Хайлтын үр дүнгүүд - Guillaume Dorval

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  1. 1
    Response to First Course of Intensified Immunosuppression in Genetically Stratified Steroid Resistant Nephrotic Syndrome

    Response to First Course of Intensified Immunosuppression in Genetically Stratified Steroid Resistant Nephrotic Syndrome -н Anna E. Mason, Ethan S. Sen, Agnieszka Bierżyńska, Elizabeth Colby, Maryam Afzal, Guillaume Dorval, Ania Koziell, Maggie Williams, Olivia Boyer, Gavin I. Welsh, Moin A. Saleem

    Хэвлэсэн 2020
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    Artigo
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  2. 2
    TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways

    TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways -н Guillaume Dorval, Valeryia Kuzmuk, Olivier Gribouval, Gavin I. Welsh, Agnieszka Bierżyńska, Alain Schmitt, Stéphanie Miserey‐Lenkei, Ania Koziell, Shuman Haq, Alexandre Benmerah, Géraldine Mollet, Olivia Boyer, Moin A. Saleem, Corinne Antignac

    Хэвлэсэн 2019
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    Artigo
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  3. 3
    Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children

    Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children -н Mathilde Glénisson, Mathilde Grapin, Thomas Blanc, Evgenia Preka, Julien Hogan, Manon Aurelle, G. Roussey, Antoine Mouche, Caroline Rousset‐Rouvière, Robert Novo, Camille Faudeux, Marc Fila, Isabelle Vrillon, Sylvie Cloarec, Tabassome Simon, Jérôme Harambat, Edouard Martinez Casado, Julien Rod, Morgane Carre Lecoindre, Laurence Heidet, Olivia Boyer, Nicolas Garcelon, Jessica Kachmar, Guillaume Dorval, Sabine Sarnacki

    Хэвлэсэн 2025
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    Artigo
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  4. 4
    Long-Term Efficacy and Safety of Repeated Rituximab to Maintain Remission in Idiopathic Childhood Nephrotic Syndrome: An International Study

    Long-Term Efficacy and Safety of Repeated Rituximab to Maintain Remission in Idiopathic Childhood Nephrotic Syndrome: An International Study -н Eugene Yu-hin Chan, E. Yu, Andrea Angeletti, Zainab Arslan, Biswanath Basu, Olivia Boyer, Chang‐Yien Chan, Manuela Colucci, Guillaume Dorval, Claire Dossier, Stefania Drovandi, Gian Marco Ghiggeri, Debbie S. Gipson, Riku Hamada, Julien Hogan, Kenji Ishikura, Koichi Kamei, Markus J. Kemper, Alison Lap‐tak, Rulan S. Parekh, Seetha Radhakrishnan, Priya Saini, Qian Shen, Rajiv Sinha, Chantida Subun, Sharon Teo, Marina Vivarelli, Hazel Webb, Hong Xu, Hui‐Kim Yap, Kjell Tullus

    Хэвлэсэн 2022
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    Artigo
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  5. 5
    Pseudouridylation defect due to <i>DKC1</i> and <i>NOP10</i> mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis

    Pseudouridylation defect due to <i>DKC1</i> and <i>NOP10</i> mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis -н Eszter Balogh, Jennifer C. Chandler, Máté Varga, Mona Tahoun, Dóra K. Menyhárd, Gusztáv Schay, Tomas Goncalves, Renáta Hamar, Regina Légrádi, Ákos Szekeres, Olivier Gribouval, Robert Kleta, Horia Stanescu, Detlef Böckenhauer, Andrea Kerti, Hywel Williams, Veronica A. Kinsler, Wei‐Li Di, David Curtis, Maria Kolatsi‐Joannou, Hafsa Hammid, Anna Szőcs, Kristóf Perczel, Erika Maka, Gergely Toldi, Florentina Sava, Christelle Arrondel, Magdolna Kardos, Attila Fintha, Ahmed Hossain, Felipe D’Arco, Marios Kaliakatsos, Jutta Köeglmeier, William Mifsud, Mariya Moosajee, Ana Faro, Eszter Jávorszky, Gábor Rudas, Marwa H. Saied, Salah Marzouk, Kata Kelen, Judit Götze, György Reusz, Tivadar Tulassay, François Dragon, Géraldine Mollet, Susanne Motameny, Hölger Thiele, Guillaume Dorval, Peter Nürnberg, András Perczel, Attila J. Szabó, David A. Long, Kazunori Tomita, Corinne Antignac, Aoife Waters, Kálmán Tory

    Хэвлэсэн 2020
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    Artigo
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  6. 6
    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 -н 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

    Хэвлэсэн 2021
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    Artigo
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