Study of selected mild steels for application in vacuum systems of future gravitational wave detectors von Scarcia, Carlo, Bregliozzi, Giuseppe, Chiggiato, Paolo, Ingrid Michet, Alice, Perez Fontenla, Ana Teresa, Rimoldi, Martino, Taborelli, Mauro, Wevers, Ivo

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Study of selected mild steels for application in vacuum systems of future gravitational wave detectors von Scarcia, Carlo, Bregliozzi, Giuseppe, Chiggiato, Paolo, Michet, Alice Ingrid, Perez Fontenla, Ana Teresa, Rimoldi, Martino, Taborelli, Mauro, Wevers, Ivo

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Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system von Feyen, Jacqueline, Ping, Zhen, Chen, Lanpeng, van Dijk, Claire, van Tienhoven, Tim V. D., van Strien, Paulina M. H., Hoogenboezem, Remco M., Wevers, Michiel J. W., Sanders, Mathijs A., Touw, Ivo P., Raaijmakers, Marc H. G. P.

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Is Hypoxia Related to External Cervical Resorption? A Case Report von Mavridou, Athina Maria, Hilkens, Petra, Lambrichts, Ivo, Hauben, Esther, Wevers, Martine, Bergmans, Lars, Lambrechts, Paul

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Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness von Wortmann, Saskia B, Vaz, Frédéric M, Gardeitchik, Thatjana, Vissers, Lisenka E L M, Renkema, G Herma, Schuurs-Hoeijmakers, Janneke H M, Kulik, Wim, Lammens, Martin, Christin, Christin, Kluijtmans, Leo A J, Rodenburg, Richard J, Nijtmans, Leo G J, Grünewald, Anne, Klein, Christine, Gerhold, Joachim M, Kozicz, Tamas, van Hasselt, Peter M, Harakalova, Magdalena, Kloosterman, Wigard, Barić, Ivo, Pronicka, Ewa, Ucar, Sema Kalkan, Naess, Karin, Singhal, Kapil K, Krumina, Zita, Gilissen, Christian, van Bokhoven, Hans, Veltman, Joris A, Smeitink, Jan A M, Lefeber, Dirk J, Spelbrink, Johannes N, Wevers, Ron A, Morava, Eva, de Brouwer, Arjan P M

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Abnormal concentrations of acetylated amino acids in cerebrospinal fluid in acetyl‐CoA transporter deficiency von Šikić, Katarina, Peters, Tessa M. A., Marušić, Eugenija, Čagalj, Ivana Čulo, Ramadža, Danijela Petković, Žigman, Tamara, Fumić, Ksenija, Fernandez, Esperanza, Gevaert, Kris, Debeljak, Željko, Wevers, Ron A., Barić, Ivo

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Succinic semialdehyde dehydrogenase deficiency in mice and in humans: An untargeted metabolomics perspective von Peters, Tessa M. A., Engelke, Udo F. H., Boer, Siebolt, Reintjes, Joris T. G., Roullet, Jean‐Baptiste, Broekman, Sanne, Vrieze, Erik, Wijk, Erwin, Wamelink, Mirjam M. C., Artuch, Rafael, Barić, Ivo, Merx, Jona, Boltje, Thomas J., Martens, Jonathan, Willemsen, Michèl A. A. P., Verbeek, Marcel M., Wevers, Ron A., Gibson, K. Michael, Coene, Karlien L. M.

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The genotypic and phenotypic spectrum of MTO1 deficiency von O'Byrne, James J., Tarailo-Graovac, Maja, Ghani, Aisha, Champion, Michael, Deshpande, Charu, Dursun, Ali, Ozgul, Riza K., Freisinger, Peter, Garber, Ian, Haack, Tobias B., Horvath, Rita, Barić, Ivo, Husain, Ralf A., Kluijtmans, Leo A.J., Kotzaeridou, Urania, Morris, Andrew A., Ross, Colin J., Santra, Saikat, Smeitink, Jan, Tarnopolsky, Mark, Wortmann, Saskia B., Mayr, Johannes A., Brunner-Krainz, Michaela, Prokisch, Holger, Wasserman, Wyeth W., Wevers, Ron A., Engelke, Udo F., Rodenburg, Richard J., Ting, Teck Wah, McFarland, Robert, Taylor, Robert W., Salvarinova, Ramona, van Karnebeek, Clara D.M.

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Novel cerebrospinal fluid biomarkers of glucose transporter type 1 deficiency syndrome: Implications beyond the brain's energy deficit von Peters, Tessa M. A., Merx, Jona, Kooijman, Pieter C., Noga, Marek, Boer, Siebolt, Gemert, Loes A., Salden, Guido, Engelke, Udo F. H., Lefeber, Dirk J., Outersterp, Rianne E., Berden, Giel, Boltje, Thomas J., Artuch, Rafael, Pías‐Peleteiro, Leticia, García‐Cazorla, Ángeles, Barić, Ivo, Thöny, Beat, Oomens, Jos, Martens, Jonathan, Wevers, Ron A., Verbeek, Marcel M., Coene, Karlien L. M., Willemsen, Michèl A. A. P.

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Huppke–Brendel syndrome: Novel cases and a therapeutic trial with ketogenic diet and N‐acetylcysteine von Šikić, Katarina, Peters, Tessa M. A., Engelke, Udo, Petković Ramadža, Danijela, Žigman, Tamara, Fumić, Ksenija, Davidović, Maša, Huljev Frković, Sanda, Körmendy, Tibor, Martinelli, Diego, Novelli, Antonio, Lepri, Francesca Romana, Wevers, Ron A., Barić, Ivo

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Progressive deafness–dystonia due to SERAC1 mutations: A study of 67 cases von Maas, Roeltje R., Iwanicka‐Pronicka, Katarzyna, Kalkan Ucar, Sema, Alhaddad, Bader, AlSayed, Moeenaldeen, Al‐Owain, Mohammed A., Al‐Zaidan, Hamad I., Balasubramaniam, Shanti, Barić, Ivo, Bubshait, Dalal K., Burlina, Alberto, Christodoulou, John, Chung, Wendy K., Colombo, Roberto, Darin, Niklas, Freisinger, Peter, Garcia Silva, Maria Teresa, Grunewald, Stephanie, Haack, Tobias B., van Hasselt, Peter M., Hikmat, Omar, Hörster, Friederike, Isohanni, Pirjo, Ramzan, Khushnooda, Kovacs‐Nagy, Reka, Krumina, Zita, Martin‐Hernandez, Elena, Mayr, Johannes A., McClean, Patricia, De Meirleir, Linda, Naess, Karin, Ngu, Lock H., Pajdowska, Magdalena, Rahman, Shamima, Riordan, Gillian, Riley, Lisa, Roeben, Benjamin, Rutsch, Frank, Santer, Rene, Schiff, Manuel, Seders, Martine, Sequeira, Silvia, Sperl, Wolfgang, Staufner, Christian, Synofzik, Matthis, Taylor, Robert W., Trubicka, Joanna, Tsiakas, Konstantinos, Unal, Ozlem, Wassmer, Evangeline, Wedatilake, Yehani, Wolff, Toni, Prokisch, Holger, Morava, Eva, Pronicka, Ewa, Wevers, Ron A., de Brouwer, Arjan P., Wortmann, Saskia B.

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Is Hypoxia Related to External Cervical Resorption? A Case Report von Mavridou, Athina Maria, Hilkens, Petra, Lambrichts, Ivo, Hauben, Esther, Wevers, Martine, Bergmans, Lars, Lambrechts, Paul

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Structural elucidation of novel biomarkers of known metabolic disorders based on multistage fragmentation mass spectra von Václavík, Jan, Coene, Karlien L. M., Vrobel, Ivo, Najdekr, Lukáš, Friedecký, David, Karlíková, Radana, Mádrová, Lucie, Petsalo, Aleksanteri, Engelke, Udo F. H., van Wegberg, Annemiek, Kluijtmans, Leo A. J., Adam, Tomáš, Wevers, Ron A.

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Novel cerebrospinal fluid biomarkers of glucose transporter type 1 deficiency syndrome: Implications beyond the brain's energy deficit von Peters, Tessa M A, Merx, Jona, Kooijman, Pieter C, Noga, Marek, de Boer, Siebolt, van Gemert, Loes A, Salden, Guido, Engelke, Udo F H, Lefeber, Dirk J, van Outersterp, Rianne E, Berden, Giel, Boltje, Thomas J, Artuch, Rafael, Pías-Peleteiro, Leticia, García-Cazorla, Ángeles, Barić, Ivo, Thöny, Beat, Oomens, Jos, Martens, Jonathan, Wevers, Ron A, Verbeek, Marcel M, Coene, Karlien L M, Willemsen, Michèl A A P

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The genotypic and phenotypic spectrum of MTO1 deficiency von O'Byrne, James J, Tarailo-Graovac, Maja, Ghani, Aisha, Champion, Michael, Deshpande, Charu, Dursun, Ali, Ozgul, Riza K, Freisinger, Peter, Garber, Ian, Haack, Tobias B, Horvath, Rita, Barić, Ivo, Husain, Ralf A, Kluijtmans, Leo AJ, Kotzaeridou, Urania, Morris, Andrew A, Ross, Colin J, Santra, Saikat, Smeitink, Jan, Tarnopolsky, Mark, Wortmann, Saskia B, Mayr, Johannes A, Brunner-Krainz, Michaela, Prokisch, Holger, Wasserman, Wyeth W, Wevers, Ron A, Engelke, Udo F, Rodenburg, Richard J, Ting, Teck Wah, McFarland, Robert, Taylor, Robert W, Salvarinova, Ramona, van Karnebeek, Clara DM

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