6 Einträge gefunden

1. Homozygous HOXB1 loss-of-function mutation in a large family with hereditary congenital facial paresis

   1. Vogel, Markus
   2. Velleuer, Eunike
   3. Schmidt-Jiménez, Leon F
   4. Mayatepek, Ertan
   5. Borkhardt, Arndt
   6. Alawi, Malik
   7. Kutsche, Kerstin

   2016 - Forschungsinformationssystem des UKE
2. Establishment of the first newborn screening program in the People's Democratic Republic of Laos.

   1. Hoehn, Thomas
   2. Lukacs, Zoltan
   3. Stehn, Maren
   4. Mayatepek, Ertan
   5. Philavanh, Kedsatha
   6. Bounnack, Saysanasongkham

   2013 - Forschungsinformationssystem des UKE
3. Chronic pancreatitis in branched-chain organic acidurias--a case of methylmalonic aciduria and an overview of the literature.

   1. Marquard, Jan
   2. Tarik, El Scheich
   3. Klee, Dirk
   4. Schmitt, Marcus
   5. Meissner, Thomas
   6. Mayatepek, Ertan
   7. Oh, Jun

   2011 - Forschungsinformationssystem des UKE
4. Liver fibrosis in recessive multicystic kidney diseases: transient elastography for early detection.

   1. Kummer, Sebastian
   2. Sagir, Abdurrahman
   3. Pandey, Simone
   4. Feldkötter, Markus
   5. Habbig, Sandra
   6. Körber, Friederike
   7. Ney, Dietrich

   2011 - Forschungsinformationssystem des UKE
5. Therapy-refractory gastrointestinal motility disorder in a child with c-kit mutations.

   1. Breuer, Christian
   2. Oh, Jun
   3. Molderings, Gerhard-J
   4. Schemann, Michael
   5. Kuch, Birgit
   6. Mayatepek, Ertan
   7. Adam, Rüdiger

   2010 - Forschungsinformationssystem des UKE
6. Urinary alpha-ketoglutarate is elevated in patients with hyperinsulinism-hyperammonemia syndrome.

   1. Meissner, Thomas
   2. Mayatepek, Ertan
   3. Kinner, Martina
   4. Santer, René

   2004 - Forschungsinformationssystem des UKE