6 Einträge gefunden

1. The spectrum of peripheral neuropathy in disorders of the mitochondrial trifunctional protein

   1. Grünert, Sarah C
   2. Eckenweiler, Matthias
   3. Haas, Dorothea
   4. Lindner, Martin
   5. Tsiakas, Konstantinos
   6. Santer, René
   7. Tucci, Sara

   2021 - Forschungsinformationssystem des UKE
2. Phenotype in an Infant with SOD1 Homozygous Truncating Mutation

   1. Andersen, Peter M
   2. Nordström, Ulrika
   3. Tsiakas, Konstantinos
   4. Johannsen, Jessika
   5. Volk, Alexander E
   6. Bierhals, Tatjana
   7. Zetterström, Per

   2019 - Forschungsinformationssystem des UKE
3. Group 3 medulloblastoma in a patient with a GYS2 germline mutation and glycogen storage disease 0a

   1. Holsten, Till
   2. Tsiakas, Konstantinos
   3. Kordes, Uwe
   4. Bison, Brigitte
   5. Pietsch, Torsten
   6. Rutkowski, Stefan
   7. Santer, René

   2018 - Forschungsinformationssystem des UKE
4. LYRM7 - associated complex III deficiency: A clinical, molecular genetic, MR tomographic, and biochemical study

   1. Hempel, Maja
   2. Kremer, Laura S
   3. Tsiakas, Konstantinos
   4. Alhaddad, Bader
   5. Haack, Tobias B
   6. Löbel, Ulrike
   7. Feichtinger, René G

   2017 - Forschungsinformationssystem des UKE
5. Nectin-4 Mutations Causing Ectodermal Dysplasia with Syndactyly Perturb the Rac1 Pathway and the Kinetics of Adherens Junction Formation

   1. Fortugno, Paola
   2. Josselin, Emmanuelle
   3. Tsiakas, Konstantinos
   4. Agolini, Emanuele
   5. Cestra, Gianluca
   6. Teson, Massimo
   7. Santer, René

   2014 - Forschungsinformationssystem des UKE
6. Long-term outcomes after liver transplantation for deoxyguanosine kinase deficiency: a single-center experience and a review of the literature

   1. Grabhorn, Enke
   2. Tsiakas, Konstantinos
   3. Herden, Uta
   4. Fischer, Lutz
   5. Freisinger, Peter
   6. Marquardt, Thorsten
   7. Ganschow, Rainer

   2014 - Forschungsinformationssystem des UKE