Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management von Bierzynska, Agnieszka, McCarthy, Hugh J., Soderquest, Katrina, Sen, Ethan S., Colby, Elizabeth, Ding, Wen Y., Nabhan, Marwa M., Kerecuk, Larissa, Hegde, Shivram, Hughes, David, Marks, Stephen, Feather, Sally, Jones, Caroline, Webb, Nicholas J.A., Ognjanovic, Milos, Christian, Martin, Gilbert, Rodney D., Sinha, Manish D., Lord, Graham M., Simpson, Michael, Koziell, Ania B., Welsh, Gavin I., Saleem, Moin A.

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Clinical and molecular characterization of primary hyperoxaluria in Egypt von Soliman, Neveen A., Elmonem, Mohamed A., Abdelrahman, Safaa M., Nabhan, Marwa M., Fahmy, Yosra A., Cogal, Andrea, Harris, Peter C., Milliner, Dawn S.

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Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies von Schueler, Markus, Halbritter, Jan, Phelps, Ian G, Braun, Daniela A, Otto, Edgar A, Porath, Jonathan D, Gee, Heon Yung, Shendure, Jay, O'Roak, Brian J, Lawson, Jennifer A, Nabhan, Marwa M, Soliman, Neveen A, Doherty, Dan, Hildebrandt, Friedhelm

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Clinical characterization and nphp1 mutations in nephronophthisis and associated ciliopathies : a single center experience von al-Kiki, Hassan, Jawdat, Ghadah, Fiddah, Sawsan, Shiba, Maha, Badr, Ahmad, Allen, Susan J., Nabhan, Marwah M., Otto, Edgar A., Hildebrandt, Friedhelm, Sulayman, Nifin A.

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Cystic kidneys in fetal Walker–Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literature von Nabhan, Marwa M., ElKhateeb, Nour, Braun, Daniela A., Eun, Sungho, Saleem, Sahar N., YungGee, Heon, Hildebrandt, Friedhelm, Soliman, Neveen A.

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Combined liver‐kidney transplantation for primary hyperoxaluria type I in children: Single Center Experience von Kotb, Magd A., Hamza, Alaa F., Abd El Kader, Hesham, El Monayeri, Magda, Mosallam, Dalia S., Ali, Nazira, Basanti, Christine William Shaker, Bazaraa, Hafez, Abdelrahman, Hany, Nabhan, Marwa M., Abd El Baky, Hend, El Sorogy, Sally T. Mostafa, Kamel, Inas E.M., Ismail, Hoda, Ramadan, Yasmin, Abd El Rahman, Safaa M., Soliman, Neveen A.

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Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome von Schneider, Ronen, Shril, Shirlee, Buerger, Florian, Deutsch, Konstantin, Yousef, Kirollos, Frank, Camille N., Onuchic-Whitford, Ana C., Kitzler, Thomas M., Mao, Youying, Klämbt, Verena, Zahoor, Muhammad Y., Lemberg, Katharina, Majmundar, Amar J., Mansour, Bshara, Saida, Ken, Seltzsam, Steve, Kolvenbach, Caroline M., Merz, Lea Maria, Mertens, Nils D., Hermle, Tobias, Mann, Nina, Pantel, Dalia, Halawi, Abdul A., Bao, Aaron, Schierbaum, Luca, Schneider, Sophia, Salmanullah, Daanya, Ben-Dov, Iddo Z., Sagiv, Itamar, Eid, Loai A., Awad, Hazem Subhi H., Al Saffar, Muna, Soliman, Neveen A., Nabhan, Marwa M., Kari, Jameela A., El Desoky, Sherif, Shalaby, Mohamed A., Ooda, Said, Fathy, Hanan M., Mane, Shrikant, Lifton, Richard P., Somers, Michael J.G., Hildebrandt, Friedhelm

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Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice von Majmundar, Amar J., Buerger, Florian, Forbes, Thomas A., Klambt, Verena, Schneider, Ronen, Deutsch, Konstantin, Kitzler, Thomas M., Howden, Sara E., Scurr, Michelle, Tan, Ker Sin, Krzeminski, Mickael, Widmeier, Eugen, Braun, Daniela A., Lai, Ethan, Ullah, Ihsan, Amar, Ali, Kolb, Amy, Eddy, Kaitlyn, Chen, Chin Heng, Salmanullah, Daanya, Dai, Rufeng, Nakayama, Makiko, Ottlewski, Isabel, Kolvenbach, Caroline M., Onuchic-Whitford, Ana C., Mao, Youying, Mann, Nina, Nabhan, Marwa M., Rosen, Seymour, Forman-Kay, Julie D., Soliman, Neveen A., Heilos, Andreas, Kain, Renate, Aufricht, Christoph, Mane, Shrikant, Lifton, Richard P., Shril, Shirlee, Little, Melissa H., Hildebrandt, Friedhelm

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Clinical utility of chitotriosidase enzyme activity in nephropathic cystinosis von Elmonem, Mohamed A, Makar, Samuel H, van den Heuvel, Lambertus, Abdelaziz, Hanan, Abdelrahman, Safaa M, Bossuyt, Xavier, Janssen, Mirian C, Cornelissen, Elisabeth Am, Lefeber, Dirk J, Joosten, Leo Ab, Nabhan, Marwa M, Arcolino, Fanny O, Hassan, Fayza A, Gaide Chevronnay, Héloïse P, Soliman, Neveen A, Levtchenko, Elena

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Soluble adhesion molecules as markers of native arteriovenous fistula thrombosis in children on uremia von Fadel, Fatina I, Elshamaa, Manal F, Nabhan, Marwa M, Essam, Rascha G, Kantoush, Nagwa, El Sonbaty, Marwa M, Raafat, Mona, Abd-El Haleem, Dalia A

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Clinical and ultrasonographical characterization of childhood cystic kidney diseases in Egypt von Soliman, Neveen A., Nabhan, Marwa M., Bazaraa, Hafez M., Badr, Ahmed M., Shaheen, Mohamed

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Homozygous NPHP1 deletions in Egyptian children with nephronophthisis including an infantile onset patient von Soliman, Neveen A., Hildebrandt, Friedhelm, Allen, Susan J., Otto, Edgar A., Nabhan, Marwa M., Badr, Ahmed M.

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SP905CLINICAL PHENOTYPES OF POLYCYSTIC KIDNEY DISEASE IN EGYPTIAN CHILDREN von Nabhan, Marwa M, Soliman, Neveen A, Bazaraa, Hafez M

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SP889RENAL AND RETINAL PHENOTYPING IN A COHORT OF BARDET-BIEDL SYNDROME von Nabhan, Marwa M, Elfayoumi, Dina, Helmy, Rasha, Soliman, Neveen A

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Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease von Burgmaier, Kathrin, Kunzmann, Kevin, Bergmann, Carsten, Buescher, Anja Katrin, Burgmaier, Mathias, Dursun, Ismail, Eid, Loai, Feldkoetter, Markus, Galiano, Matthias, Geßner, Michaela, Goebel, Heike, Hooman, Nakysa, Jankauskiene, Augustina, Klaus, Guenter, König, Jens, Massella, Laura, Mekahli, Djalila, Melek, Engin, Mir, Sevgi, Pape, Lars, Prikhodina, Larisa, Ranchin, Bruno, Schild, Raphael, Seeman, Tomas, Sever, Lale, Shroff, Rukshana, Soliman, Neveen A., Stabouli, Stella, Taranta-Janusz, Katarzyna, Testa, Sara, Thumfart, Julia, Topaloglu, Rezan, Weber, Lutz Thorsten, Wicher, Dorota, Wygoda, Simone, Yilmaz, Alev, Zachwieja, Katarzyna, Zagozdzon, Ilona, Ranguelov, Nadejda, Collard, Laure, Lombet, Jacques, Maquet, Julie, Schalk, Gesa, Beck, Bodo B., Benzing, Thomas, Buettner, Reinhard, Grundmann, Franziska, Kurschat, Christine, Benz, Kerstin, Tzschoppe, Anja, Buchholz, Björn, Buescher, Rainer, Häffner, Karsten, Krügel, Jenny, Stock, Johanna, Oh, Jun, Vinke, Tobias, Sander, Anja, Henn, Michael, Derichs, Ute, Jeck, Nikola, Lange-Sperandio, Bärbel, Kusser, Franziska, Benz, Marcus, Schmidt, Silke, Huppertz-Kessler, Christina, Titieni, Andrea, Wurm, Donald, Billing, Heiko, Nabhan, Marwa M., Lara, Luis Enrique, Papachristou, Fotios, Emma, Francesco, Cerkauskiene, Rimante, Azukaitis, Karolis, Wasilewska, Anna, Balasz-Chmielewska, Irena, Miklaszewska, Monika, Tkaczyk, Marcin, Sikora, Przemyslaw, Zaniew, Marcin, Antoniewicz, Jolanta, Lesiak, Justyna, Afonso, Alberto Caldas, Teixeira, Ana, Paripović, Dusan, Peco-Antic, Amira, Papizh, Svetlana, Bayazit, Aysun Karabay, Anarat, Ali, Kavukcu, Salih, Candan, Cengiz, Caliskan, Salim, Canpolat, Nur, Emre, Sevinc, Akinci, Nurver, Conkar, Secil, Poyrazoglu, Hakan M., Dötsch, Jörg, Schaefer, Franz

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Nutritional Assessment before and after Nutritional counseling of Children with End Stage Kidney Disease on Regular Hemodialysis von Ghobrial, Emad E, Aboulghar, Hanna M, Khalil Abdel Khalek Mohamed, Nabhan, Marwa M, Ibrahim, Marwa A, Nermin Mohamed Abd El Rahman

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Clinical utility of chitotriosidase enzyme in nephropathic cystinosis von Ibrahim, Mohamed, Makar, Samuel H, van den Heuvel, Bert, Abdelaziz, Hanan, Abdelrahman, Safaa M, Bossuyt, Xavier, Janssen, Mirian C, Cornelissen, Elisabeth A.M, Lefeber, Dirk J, Joosten, Leo A.B, Nabhan, Marwa M, Arcolino, Fanny O, Hassan, Fayza A, Gaide Chevronnay, Heloise P, Soliman, Neveen A, Levtchenko, Elena

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Corticosteroids for improving patient-relevant outcomes in HELLP syndrome: a systematic review and meta-analysis von Kasem, Asmaa F, Alqenawy, Hamdy B, Elgendi, Marwa A, Ali, Radwa R, Ahmed, Rania Hm, Sorour, Mohammad N, Hegab, Khadiga Mh, El-Skaan, Rania G, El Helw, Rowyna H, Elsewefy, Mohamed S, Abdelrazek, Maya M, Elrefaey, Yasser M, Albahaie, Mohamed Yg, Salama, Mohamed H, Nabhan, Ashraf F

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Left ventricular mass index and subendocardial myocardial function in children with chronic kidney disease, a transmural strain and three-dimensional echocardiographic study von El Tantawy, Amira Esmat, Fadel, Fatina, Abdelrahman, Safaa M, Nabhan, Marwa, Ibrahim, Reem, Fattouh, Aya M, Sayed, Shaimaa, ElKhashab, Khaled Mohamed, Afdal, Peter, AbdelMassih, Antoine Fakhry

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