Role of distraction osteogenesis in craniomaxillofacial surgery

par Ernst, Nicole, Adolphs, Nicolai
Publié dans Innov Surg Sci (2016)

RapidSplint: virtual splint generation for orthognathic surgery – results of a pilot series

par Adolphs, Nicolai, Liu, Weichen, Keeve, Erwin, Hoffmeister, Bodo
Publié 2014

Contemporary Correction of Dentofacial Anomalies: A Clinical Assessment

par Adolphs, Nicolai, Ernst, Nicole, Keeve, Erwin, Hoffmeister, Bodo
Publié dans Dent J (Basel) (2016)

Transpalatal distraction for the management of maxillary constriction in pediatric patients

par Adolphs, Nicolai, Ernst, Nicole, Hoffmeister, Bodo, Raguse, Jan-Dirk
Publié dans Ann Maxillofac Surg (2015)

Distraction Osteogenesis After Stem Cell Transplantation: A Pioneer Approach

par Voss, Jan Oliver, Kühl, Jörg-Sven, Holm, Maike, Hauptmann, Kathrin, Adolphs, Nicolai
Publié dans Ann Maxillofac Surg (2018)

Mutation c.943G>T (p.Ala315Ser) in FGFR2 Causing a Mild Phenotype of Crouzon Craniofacial Dysostosis in a Three-Generation Family

par Graul-Neumann, Luitgard M., Klopocki, Eva, Adolphs, Nicolai, Mensah, Martin A., Kress, Wolfram
Publié dans Mol Syndromol (2017)

Penetrating Foreign Bodies in Head and Neck Trauma: A Surgical Challenge

par Voss, Jan Oliver, Thieme, Nadine, Doll, Christian, Hartwig, Stefan, Adolphs, Nicolai, Heiland, Max, Raguse, Jan-Dirk
Publié dans Craniomaxillofac Trauma Reconstr (2018)

Clinical outcome after orbital floor fracture reduction with special regard to patient's satisfaction

par Hartwig, Stefan, Nissen, Marie-Christine, Voss, Jan Oliver, Doll, Christian, Adolphs, Nicolai, Heiland, Max, Raguse, Jan Dirk
Publié dans Chin J Traumatol (2019)

De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction

par 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
Publié dans Am J Hum Genet (2017)

Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency

par 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
Publié 2012