Resultados da busca - Adolphs, Nicolai

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

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

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

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

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