检索结果 - Nancy Rodig

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  1. 1
    Growth in children with chronic kidney disease: a report from the Chronic Kidney Disease in Children Study

    Growth in children with chronic kidney disease: a report from the Chronic Kidney Disease in Children Study 由 Nancy Rodig, K. McDermott, Michael F. Schneider, Hilary Hotchkiss, Ora Yadin, Mouin G. Seikaly, Susan L. Furth, Bradley A. Warady

    出版 2014
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  2. 2
    Endothelial expression of PD‐L1 and PD‐L2 down‐regulates CD8<sup>+</sup> T cell activation and cytolysis

    Endothelial expression of PD‐L1 and PD‐L2 down‐regulates CD8<sup>+</sup> T cell activation and cytolysis 由 Nancy Rodig, Timothy A. Ryan, Jessica A. Allen, Hong Pang, Nir Grabie, Tatyana Chernova, Edward Greenfield, Spencer C. Liang, Arlene H. Sharpe, Andrew H. Lichtman, Gordon J. Freeman

    出版 2003
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  3. 3
    Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center

    Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center 由 Weizhen Tan, Svjetlana Lovric, Shazia Ashraf, Jia Rao, David Schapiro, Merlin Airik, Shirlee Shril, Heon Yung Gee, Michelle A. Baum, Ghaleb H. Daouk, Michael A. Ferguson, Nancy Rodig, Michael J.G. Somers, Deborah R. Stein, Asaf Vivante, Jillian K. Warejko, Eugen Widmeier, Friedhelm Hildebrandt

    出版 2017
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  4. 4
    COVID-19 in pediatric kidney transplantation: The Improving Renal Outcomes Collaborative

    COVID-19 in pediatric kidney transplantation: The Improving Renal Outcomes Collaborative 由 Charles D. Varnell, Lyndsay A. Harshman, Laurie Smith, Chunyan Liu, Shiran Chen, Samhar Al‐Akash, Gina-Marie Barletta, Craig W. Belsha, Paul Brakeman, Abanti Chaudhuri, Paul Fadakar, Rouba Garro, Caroline Gluck, Jens Goebel, David Kershaw, Debora Matossian, Corina Nailescu, Hiren P. Patel, Cozumel S. Pruette, Saritha Ranabothu, Nancy Rodig, Jodi M. Smith, Judith Sebestyen VanSickle, Patricia L. Weng, Lara Danziger‐Isakov, David K. Hooper, Michael E. Seifert

    出版 2021
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  5. 5
    Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients

    Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients 由 Nina Mann, Daniela A. Braun, Kassaundra Amann, Weizhen Tan, Shirlee Shril, Dervla M. Connaughton, Makiko Nakayama, Ronen Schneider, Thomas M. Kitzler, Amelie T. van der Ven, Jing Chen, Hadas Ityel, Asaf Vivante, Amar J. Majmundar, Ankana Daga, Jillian K. Warejko, Svjetlana Lovric, Shazia Ashraf, Tilman Jobst‐Schwan, Eugen Widmeier, Hannah Hugo, Shrikant Mane, Leslie Spaneas, Michael J.G. Somers, Michael A. Ferguson, Avram Z. Traum, Deborah R. Stein, Michelle A. Baum, Ghaleb H. Daouk, Richard P. Lifton, Shannon Manzi, Khashayar Vakili, Heung Bae Kim, Nancy Rodig, Friedhelm Hildebrandt

    出版 2019
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  6. 6
    Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

    Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis 由 Ankana Daga, Amar J. Majmundar, Daniela A. Braun, Heon Yung Gee, Jennifer A. Lawson, Shirlee Shril, Tilman Jobst‐Schwan, Asaf Vivante, David Schapiro, Weizhen Tan, Jillian K. Warejko, Eugen Widmeier, Caleb P. Nelson, Hanan Fathy, Zoran Gucev, Neveen A. Soliman, Seema Hashmi, Jan Halbritter, Margarita Halty, Jameela A. Kari, Sherif M. El-Desoky, Michael A. Ferguson, Michael J.G. Somers, Avram Z. Traum, Deborah R. Stein, Ghaleb H. Daouk, Nancy Rodig, A. Katz, Christian Hanna, Andrew L. Schwaderer, John A. Sayer, Ari J. Wassner, Shrikant Mane, Richard P. Lifton, Danko Milošević, Velibor Tasić, Michelle A. Baum, Friedhelm Hildebrandt

    出版 2017
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  7. 7
    Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database

    Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database 由 Matthew Bower, Rémi Salomon, Judith Allanson, Corinne Antignac, Francesco Benedicenti, Elisa Benetti, Gil Binenbaum, Uffe Birk Jensen, Pierre Cochat, Stéphane Decramer, Joanne Dixon, Régen Drouin, Marni J. Falk, Holly Feret, Robert Gise, Alasdair G. W. Hunter, Kisha Johnson, Rajiv Kumar, Marie Pierre Lavocat, Laura Martin, Vincent Morinière, David Mowat, Luisa Murer, Hiep T. Nguyen, Gabriela Peretz‐Amit, Eric A. Pierce, Emily Place, Nancy Rodig, Ann E. Salerno, Sujatha Sastry, Tadashi Sato, John A. Sayer, Gerard C. P. Schaafsma, Lawrence R. Shoemaker, David W. Stockton, Wen‐Hann Tan, Romano Tenconi, Philippe Vanhille, Abhay Vats, Xinjing Wang, Berta Warman, Richard G. Weleber, Susan M. White, Carolyn Wilson-Brackett, Dina J. Zand, Michael R. Eccles, Lisa A. Schimmenti, Laurence Heidet

    出版 2011
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  8. 8
    Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

    Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome 由 Jillian K. Warejko, Weizhen Tan, Ankana Daga, David Schapiro, Jennifer A. Lawson, Shirlee Shril, Svjetlana Lovric, Shazia Ashraf, Jia Rao, Tobias Hermle, Tilman Jobst‐Schwan, Eugen Widmeier, Amar J. Majmundar, Ronen Schneider, Heon Yung Gee, Johanna Magdalena Schmidt, Asaf Vivante, Amelie T. van der Ven, Hadas Ityel, Jing Chen, Carolin E. Sadowski, Stefan Kohl, Werner L. Pabst, Makiko Nakayama, Michael J.G. Somers, Nancy Rodig, Ghaleb H. Daouk, Michelle A. Baum, Deborah R. Stein, Michael A. Ferguson, Avram Z. Traum, Neveen A. Soliman, Jameela A. Kari, Sherif El Desoky, Hanan Fathy, Martin Zenker, Sevcan A. Bakkaloğlu, Dominik Müller, Aytül Noyan, Fatih Özaltın, Melissa A. Cadnapaphornchai, Seema Hashmi, Jeffrey Hopcian, Jeffrey B. Kopp, Nadine Benador, Detlef Böckenhauer, Radovan Bogdanović, Nataša Stajić, Gil Chernin, Robert B. Ettenger, Henry Fehrenbach, Markus J. Kemper, Reyner Loza Munárriz, Ľudmila Podracká, Rainer Büscher, Erkin Serdaroğlu, Velibor Tasić, Shrikant Mane, Richard P. Lifton, Daniela A. Braun, Friedhelm Hildebrandt

    出版 2017
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  9. 9
    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 由 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

    出版 2018
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  10. 10
    Depressive Symptoms in Children with Chronic Kidney Disease

    Depressive Symptoms in Children with Chronic Kidney Disease 由 Amy J. Kogon, Matthew B. Matheson, Joseph T. Flynn, Arlene C. Gerson, Bradley A. Warady, Susan L. Furth, Stephen R. Hooper, Bradley A. Warady, Allison Dart, Larry A. Greenbaum, Bradley A. Warady, Jens Goebel, Mark Mitsnefes, Joseph T. Flynn, Craig S. Wong, Sahar Fathallah, Isidro B. Salusky, Ora Yadin, Katherine M. Dell, Bruce Z. Morgenstern, Tom Blydt‐Hansen, Cynthia G. Pan, Keefe Davis, Amira Al‐Uzri, Randall Jenkins, Anthony A. Portale, Mouin G. Seikaly, Martin A. Turman, Cynthia Wong, Steven R. Alexander, Colleen Hastings, Randall Jenkins, Nancy Rodig, William Harmon, Sharon Bartosh, Nadine Benador, Robert H. Mak, Ellen G. Wood, Randall Jenkins, Gary Lerner, Susan L. Furth, Susan L. Furth, Susan Massengill, Guillermo Sánchez-Archidona Hidalgo, Meredith A. Atkinson, Debbie S. Gipson, Poyyapakkam Srivaths, Joshua Samuels, Frederick J. Kaskel, Debora Mattosian, Yi Cai, Sharon Andreoli, Jeffrey M. Saland, Amy J. Kogon, Victoria F. Norwood, Rulan S. Parekh, Lisa Robinson, Susan R. Mendley, Marc B. Lande, George J. Schwartz, Patrick D. Brophy, Eunice John, Kiran Upadhyay, María Ferris, Tej Matoo, Juan C. Kupferman, Lynne Weiss, Craig B. Langman, Patricia Seo-Mayer, Kanwal K. Kher, D. Samsonov

    出版 2015
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  11. 11
    Estimating Time to ESRD in Children With CKD

    Estimating Time to ESRD in Children With CKD 由 Susan L. Furth, Chris Pierce, Wun Fung Hui, Colin White, Craig S. Wong, Franz Schaefer, Elke Wühl, Alison G. Abraham, Bradley A. Warady, Joshua Samuels, Susan L. Furth, Meredith A. Atkinson, Amy C. Wilson, Alejandro Quiroga, Susan Massengill, Dave Selewski, María Ferris, Amy J. Kogon, Frederick J. Kaskel, Marc B. Lande, George J. Schwartz, Jeffrey M. Saland, Victoria F. Norwood, Tej Matoo, Guillermo Hidalgo, Poyyapakkam Srivaths, Joann Carlson, Craig B. Langman, Susan R. Mendley, Eunice John, Kiran Upadhyay, Patricia Seo-Mayer, Larry T. Patterson, Rulan S. Parekh, Lisa Robinson, Adam Weinstein, Dmitry Samsonov, Juan C. Kupferman, Jason Misurac, Anil Mongia, Steffan Kiessling, Cheryl Sanchez-Kazi, Allison Dart, Sahar Fathallah, Donna Claes, Mark Mitsnefes, Tom Blydt‐Hansen, Bradley A. Warady, Larry A. Greenbaum, Joseph T. Flynn, Craig S. Wong, Isidro B. Salusky, Ora Yadin, Katherine M. Dell, Randall Jenkins, Cynthia G. Pan, Elaine Ku, Amira Al‐Uzri, Randall Jenkins, Nancy Rodig, Cynthia Wong, Keefe Davis, Martin A. Turman, Sharon Bartosh, Colleen Hastings, Anjali Nayak, Mouin G. Seikaly, Nadine Benador, Robert H. Mak, Ellen G. Wood, Randall Jenkins, Gary Lerner, Gina Marie Barletta, Ali Anarat, Ayşı̇n Bakkaloğlu, Fatih Özaltın, Amira Peco‐Antić, Uwe Querfeld, Jutta Gellermann, P. Sallay, Dorota Drożdż, Klaus-Eugen Bonzel, Anne‐Margret Wingen, Aleksandra Żurowska, I Bałasz, Antonella Trivelli, Francesco Perfumo, D. Muller-Wiefel, Kirsten Møller, G. Offner, Barbara Enke, Elke Wühl, Charlotte Hadtstein, Otto Mehls, Franz Schaefer, Sevinç Emre, Salim Çalışkan, S. Mir, Simone Wygoda, Katharina Hohbach-Hohenfellner

    出版 2018
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  12. 12
    Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

    Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations 由 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

    出版 2020
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