Search Results - Wurm, Donald

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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Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies by Morava-Kozicz, Eva (Author) , Tiemes, Vera (Author) , Thiel, Christian (Author) , Seta, Nathalie (Author) , Lonlay, Pascale de (Author) , Klerk, Hans de (Author) , Mulder, Margot (Author) , Rubio‐Gozalbo, Estela (Author) , Visser, Gepke (Author) , Hasselt, Peter van (Author) , Horovitz, Dafne D. G. (Author) , Souza, Carolina Fischinger Moura de (Author) , Schwartz, Ida V. D. (Author) , Green, Andrew (Author) , Al‐Owain, Mohammed (Author) , Uziel, Graciella (Author) , Sigaudy, Sabine (Author) , Chabrol, Brigitte (Author) , Spronsen, Franc-Jan van (Author) , Steinert, Martin (Author) , Komini, Eleni (Author) , Wurm, Donald (Author) , Bevot, Andrea (Author) , Ayadi, Addelkarim (Author) , Huijben, Karin (Author) , Dercksen, Marli (Author) , Witters, Peter (Author) , Jaeken, Jaak (Author) , Matthijs, Gert (Author) , Lefeber, Dirk J. (Author) , Wevers, Ron A. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies by Morava-Kozicz, Eva (Author) , Tiemes, Vera (Author) , Thiel, Christian (Author) , Seta, Nathalie (Author) , Lonlay, Pascale de (Author) , Klerk, Hans de (Author) , Mulder, Margot (Author) , Rubio‐Gozalbo, Estela (Author) , Visser, Gepke (Author) , Hasselt, Peter van (Author) , Horovitz, Dafne D. G. (Author) , Souza, Carolina Fischinger Moura de (Author) , Schwartz, Ida V. D. (Author) , Green, Andrew (Author) , Al‐Owain, Mohammed (Author) , Uziel, Graciella (Author) , Sigaudy, Sabine (Author) , Chabrol, Brigitte (Author) , Spronsen, Franc-Jan van (Author) , Steinert, Martin (Author) , Komini, Eleni (Author) , Wurm, Donald (Author) , Bevot, Andrea (Author) , Ayadi, Addelkarim (Author) , Huijben, Karin (Author) , Dercksen, Marli (Author) , Witters, Peter (Author) , Jaeken, Jaak (Author) , Matthijs, Gert (Author) , Lefeber, Dirk J. (Author) , Wevers, Ron A. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext