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Multidisciplinary long‐term care and modern surgical treatment of congenital melanocytic nevi – recommendations by the CMN surgery network.
Published in:
Journal der Deutschen Dermatologischen Gesellschaft, 2019, v. 17, n. 10, p. 1005, doi. 10.1111/ddg.13951
By:
- Ott, Hagen;
- Krengel, Sven;
- Beck, Otfrid;
- Böhler, Kornelia;
- Böttcher‐Haberzeth, Sophie;
- Cangir, Özlem;
- Fattouh, Miriam;
- Häberle, Beate;
- Hüging, Martina;
- Königs, Ingo;
- Kosch, Ferdinand;
- Rok, Kralj;
- Marathovouniotis, Nicos;
- Meyer, Lutz;
- Neuhaus, Kathrin;
- Rothe, Karin;
- Schiestl, Clemens;
- Sinnig, Mechthild;
- Theiler, Martin;
- Heydt, Susanne
Publication type:
Article
Multidisziplinäre Langzeitbetreuung und zeitgemäße chirurgische Therapie kongenitaler melanozytärer Nävi – Empfehlungen des Netzwerks Nävuschirurgie.
Published in:
Journal der Deutschen Dermatologischen Gesellschaft, 2019, v. 17, n. 10, p. 1005, doi. 10.1111/ddg.13951_g
By:
- Ott, Hagen;
- Krengel, Sven;
- Beck, Otfrid;
- Böhler, Kornelia;
- Böttcher‐Haberzeth, Sophie;
- Cangir, Özlem;
- Fattouh, Miriam;
- Häberle, Beate;
- Hüging, Martina;
- Königs, Ingo;
- Kosch, Ferdinand;
- Rok, Kralj;
- Marathovouniotis, Nicos;
- Meyer, Lutz;
- Neuhaus, Kathrin;
- Rothe, Karin;
- Schiestl, Clemens;
- Sinnig, Mechthild;
- Theiler, Martin;
- der Heydt, Susanne
Publication type:
Article
Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
Published in:
Birth Defects Research, 2017, v. 109, p. 1063, doi. 10.1002/bdr2.1042
By:
- Zhang, Rong;
- Marsch, Florian;
- Kause, Franziska;
- Degenhardt, Franziska;
- Schmiedeke, Eeberhard;
- Märzheuser, Stefanie;
- Hoppe, Bernd;
- Bachour, Haitham;
- Boemers, Thomas M.;
- Schäfer, Matthias;
- Spychalski, Nicole;
- Neser, Jörg;
- Leonhardt, Johannes;
- Kosch, Ferdinand;
- Ure, Benno;
- Gómez, Barbara;
- Lacher, Martin;
- Deffaa, Oliver J.;
- Palta, Markus;
- Wittekindt, Boris
Publication type:
Article
Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
Published in:
Birth Defects Research, 2017, v. 109, n. 13, p. 1063, doi. 10.1002/bdr2.1042
By:
- Zhang, Rong;
- Marsch, Florian;
- Kause, Franziska;
- Degenhardt, Franziska;
- Schmiedeke, Eeberhard;
- Märzheuser, Stefanie;
- Hoppe, Bernd;
- Bachour, Haitham;
- Boemers, Thomas M.;
- Schäfer, Matthias;
- Spychalski, Nicole;
- Neser, Jörg;
- Leonhardt, Johannes;
- Kosch, Ferdinand;
- Ure, Benno;
- Gómez, Barbara;
- Lacher, Martin;
- Deffaa, Oliver J.;
- Palta, Markus;
- Wittekindt, Boris
Publication type:
Article
Re‐sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL‐like association, and isolated anorectal malformation.
Published in:
Birth Defects Research, 2022, v. 114, n. 10, p. 478, doi. 10.1002/bdr2.2008
By:
- Thiem, Corina E.;
- Stegmann, Jil D.;
- Hilger, Alina C.;
- Waffenschmidt, Lea;
- Bendixen, Charlotte;
- Köllges, Ricarda;
- Schmiedeke, Eberhard;
- Schäfer, Frank‐Mattias;
- Lacher, Martin;
- Kosch, Ferdinand;
- Grasshoff‐Derr, Sabine;
- Kabs, Carmen;
- Neser, Jörg;
- Jenetzky, Ekkehart;
- Fazaal, Julia;
- Schumacher, Johannes;
- Hoefele, Julia;
- Ludwig, Kerstin U.;
- Reutter, Heiko
Publication type:
Article

Found: 5

Multidisciplinary long‐term care and modern surgical treatment of congenital melanocytic nevi – recommendations by the CMN surgery network.

Multidisziplinäre Langzeitbetreuung und zeitgemäße chirurgische Therapie kongenitaler melanozytärer Nävi – Empfehlungen des Netzwerks Nävuschirurgie.

Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.

Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.

Re‐sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL‐like association, and isolated anorectal malformation.