Accumulation of APP C-terminal fragments causes endolysosomal dysfunction through the dysregulation of late endosome to lysosome-ER contact sites von Bretou, Marine, Sannerud, Ragna, Escamilla-Ayala, Abril, Leroy, Tom, Vrancx, Celine, Van Acker, Zoe P, Perdok, Anika, Vermeire, Wendy, Vorsters, Inge, Van Keymolen, Sophie, Maxson, Michelle, Pavie, Benjamin, Wierda, Keimpe, Eskelinen, Eeva-Liisa, Annaert, Wim

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Accumulation of APP C-terminal fragments causes endolysosomal dysfunction through the dysregulation of late endosome to lysosome-ER contact sites von Bretou, Marine, Sannerud, Ragna, Escamilla-Ayala, Abril, Leroy, Tom, Vrancx, Céline, Van Acker, Zoë P., Perdok, Anika, Vermeire, Wendy, Vorsters, Inge, Van Keymolen, Sophie, Maxson, Michelle, Pavie, Benjamin, Wierda, Keimpe, Eskelinen, Eeva-Liisa, Annaert, Wim

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SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies von Bissay, Véronique, Van Malderen, Sophie C H, Keymolen, Kathelijn, Lissens, Willy, Peeters, Uschi, Daneels, Dorien, Jansen, Anna C, Pappaert, Gudrun, Brugada, Pedro, De Keyser, Jacques, Van Dooren, Sonia

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