检索结果 - Adolphs, Nicolai

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

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

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

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

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Distraction Osteogenesis After Stem Cell Transplantation: A Pioneer Approach 由 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 由 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 由 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 由 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 由 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 由 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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