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. German newborn screening for Cystic fibrosis:Parental perspectives and suggestions for improvements

   1. Gapp, Simon
   2. Garbade, Sven F
   3. Feyh, Patrik
   4. Brockow, Inken
   5. Nennstiel, Uta
   6. Hoffmann, Georg F
   7. Sommerburg, Olaf

   2023 - Forschungsinformationssystem des UKE - frei zugänglich
3. Combined Newborn Screening Allows Comprehensive Identification also of Attenuated Phenotypes for Methylmalonic Acidurias and Homocystinuria

   1. Schnabel, Elena
   2. Kölker, Stefan
   3. Gleich, Florian
   4. Feyh, Patrik
   5. Hörster, Friederike
   6. Haas, Dorothea
   7. Fang-Hoffmann, Junmin

   2023 - Forschungsinformationssystem des UKE - frei zugänglich
4. 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
5. Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany.

   1. Kölker, Stefan
   2. Garbade, Sven F
   3. Boy, Nikolas
   4. Maier, Esther M
   5. Meissner, Thomas
   6. Mühlhausen, Chris
   7. Hennermann, Julia B

   2007 - Forschungsinformationssystem des UKE