Search Results - Morin, Denis

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  1. 1

    Renal and extrarenal phenotypes in patients with HNF1B variants and chromosome 17q12 microdeletions by Buffin-Meyer, Bénédicte (Author) , Richard, Juliette (Author) , Guigonis, Vincent (Author) , Weber, Stefanie (Author) , König, Jens (Author) , Heidet, Laurence (Author) , Moussaoui, Nabila (Author) , Vu, Jeanne-Pierrette (Author) , Faguer, Stanislas (Author) , Casemayou, Audrey (Author) , Prakash, Richa (Author) , Baudouin, Véronique (Author) , Hogan, Julien (Author) , Alexandrou, Demi (Author) , Bockenhauer, Detlef (Author) , Bacchetta, Justine (Author) , Ranchin, Bruno (Author) , Pruhova, Stepanka (Author) , Zieg, Jakub (Author) , Lahoche, Annie (Author) , Okorn, Christine (Author) , Antal-Kónya, Violetta (Author) , Morin, Denis (Author) , Becherucci, Francesca (Author) , Habbig, Sandra (Author) , Liebau, Max C. (Author) , Mauras, Mathilde (Author) , Nijenhuis, Tom (Author) , Llanas, Brigitte (Author) , Mekahli, Djalila (Author) , Thumfart, Julia (Author) , Tönshoff, Burkhard (Author) , Massella, Laura (Author) , Eckart, Philippe (Author) , Cloarec, Sylvie (Author) , Cruz, Alejandro (Author) , Patzer, Ludwig (Author) , Roussey, Gwenaelle (Author) , Vrillon, Isabelle (Author) , Dunand, Olivier (Author) , Bessenay, Lucie (Author) , Taroni, Francesca (Author) , Zaniew, Marcin (Author) , Louillet, Ferielle (Author) , Bergmann, Carsten (Author) , Schaefer, Franz (Author) , van Eerde, Albertien M. (Author) , Schanstra, Joost P. (Author) , Decramer, Stéphane (Author) , Ariceta, Gema (Author) , Benetti, Elisa (Author) , Benz, Marcus R. (Author) , Bjerre, Anna (Author) , Boudailliez, Bernard R. (Author) , Bouts, Antonia (Author) , Drube, Jens (Author) , Gjerstad, Ann Christin (Author) , Jankauskiene, Augustina (Author) , Jávorszky, Eszter (Author) , Jay, Nadine (Author) , Kirschstein, Martin (Author) , Varda, Nataša Marčun (Author) , Niel, Olivier (Author) , Nobili, François (Author) , Pietrement, Christine (Author) , Ruzgiene, Dovile (Author) , Schild, Raphael (Author) , Staude, Hagen (Author) , Tory, Kálmán (Author) , Tsimaratos, Michel (Author) , Walden, Ulrike (Author) , Zappel, Hildegard (Author) ,


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  2. 2

    Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants by Burgmaier, Kathrin (Author) , Brinker, Leonie (Author) , Erger, Florian (Author) , Beck, Bodo B. (Author) , Benz, Marcus R. (Author) , Bergmann, Carsten (Author) , Boyer, Olivia (Author) , Collard, Laure (Author) , Dafinger, Claudia (Author) , Fila, Marc (Author) , Kowalewska, Claudia (Author) , Lange-Sperandio, Bärbel (Author) , Massella, Laura (Author) , Mastrangelo, Antonio (Author) , Mekahli, Djalila (Author) , Miklaszewska, Monika (Author) , Ortiz-Bruechle, Nadina (Author) , Patzer, Ludwig (Author) , Prikhodina, Larisa (Author) , Ranchin, Bruno (Author) , Ranguelov, Nadejda (Author) , Schild, Raphael (Author) , Seeman, Tomas (Author) , Sever, Lale (Author) , Sikora, Przemyslaw (Author) , Szczepanska, Maria (Author) , Teixeira, Ana (Author) , Thumfart, Julia (Author) , Uetz, Barbara (Author) , Weber, Lutz Thorsten (Author) , Wühl, Elke (Author) , Zerres, Klaus (Author) , Dötsch, Jörg (Author) , Schaefer, Franz (Author) , Liebau, Max Christoph (Author) , Eid, Loai Akram (Author) , Arbeiter, Klaus (Author) , Godefroid, Nathalie (Author) , Lombet, Jacques (Author) , De Mul, Aurélie (Author) , Feldkoetter, Markus (Author) , Zieg, Jakub (Author) , Grundmann, Franziska (Author) , Galiano, Matthias (Author) , Buchholz, Björn (Author) , Buescher, Anja (Author) , Häffner, Karsten (Author) , Gross, Oliver (Author) , Oh, Jun (Author) , Haffner, Dieter (Author) , Bernhardt, Wanja (Author) , Schäfer, Susanne (Author) , Wygoda, Simone (Author) , Halbritter, Jan (Author) , Derichs, Ute (Author) , Klaus, Günter (Author) , Lechner, Felix (Author) , Ponsel, Sabine (Author) , König, Jens (Author) , Staude, Hagen (Author) , Wurm, Donald (Author) , Bald, Martin (Author) , Gessner, Michaela (Author) , Soliman, Neveen A. (Author) , Ariceta, Gema (Author) , Gonzalez Rodriguez, Juan David (Author) , Ojeda, Francisco de la Cerda (Author) , Harambat, Jerome (Author) , Morin, Denis (Author) , Dossier, Claire (Author) , Dorval, Guillaume (Author) , Shroff, Rukshana (Author) , Stabouli, Stella (Author) , Hooman, Nakysa (Author) , Mencarelli, Francesca (Author) , Morello, William (Author) , Longo, Germana (Author) , Emma, Francesco (Author) , Jankauskiene, Augustina (Author) , Taranta-Janusz, Katarzyna (Author) , Zagozdzon, Ilona (Author) , Zachwieja, Katarzyna (Author) , Stanczyk, Malgorzata (Author) , Bienias, Beata (Author) , Litwin, Mieczyslaw (Author) , Morawiec-Knysak, Aurelia (Author) , Afonso, Alberto Caldas (Author) , Dunand, Oliver (Author) , Rachisan, Andreea (Author) , Miloševski-Lomić, Gordana (Author) , Papizh, Svetlana (Author) , Rus, Rina (Author) , Jilani, Houweyda (Author) , Atmis, Bahriye (Author) , Duzova, Ali (Author) , Soylu, Alper (Author) , Candan, Cengiz (Author) , Caliskan, Salim (Author) , Yilmaz, Alev (Author) , Gökce, İbrahim (Author) , Akinci, Nurver (Author) , Mir, Sevgi (Author) , Dursun, Ismail (Author) , Tabel, Yilmaz (Author) , Nalcacioglu, Hulya (Author) ,


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  3. 3

    Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome by Lemaire, Mathieu (Author) , Frémeaux-Bacchi, Véronique (Author) , Schaefer, Franz (Author) , Choi, Murim (Author) , Tang, Wai Ho (Author) , Le Quintrec, Moglie (Author) , Fakhouri, Fadi (Author) , Taque, Sophie (Author) , Nobili, François (Author) , Martinez, Frank (Author) , Ji, Weizhen (Author) , Overton, John D. (Author) , Mane, Shrikant M. (Author) , Nürnberg, Gudrun (Author) , Altmüller, Janine (Author) , Thiele, Holger (Author) , Morin, Denis (Author) , Deschenes, Georges (Author) , Baudouin, Véronique (Author) , Llanas, Brigitte (Author) , Collard, Laure (Author) , Majid, Mohammed A. (Author) , Simkova, Eva (Author) , Nürnberg, Peter (Author) , Rioux-Leclerc, Nathalie (Author) , Moeckel, Gilbert W. (Author) , Gubler, Marie Claire (Author) , Hwa, John (Author) , Loirat, Chantal (Author) , Lifton, Richard P. (Author) ,


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