نتائج البحث - Loai Eid

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  1. 1
    Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract

    Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract حسب Amelie T. van der Ven, Dervla M. Connaughton, Hadas Ityel, Nina Mann, Makiko Nakayama, Jing Chen, Asaf Vivante, Daw‐Yang Hwang, Julian Schulz, Daniela A. Braun, Johanna Magdalena Schmidt, David Schapiro, Ronen Schneider, Jillian K. Warejko, Ankana Daga, Amar J. Majmundar, Weizhen Tan, Tilman Jobst‐Schwan, Tobias Hermle, Eugen Widmeier, Shazia Ashraf, Ali Amar, Charlotte A. Hoogstraaten, Hannah Hugo, Thomas M. Kitzler, Franziska Kause, Caroline M. Kolvenbach, Rufeng Dai, Leslie Spaneas, Kassaundra Amann, Deborah R. Stein, Michelle A. Baum, Michael J.G. Somers, Nancy Rodig, Michael A. Ferguson, Avram Z. Traum, Ghaleb H. Daouk, Radovan Bogdanović, Nataša Stajić, Neveen A. Soliman, Jameela A. Kari, Sherif El Desoky, Hanan Fathy, Danko Milošević, Muna Al‐Saffar, Hazem S. Awad, Loai Eid, Aravind Selvin, Prabha Senguttuvan, Simone Sanna‐Cherchi, Heidi L. Rehm, Daniel G. MacArthur, Monkol Lek, Kristen M. Laricchia, Michael W. Wilson, Shrikant Mane, Richard P. Lifton, Richard S. Lee, Stuart B. Bauer, Lu W, Heiko Reutter, Velibor Tasić, Shirlee Shril, Friedhelm Hildebrandt

    منشور في 2018
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  2. 2
    Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease

    Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease حسب Kathrin Burgmaier, Kevin Kunzmann, Gema Ariceta, Carsten Bergmann, Anja Buescher, Mathias Burgmaier, İsmail Dursun, Ali Düzova, Loai Eid, Florian Erger, Markus Feldkoetter, Matthias Galiano, Michaela Geßner, Heike Goebel, İbrahim Gökçe, Dieter Haffner, Nakysa Hooman, Bernd Höppe, Augustina Jankauskiené, Günter Klaus, Jens König, Mieczysław Litwin, Laura Massella, Djalila Mekahli, Engin Melek, Sevgı Mır, Lars Pape, Larisa Prikhodina, Bruno Ranchin, Raphael Schild, Tomáš Seeman, Lale Sever, Rukshana Shroff, Neveen A. Soliman, Stella Stabouli, Małgorzata Stańczyk, Yılmaz Tabel, Katarzyna Taranta‐Janusz, Sara Testa, Julia Thumfart, Rezan Topaloĝlu, Lutz T. Weber, Dorota Wicher, Elke Wühl, Simone Wygoda, Alev Yılmaz, Katarzyna Zachwieja, Ilona Zagożdżon, Klaus Zerres, Jörg Dötsch, Franz Schaefer, Max C. Liebau, Nadejda Ranguelov, Nathalie Godefroid, Laure Collard, Jacques Lombet, Julie Maquet, Gesa Schalk, Uwe Querfeld, Bodo B. Beck, Thomas Benzing, Reinhard Buettner, Franziska Grundmann, Christine Kurschat, Kerstin Benz, Anja Tzschoppe, Bjoern Buchholz, Rainer Buescher, Karsten Häffner, Martin Pöhl, Oliver Groß, Jenny Krügel, Johanna Stock, Ludwig Patzer, Jun Oh, Wanja M. Bernhardt, Anke Doyon, Tobias Vinke, Anja Sander, Michael Henn, Ute Derichs, Rolf Beetz, Nikola Jeck, Bärbel Lange-Sperandio, Sabine Ponsel, Franziska Kusser, Barbara Uetz, Marcus R. Benz, Silke Schmidt, C. J. Huppertz-Kessler, Birgitta Kranz, Andrea Titieni, Donald Wurm, Heinz E. Leichter, Martin Bald, Heiko Billing, Marwa M. Nabhan, Luis Enrique Lara, Fotiοs Papachristou, Francesco Emma

    منشور في 2018
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  3. 3
    Global Variation of Nutritional Status in Children Undergoing Chronic Peritoneal Dialysis: A Longitudinal Study of the International Pediatric Peritoneal Dialysis Network

    Global Variation of Nutritional Status in Children Undergoing Chronic Peritoneal Dialysis: A Longitudinal Study of the International Pediatric Peritoneal Dialysis Network حسب Franz Schaefer, Laura Benner, Dagmara Borzych–Dużałka, Joshua J. Zaritsky, Hong Xu, Lesley Rees, Zenaida L. Antonio, Erkin Serdaroğlu, Nakysa Hooman, Hiren P. Patel, Lale Sever, Karel Vondrák, Joseph T. Flynn, Anabella Rébori, William Wong, Tuula Hölttä, Zeynep Yürük Yıldırım, Bruno Ranchin, Ryszard Grenda, Sara Testa, Dorota Drożdż, Attila J. Szabó, Loai Eid, Biswanath Basu, Renata Vitkevič, Cynthia Wong, Stephen J. Pottoore, Dominik N. Müller, Ruhan Düşünsel, Claudia González, Marc Fila, Lisa Sartz, Anja Sander, Bradley A. Warady, M Adragna, Paula A. Coccia, Ángela Suárez, Patricia G. Vallés, Reza Salim, Laura Alconcher, Klaus Arbeiter, K. van Hoeck, Vera Hermina Kalika Koch, Janusz Feber, Elizabeth Harvey, Colin White, M. Valenzuela, Jorge Villagrá, F. Cano, M Contreras, A. Vogel, Pedro Sepúlveda Zambrano, P Hevia, Mc Chiu, Jie Ding, Juan José Vanegas, Lina María Serna‐Higuita, G. Roussey, Tim Ulinski, Saoussen Krid, Michel Fischbach, Jérôme Harambat, Ch. Samaille, Rainer Büscher, Jun Oh, Lars Pape, Ulrich John, Günter Klaus, H. Billing, C. Stafanidis, Fotiοs Papachristou, Arvind Bagga, Madhuri Kanitkar, Rajiv Sinha, Sanjum S. Sethi, Enrico Verrina, Enrico Vidal, Giovanna Leozappa, Daniel Landau, Il Soo Ha, Kyu-hyun Paik, Ahmad Bilal, E Sahpazova, Yam-Ngo Lim, Lorena Sànchez Barbosa, Jaap W. Groothoff, Y. Konijenberg, Yolanda Silva, M. Al Ryami, Reyner Loza Munárriz, Bożena Leszczyńska, Maria Szczepańska, O Brumariu, Jameela A. Kari, D Kruscić, Hui‐Kim Yap, Gema Ariceta, Mireia Aguirre, Fernando Santos, Bogna Niwinska-Faryna

    منشور في 2019
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  4. 4
    ADPedKD: A Global Online Platform on the Management of Children With ADPKD

    ADPedKD: A Global Online Platform on the Management of Children With ADPKD حسب Stéphanie De Rechter, Detlef Böckenhauer, Lisa M. Guay‐Woodford, Isaac Liu, Andrew Mallett, Neveen A. Soliman, Lucimary C. Sylvestre, Franz Schaefer, Max C. Liebau, Djalila Mekahli, Piotr Adamczyk, Nurver Akıncı, Harika Alpay, Carmen Ardelean, Nadia Ayasreh, Zeki Aydın, A. Bael, Véronique Baudouin, US Bayrakci, A Bensman, Hanna Bialkevich, A. Biebuyck, Olivia Boyer, Omar Bjanid, Olivia Boyer, A. Bryłka, Salim Çalışkan, Alexandra Cambier, A. Camelio, Vincenza Carbone, Marina Charbit, Benedetta Chiodini, A. Chirita, Neslihan Çiçek, Rimantė Čerkauskienė, Laure Collard, Magda S. da Conceição, Ileana Constantinescu, Anne‐Laure Couderc, B. Crapella, Mirjana Cvetković, B. Dima, F. Diomeda, M. Docx, Nancy C. Dolan, Claire Dossier, Dorota Drożdż, Jens Drube, Oliver Dunand, Dušan Paripović, Loai Eid, Francesco Emma, M. Espino Hernández, Marc Fila, Mónica Furlano, Mihai Gafencu, M.S. Ghuysen, Mauro Giani, Mario Giordano, I. Girisgen, Nathalie Godefroid, Astrid Godron-Dubrasquet, I. Gojkovic, Elizabeth M. Gonzalez, İbrahim Gökçe, Jaap W. Groothoff, Stefano Guarino, Anne Guffens, P. R. Hansen, Jérôme Harambat, Sara Kretzschmar Haumann, Guanheng He, Laurence Heidet, Remon Helmy, F. Hémery, Nakysa Hooman, Brigitte Llanas, Augustina Jankauskiené, Peter Janssens, S. Karamaria, I. A. Kazyra, Julian Koenig, Saoussen Krid, Penny Krug, V. Kwon, Angela La Manna, V. Leroy, Mieczysław Litwin, Jacques Lombet, Germana Longo, Adrian Lungu, Amali Mallawaarachchi, Anna Marín, P. Marzuillo, Laura Massella, Antonio Mastrangelo, Helen McCarthy, Monika Miklaszewska, Anna Moczulska, Giovanni Montini

    منشور في 2019
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  5. 5
    Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants

    Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants حسب Kathrin Burgmaier, Leonie Violetta Brinker, Florian Erger, Bodo B. Beck, Marcus R. Benz, Carsten Bergmann, Olivia Boyer, Laure Collard, Claudia Dafinger, Marc Fila, Claudia Kowalewska, Bärbel Lange-Sperandio, Laura Massella, Antonio Mastrangelo, Djalila Mekahli, Monika Miklaszewska, Nadina Ortiz-Bruechle, Ludwig Patzer, Larisa Prikhodina, Bruno Ranchin, Nadejda Ranguelov, Raphael Schild, Tomáš Seeman, Lale Sever, Przemysław Sikora, Maria Szczepańska, Ana Teixeira, Julia Thumfart, Barbara Uetz, Lutz T. Weber, Elke Wühl, Klaus Zerres, Jörg Dötsch, Franz Schaefer, Max C. Liebau, Loai Eid, Klaus Arbeiter, Nathalie Godefroid, Jacques Lombet, Aurélie De Mul, Markus Feldkoetter, Jakub Zieg, Franziska Grundmann, Matthias Galiano, Bjoern Buchholz, Anja Buescher, Karsten Häffner, Oliver Groß, Ludwig Patzer, Jun Oh, Dieter Haffner, Wanja M. Bernhardt, Susanne Schaefer, Simone Wygoda, Jan Halbritter, Ute Derichs, Günter Klaus, Felix Lechner, Sabine Ponsel, Jens König, Hagen Staude, Donald Wurm, Martin Bald, Michaela Geßner, Neveen A. Soliman, Gema Ariceta, Juan David González-Rodríguez, Francisco de la Cerda Ojeda, Jérôme Harambat, Denis Morin, Claire Dossier, Guillaume Dorval, Rukshana Shroff, Stella Stabouli, Nakysa Hooman, Francesca Mencarelli, William Morello, Germana Longo, Francesco Emma, Augustina Jankauskiené, Katarzyna Taranta‐Janusz, Ilona Zagożdżon, Katarzyna Zachwieja, Małgorzata Stańczyk, Beata Bieniaś, Mieczysław Litwin, Aurelia Morawiec‐Knysak, Alberto Caldas Afonso, Oliver Dunand, Andreea Liana Răchişan, Gordana Miloševski‐Lomić, Svetlana Papizh, Rina Rus, Houweyda Jilani, Bahriye Atmış, Ali Düzova, Alper Soylu, Cengiz Candan, Salim Çalışkan, Alev Yılmaz

    منشور في 2021
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  6. 6
    Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

    Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations حسب Dervla M. Connaughton, Rufeng Dai, Danielle Owen, Jonathan Marquez, Nina Mann, Adda L. Graham-Paquin, Makiko Nakayama, Étienne Coyaud, Estelle Laurent, Jonathan St‐Germain, Lot Snijders Blok, Arianna Vino, Verena Klämbt, Konstantin Deutsch, Chen-Han Wilfred Wu, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Ronen Schneider, Thomas M. Kitzler, Amar J. Majmundar, Florian Buerger, Ana C. Onuchic-Whitford, Youying Mao, Amy Kolb, Daanya Salmanullah, Evan Chen, Amelie T. van der Ven, Jia Rao, Hadas Ityel, Steve Seltzsam, Johanna M. Rieke, Jing Chen, Asaf Vivante, Daw‐Yang Hwang, Stefan Kohl, Gabriel C. Dworschak, Tobias Hermle, Mariëlle Alders, Tobias Bartolomaeus, Stuart B. Bauer, Michelle A. Baum, Eva H. Brilstra, Thomas D. Challman, Jacob Zyskind, Carrie E. Costin, Katrina M. Dipple, Floor A.M. Duijkers, Marcia Ferguson, David Fitzpatrick, Roger Fick, Ian Glass, Peter J. Hulick, Antonie D. Kline, Ilona Krey, Selvin Kumar, Lu W, Elysa J. Marco, Ingrid M. Wentzensen, Heather C. Mefford, Konrad Platzer, Inna Povolotskaya, Juliann M. Savatt, Н. В. Щербакова, Prabha Senguttuvan, Audrey Squire, Deborah R. Stein, Isabelle Thiffault, V. Yu. Voinova, Michael J. Somers, Michael A. Ferguson, Avram Z. Traum, Ghaleb H. Daouk, Ankana Daga, Nancy Rodig, Paulien A. Terhal, Ellen van Binsbergen, Loai Eid, Velibor Tasić, Hila Milo Rasouly, Tze Y. Lim, Dina Ahram, Ali G. Gharavi, Heiko Reutter, Heidi L. Rehm, Daniel G. MacArthur, Monkol Lek, Kristen M. Laricchia, Richard P. Lifton, Hong Xu, Shrikant Mane, Simone Sanna‐Cherchi, Andrew D. Sharrocks, Brian Raught, Simon E. Fisher, Maxime Bouchard, Mustafa K. Khokha, Shirlee Shril, Friedhelm Hildebrandt

    منشور في 2020
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