Impressions from riemann’s native country von Laugwitz, Annette, Laugwitz, Detlef

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Probing the Y2 Receptor on Transmembrane, Intra- and Extra-Cellular Sites for EPR Measurements von Laugwitz, Jeannette M., Haeri, Haleh H., Kaiser, Anette, Krug, Ulrike, Hinderberger, Dariush, Beck-Sickinger, Annette G., Schmidt, Peter

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Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes von Laugwitz, Lucia, Seibt, Annette, Herebian, Diran, Peralta, Susana, Steinfeld, Robert, Joset, Pascal, Steindl, Katharina, Rauch, Anita

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Cis-epistasis at the LPA locus and risk of cardiovascular diseases von Zeng, Lingyao, Moser, Sylvain, Mirza-Schreiber, Nazanin, Lamina, Claudia, Coassin, Stefan, Nelson, Christopher P, Annilo, Tarmo, Franzén, Oscar, Kleber, Marcus E, Mack, Salome, Andlauer, Till F M, Jiang, Beibei, Stiller, Barbara, Li, Ling, Willenborg, Christina, Munz, Matthias, Kessler, Thorsten, Kastrati, Adnan, Laugwitz, Karl-Ludwig, Erdmann, Jeanette, Moebus, Susanne, Nöthen, Markus M, Peters, Annette, Strauch, Konstantin, Müller-Nurasyid, Martina, Gieger, Christian, Meitinger, Thomas, Steinhagen-Thiessen, Elisabeth, März, Winfried, Metspalu, Andres, Björkegren, Johan L M, Samani, Nilesh J, Kronenberg, Florian, Müller-Myhsok, Bertram, Schunkert, Heribert

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It Is Not Carved in Stone-The Need for a Genetic Reevaluation of Variants in Pediatric Cardiomyopathies von Westphal, Dominik Sebastian, Pollmann, Kathrin, Marschall, Christoph, Wacker-Gussmann, Annette, Oberhoffer-Fritz, Renate, Laugwitz, Karl-Ludwig, Ewert, Peter, Wolf, Cordula Maria

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Bi‐Allelic COQ4 Variants Cause Adult‐Onset Ataxia‐Spasticity Spectrum Disease von Cordts, Isabell, Semmler, Luisa, Prasuhn, Jannik, Seibt, Annette, Herebian, Diran, Navaratnarajah, Tharsini, Park, Joohyun, Deininger, Natalie, Laugwitz, Lucia, Göricke, Sophia L., Lingor, Paul, Brüggemann, Norbert, Münchau, Alexander, Synofzik, Matthis, Timmann, Dagmar, Mayr, Johannes A., Haack, Tobias B., Distelmaier, Felix, Deschauer, Marcus

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ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations von Laugwitz, Lucia, Cheng, Fubo, Collins, Stephan C, Hustinx, Alexander, Navarro, Nicolas, Welsch, Simon, Cox, Helen, Hsieh, Tzung-Chien, Vijayananth, Aswinkumar, Buchert, Rebecca, Bender, Benjamin, Efthymiou, Stephanie, Murphy, David, Zafar, Faisal, Rana, Nuzhat, Grasshoff, Ute, Falb, Ruth J, Grimmel, Mona, Seibt, Annette, Zheng, Wenxu, Ghaedi, Hamid, Thirion, Marie, Couette, Sébastien, Azizimalamiri, Reza, Sadeghian, Saeid, Galehdari, Hamid, Zamani, Mina, Zeighami, Jawaher, Sedaghat, Alireza, Ramshe, Samira Molaei, Zare, Ali, Alipoor, Behnam, Klee, Dirk, Sturm, Marc, Ossowski, Stephan, Houlden, Henry, Riess, Olaf, Wieczorek, Dagmar, Gavin, Ryan, Maroofian, Reza, Krawitz, Peter, Yalcin, Binnaz, Distelmaier, Felix, Haack, Tobias B

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Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management von Laugwitz, Lucia, Schoenmakers, Daphne H., Adang, Laura A., Beck-Woedl, Stefanie, Bergner, Caroline, Bernard, Geneviève, Bley, Annette, Boyer, Audrey, Calbi, Valeria, Dekker, Hanka, Eichler, Florian, Eklund, Erik, Fumagalli, Francesca, Gavazzi, Francesco, Grønborg, Sabine W., van Hasselt, Peter, Langeveld, Mirjam, Lindemans, Caroline, Mochel, Fanny, Oberg, Andreas, Ram, Dipak, Saunier-Vivar, Elise, Schöls, Ludger, Scholz, Michael, Sevin, Caroline, Zerem, Ayelet, Wolf, Nicole I., Groeschel, Samuel

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Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management von Laugwitz, Lucia, Schoenmakers, Daphne H, Adang, Laura A, Beck-Woedl, Stefanie, Bergner, Caroline, Bernard, Geneviève, Bley, Annette, Boyer, Audrey, Calbi, Valeria, Dekker, Hanka, Eichler, Florian, Eklund, Erik, Fumagalli, Francesca, Gavazzi, Francesco, Grønborg, Sabine W, van Hasselt, Peter, Langeveld, Mirjam, Lindemans, Caroline, Mochel, Fanny, Oberg, Andreas, Ram, Dipak, Saunier-Vivar, Elise, Schöls, Ludger, Scholz, Michael, Sevin, Caroline, Zerem, Ayelet, Wolf, Nicole I, Groeschel, Samuel

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Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States von Adang, Laura A., Bonkowsky, Joshua L., Boelens, Jaap Jan, Mallack, Eric, Ahrens-Nicklas, Rebecca, Bernat, John A., Bley, Annette, Burton, Barbara, Darling, Alejandra, Eichler, Florian, Eklund, Erik, Emrick, Lisa, Escolar, Maria, Fatemi, Ali, Fraser, Jamie L., Gaviglio, Amy, Keller, Stephanie, Patterson, Marc C., Orchard, Paul, Orthmann-Murphy, Jennifer, Santoro, Jonathan D., Schöls, Ludger, Sevin, Caroline, Srivastava, Isha N., Rajan, Deepa, Rubin, Jennifer P., Van Haren, Keith, Wasserstein, Melissa, Zerem, Ayelet, Fumagalli, Francesca, Laugwitz, Lucia, Vanderver, Adeline

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Probing the Y(2)Receptor on Transmembrane, Intra- and Extra-Cellular Sites for EPR Measurements von Laugwitz, Jeannette M., Haeri, Haleh H., Kaiser, Anette, Krug, Ulrike, Hinderberger, Dariush, Beck-Sickinger, Annette G., Schmidt, Peter

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Probing the Y 2 Receptor on Transmembrane, Intra- and Extra-Cellular Sites for EPR Measurements von Laugwitz, Jeannette M, Haeri, Haleh H, Kaiser, Anette, Krug, Ulrike, Hinderberger, Dariush, Beck-Sickinger, Annette G, Schmidt, Peter

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ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations von Laugwitz, Lucia, Cheng, Fubo, Collins, Stephan C, Hustinx, Alexander, Navarro, Nicolas, Welsch, Simon, Cox, Helen, Hsieh, Tzung-Chien, Vijayananth, Aswinkumar, Buchert, Rebecca, Bender, Benjamin, Efthymiou, Stephanie, Murphy, David, Zafar, Faisal, Rana, Nuzhat, Grasshoff, Ute, Falb, Ruth J, Grimmel, Mona, Seibt, Annette, Zheng, Wenxu, Ghaedi, Hamid, Thirion, Marie, Couette, Sébastien, Azizimalamiri, Reza, Sadeghian, Saeid, Galehdari, Hamid, Zamani, Mina, Zeighami, Jawaher, Sedaghat, Alireza, Ramshe, Samira Molaei, Zare, Ali, Alipoor, Behnam, Klee, Dirk, Sturm, Marc, Ossowski, Stephan, Houlden, Henry, Riess, Olaf, Wieczorek, Dagmar, Gavin, Ryan, Maroofian, Reza, Krawitz, Peter, Yalcin, Binnaz, Distelmaier, Felix, Haack, Tobias B

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