Search Results - Vanderver, Adeline

Phenotypic and imaging spectrum associated wth WDR45 by Adang, Laura A. (Author) , Pizzino, Amy (Author) , Malhotra, Alka (Author) , Dubbs, Holly (Author) , Williams, Catherine (Author) , Sherbini, Omar (Author) , Anttonen, Anna-Kaisa (Author) , Lesca, Gaetan (Author) , Linnankivi, Tarja (Author) , Laurencin, Chloé (Author) , Milh, Matthieu (Author) , Perrine, Charles (Author) , Schaaf, Christian P. (Author) , Poulat, Anne-Lise (Author) , Ville, Dorothee (Author) , Hagelstrom, Tanner (Author) , Perry, Denise L. (Author) , Taft, Ryan J. (Author) , Goldstein, Amy (Author) , Vossough, Arastoo (Author) , Helbig, Ingo (Author) , Vanderver, Adeline (Author) ,

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

Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expression by Giorgio, Elisa (Author) , Rolyan, Harshvardhan (Author) , Kropp, Laura (Author) , Chakka, Anish Baswanth (Author) , Yatsenko, Svetlana (Author) , Gregorio, Eleonora Di (Author) , Lacerenza, Daniela (Author) , Vaula, Giovanna (Author) , Talarico, Flavia (Author) , Mandich, Paola (Author) , Toro, Camilo (Author) , Pierre, Eleonore Eymard (Author) , Labauge, Pierre (Author) , Capellari, Sabina (Author) , Cortelli, Pietro (Author) , Vairo, Filippo Pinto (Author) , Miguel, Diego (Author) , Stubbolo, Danielle (Author) , Marques, Lourenco Charles (Author) , Gahl, William (Author) , Boespflug‐Tanguy, Odile (Author) , Melberg, Atle (Author) , Hassin‐Baer, Sharon (Author) , Cohen, Oren S. (Author) , Pjontek, Rastislav (Author) , Grau, Armin J. (Author) , Klopstock, Thomas* (Author) , Fogel, Brent (Author) , Meijer, Inge (Author) , Rouleau, Guy (Author) , Bouchard, Jean-Pierre L. (Author) , Ganapathiraju, Madhavi (Author) , Vanderver, Adeline (Author) , Dahl, Niklas (Author) , Hobson, Grace (Author) , Brusco, Alfredo (Author) , Brussino, Alessandro (Author) , Padiath, Quasar Saleem (Author) ,

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

NUBPL mutations in patients with complex I deficiency and a distinct MRI pattern by Kevelam, Sietske H. (Author) , Rodenburg, Richard J. (Author) , Wolf, Nicole I. (Author) , Ferreira, Patrick (Author) , Lunsing, Roelineke J. (Author) , Nijtmans, Leo G. (Author) , Mitchell, Anne (Author) , Arroyo, Hugo A. (Author) , Rating, Dietz (Author) , Vanderver, Adeline (Author) , Berkel, Carola G. M. van (Author) , Abbink, Truus E. M. (Author) , Heutink, Peter (Author) , Knaap, Marjo S. van der (Author) ,

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