Výsledky vyhledávání - Adolphs, Nicolai

Role of distraction osteogenesis in craniomaxillofacial surgery Autor Ernst, Nicole, Adolphs, Nicolai

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RapidSplint: virtual splint generation for orthognathic surgery – results of a pilot series Autor Adolphs, Nicolai, Liu, Weichen, Keeve, Erwin, Hoffmeister, Bodo

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Contemporary Correction of Dentofacial Anomalies: A Clinical Assessment Autor Adolphs, Nicolai, Ernst, Nicole, Keeve, Erwin, Hoffmeister, Bodo

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Transpalatal distraction for the management of maxillary constriction in pediatric patients Autor Adolphs, Nicolai, Ernst, Nicole, Hoffmeister, Bodo, Raguse, Jan-Dirk

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Distraction Osteogenesis After Stem Cell Transplantation: A Pioneer Approach Autor Voss, Jan Oliver, Kühl, Jörg-Sven, Holm, Maike, Hauptmann, Kathrin, Adolphs, Nicolai

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Mutation c.943G>T (p.Ala315Ser) in FGFR2 Causing a Mild Phenotype of Crouzon Craniofacial Dysostosis in a Three-Generation Family Autor Graul-Neumann, Luitgard M., Klopocki, Eva, Adolphs, Nicolai, Mensah, Martin A., Kress, Wolfram

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Penetrating Foreign Bodies in Head and Neck Trauma: A Surgical Challenge Autor Voss, Jan Oliver, Thieme, Nadine, Doll, Christian, Hartwig, Stefan, Adolphs, Nicolai, Heiland, Max, Raguse, Jan-Dirk

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Clinical outcome after orbital floor fracture reduction with special regard to patient's satisfaction Autor Hartwig, Stefan, Nissen, Marie-Christine, Voss, Jan Oliver, Doll, Christian, Adolphs, Nicolai, Heiland, Max, Raguse, Jan Dirk

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De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction Autor Ehmke, Nadja, Graul-Neumann, Luitgard, Smorag, Lukasz, Koenig, Rainer, Segebrecht, Lara, Magoulas, Pilar, Scaglia, Fernando, Kilic, Esra, Hennig, Anna F., Adolphs, Nicolai, Saha, Namrata, Fauler, Beatrix, Kalscheuer, Vera M., Hennig, Friederike, Altmüller, Janine, Netzer, Christian, Thiele, Holger, Nürnberg, Peter, Yigit, Gökhan, Jäger, Marten, Hecht, Jochen, Krüger, Ulrike, Mielke, Thorsten, Krawitz, Peter M., Horn, Denise, Schuelke, Markus, Mundlos, Stefan, Bacino, Carlos A., Bonnen, Penelope E., Wollnik, Bernd, Fischer-Zirnsak, Björn, Kornak, Uwe

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Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency Autor Krone, Nils, Reisch, Nicole, Idkowiak, Jan, Dhir, Vivek, Ivison, Hannah E., Hughes, Beverly A., Rose, Ian T., O'Neil, Donna M., Vijzelaar, Raymon, Smith, Matthew J., MacDonald, Fiona, Cole, Trevor R., Adolphs, Nicolai, Barton, John S., Blair, Edward M., Braddock, Stephen R., Collins, Felicity, Cragun, Deborah L., Dattani, Mehul T., Day, Ruth, Dougan, Shelley, Feist, Miriam, Gottschalk, Michael E., Gregory, John W., Haim, Michaela, Harrison, Rachel, Haskins Olney, Ann, Hauffa, Berthold P., Hindmarsh, Peter C., Hopkin, Robert J., Jira, Petr E., Kempers, Marlies, Kerstens, Michiel N., Khalifa, Mohamed M., Köhler, Birgit, Maiter, Dominique, Nielsen, Shelly, O'Riordan, Stephen M., Roth, Christian L., Shane, Kate P., Silink, Martin, Stikkelbroeck, Nike M. M. L., Sweeney, Elizabeth, Szarras-Czapnik, Maria, Waterson, John R., Williamson, Lori, Hartmann, Michaela F., Taylor, Norman F., Wudy, Stefan A., Malunowicz, Ewa M., Shackleton, Cedric H. L., Arlt, Wiebke

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