KPTN gene, macrocephaly, neurodevelopment delay, epilepsy, splice site variant

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-191744Test
https://liu.diva-portal.org/smash/get/diva2:1736334/FULLTEXT01.pdfTest

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4

دورية أكاديمية

Tumor load rather than contrast enhancement is associated with the visual function of children and adolescents with optic pathway glioma – a retrospective Magnetic Resonance Imaging study

المؤلفون: Kilian, Anna, Aigner, Annette, Simon, Michèle, Salchow, Daniel J., Potratz, Cornelia, Thomale, Ulrich-Wilhelm, Hernáiz Driever, Pablo, Tietze, Anna

المساهمون: Deutsche Forschungsgemeinschaft, Charité - Universitätsmedizin Berlin

المصدر: Journal of Neuro-Oncology ; volume 156, issue 3, page 589-597 ; ISSN 0167-594X 1573-7373

مصطلحات موضوعية: Cancer Research, Neurology (clinical), Neurology, Oncology

الإتاحة: https://doi.org/10.1007/s11060-021-03941-1Test

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5

دورية أكاديمية

Identifying challenges in neurofibromatosis:a modified Delphi procedure

المؤلفون: Dhaenens, Britt A.E., Ferner, Rosalie E., Bakker, Annette, Nievo, Marco, Evans, D. Gareth, Wolkenstein, Pierre, Potratz, Cornelia, Plotkin, Scott R., Heimann, Guenter, Legius, Eric, Oostenbrink, Rianne

المصدر: Dhaenens , B A E , Ferner , R E , Bakker , A , Nievo , M , Evans , D G , Wolkenstein , P , Potratz , C , Plotkin , S R , Heimann , G , Legius , E & Oostenbrink , R 2021 , ' Identifying challenges in neurofibromatosis : a modified Delphi procedure ' , European Journal of Human Genetics , vol. 29 , no. 11 , pp. 1625-1633 . https://doi.org/10.1038/s41431-021-00892-zTest

وصف الملف: application/pdf

الإتاحة: https://doi.org/10.1038/s41431-021-00892-zTest
https://pure.eur.nl/en/publications/47e286f4-3a75-40a8-9b73-afb95b9a2e7cTest
https://pure.eur.nl/ws/files/43471342/Identifying_challenges_in_neurofibromatosis_a_modified_Delphi_procedure.pdfTest
http://www.scopus.com/inward/record.url?scp=85105193839&partnerID=8YFLogxKTest

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6

دورية أكاديمية

Lessons learned from drug trials in neurofibromatosis:A systematic review

المؤلفون: Dhaenens, Britt A.E., Ferner, Rosalie E., Evans, D. Gareth, Heimann, Guenter, Potratz, Cornelia, van de Ketterij, Edwin, Kaindl, Angela M., Hissink, Geesje, Carton, Charlotte, Bakker, Annette, Nievo, Marco, Legius, Eric, Oostenbrink, Rianne

المصدر: Dhaenens , B A E , Ferner , R E , Evans , D G , Heimann , G , Potratz , C , van de Ketterij , E , Kaindl , A M , Hissink , G , Carton , C , Bakker , A , Nievo , M , Legius , E & Oostenbrink , R 2021 , ' Lessons learned from drug trials in neurofibromatosis : A systematic review ' , European Journal of Medical Genetics , vol. 64 , no. 9 , 104281 . https://doi.org/10.1016/j.ejmg.2021.104281Test

الإتاحة: https://doi.org/10.1016/j.ejmg.2021.104281Test
https://pure.eur.nl/en/publications/8118ce3b-c70d-4b0b-b224-20b4e97efc4fTest
http://www.scopus.com/inward/record.url?scp=85110104876&partnerID=8YFLogxKTest

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