5 Einträge gefunden

1. Long-term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening

   1. Mütze, Ulrike
   2. Garbade, Sven F
   3. Gleich, Florian
   4. Lindner, Martin
   5. Freisinger, Peter
   6. Hennermann, Julia B
   7. Thimm, Eva

   2023 - Forschungsinformationssystem des UKE - frei zugänglich
2. Neonatal screening for isovaleric aciduria:Reducing the increasingly high false-positive rate in Germany

   1. Murko, Simona
   2. Aseman, Asra Dadkhah
   3. Reinhardt, Friederike
   4. Gramer, Gwendolyn
   5. Okun, Jürgen Günther
   6. Mütze, Ulrike
   7. Santer, René

   2023 - Forschungsinformationssystem des UKE - frei zugänglich
3. Maternal Vitamin B12 Deficiency Detected by Newborn Screening-Evaluation of Causes and Characteristics

   1. Reischl-Hajiabadi, Anna T
   2. Garbade, Sven F
   3. Feyh, Patrik
   4. Weiss, Karl Heinz
   5. Mütze, Ulrike
   6. Kölker, Stefan
   7. Hoffmann, Georg F

   2022 - Forschungsinformationssystem des UKE - frei zugänglich
4. Newborn screening and disease variants predict neurological outcome in isovaleric aciduria

   1. Mütze, Ulrike
   2. Henze, Lucy
   3. Gleich, Florian
   4. Lindner, Martin
   5. Grünert, Sarah C
   6. Spiekerkoetter, Ute
   7. Santer, René

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
5. Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy

   1. Syrbe, Steffen
   2. Harms, Frederike L
   3. Parrini, Elena
   4. Montomoli, Martino
   5. Mütze, Ulrike
   6. Helbig, Katherine L
   7. Polster, Tilman

   2017 - Forschungsinformationssystem des UKE