Search Results - Ianina Scheer
- Showing 1 - 10 results of 10
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Glutamine supplementation in a child with inherited GS deficiency improves the clinical status and partially corrects the peripheral and central amino acid imbalance by Johannes Häberle, Noora Shahbeck, Khalid Ibrahim, Bernhard Schmitt, Ianina Scheer, Ruth Tuura, Farrukh A. Chaudhry, Tawfeg Ben‐Omran
Published 2012Artigo -
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Quantitative Cerebral Perfusion Imaging in Children and Young Adults with Moyamoya Disease: Comparison of Arterial Spin-Labeling-MRI and H2[15O]-PET by Robert Goetti, Geoff Warnock, Félix P. Kuhn, Roman Guggenberger, Ruth Tuura, Andreas K. Buck, Nadia Khan, Ianina Scheer
Published 2013Artigo -
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Cerebral lesions on magnetic resonance imaging correlate with preoperative neurological status in neonates undergoing cardiopulmonary bypass surgery by S. Bertholdt, Beatrice Latal, Rabia Liamlahi, René Prêtre, Ianina Scheer, Robert Goetti, Hitendu Dave, Vera Bernet, A. Schmitz, Michael von Rhein, Walter Knirsch
Published 2013Artigo -
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Delayed cortical gray matter development in neonates with severe congenital heart disease by Nathalie H.P. Claessens, Pim Moeskops, Andreas Buchmann, Beatrice Latal, Walter Knirsch, Ianina Scheer, Ivana Išgum, Linda S. de Vries, Manon J.N.L. Benders, Michael von Rhein
Published 2016Artigo -
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Benchmarking against the MOMS Trial: Zurich Results of Open Fetal Surgery for Spina Bifida by Ueli Möhrlen, Nicole Ochsenbein‐Kölble, Luca Mazzone, Franziska Kraehenmann, M Hüsler, Barbara Casanova, Péter Bíró, David Wille, Beatrice Latal, Ianina Scheer, Vera Bernet, Theres Moehrlen, Leonhard Held, Alan W. Flake, Roland Zimmermann, Martin Meuli
Published 2019Artigo -
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Delineation and Diagnostic Criteria of Oral-Facial-Digital Syndrome Type VI by Andrea Poretti, Giuseppina Vitiello, Raoul C. M. Hennekam, Filippo Arrigoni, Enrico Bertini, Renato Borgatti, Francesco Brancati, Stefano D’Arrigo, Francesca Faravelli, Lucio Giordano, Thierry A.G.M. Huisman, Miriam Iannicelli, Gerhard Kluger, Mårten Kyllerman, Magnus Landgren, Melissa Lees, Lorenzo Pinelli, Romina Romaniello, Ianina Scheer, Christoph E. Schwarz, Ronen Spiegel, Daniel Tibussek, Enza Maria Valente, Eugen Boltshauser
Published 2012Artigo -
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SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome by Natalie D. Shaw, Harrison Brand, Zachary A Kupchinsky, Hemant Bengani, Lacey Plummer, Takako I. Jones, Serkan Erdin, Kathleen A. Williamson, Joe Rainger, Alexei Stortchevoi, Kaitlin E. Samocha, Benjamin Currall, Donncha S. Dunican, Ryan L. Collins, Jason R. Willer, Angela Lek, Monkol Lek, Malik Nassan, Shahrin Pereira, Tammy Kammin, Diane Lucente, Alexandra Silva, Catarina M. Seabra, Colby Chiang, Yu An, Morad Ansari, Jacqueline K. Rainger, Shelagh Joss, Jill Smith, Margaret Lippincott, Sylvia Singh, Nirav Patel, Jenny W Jing, Jennifer Law, Nalton Ferraro, Alain Verloès, Anita Rauch, Katharina Steindl, Markus Zweier, Ianina Scheer, Daisuke Sato, Nobuhiko Okamoto, Christina M. Jacobsen, Jeanie B. Tryggestad, Steven D. Chernausek, Lisa A. Schimmenti, Benjamin Brasseur, Claudia Cesaretti, José Elías García‐Ortíz, Tatiana Pineda Buitrago, Orlando Pérez Silva, Jodi D. Hoffman, W. Mühlbauer, Klaus W. Ruprecht, Bart Loeys, Masato Shino, Angela M. Kaindl, Chie Hee Cho, Cynthia C. Morton, Richard R. Meehan, Veronica van Heyningen, Eric C. Liao, Ravikumar Balasubramanian, Janet E. Hall, Stephanie B. Seminara, Daniel G. MacArthur, Steven A. Moore, Koh-ichiro Yoshiura, James F. Gusella, Joseph A. Marsh, John M. Graham, Angela E. Lin, Nicholas Katsanis, Peter L. Jones, William F. Crowley, Erica E. Davis, David Fitzpatrick, Michael E. Talkowski
Published 2017Artigo
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