5 Einträge gefunden

1. Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy

   1. Hofhuis, Julia
   2. Bersch, Kristina
   3. Büssenschütt, Ronja
   4. Drzymalski, Marzena
   5. Liebetanz, David
   6. Nikolaev, Viacheslav O
   7. Wagner, Stefan

   2017 - Forschungsinformationssystem des UKE
2. Microduplication of 3p26.3 in nonsyndromic intellectual disability indicates an important role of CHL1 for normal cognitive function

   1. Shoukier, Moneef
   2. Fuchs, Sigrid
   3. Schwaibold, Eva
   4. Lingen, Michael
   5. Gärtner, Jutta
   6. Brockmann, Knut
   7. Zirn, Birgit

   2013 - Forschungsinformationssystem des UKE
3. Choroid plexus transcytosis and exosome shuttling deliver folate into brain parenchyma

   1. Grapp, Marcel
   2. Wrede, Arne
   3. Schweizer, Michaela
   4. Hüwel, Sabine
   5. Galla, Hans-Joachim
   6. Snaidero, Nicolas
   7. Simons, Mikael

   2013 - Forschungsinformationssystem des UKE - frei zugänglich
4. Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults

   1. Kohlschütter, Alfried
   2. Bley, Annette
   3. Brockmann, Knut
   4. Gärtner, Jutta
   5. Krägeloh-Mann, Ingeborg
   6. Rolfs, Arndt
   7. Schöls, Ludger

   2010 - Forschungsinformationssystem des UKE
5. Early reduction of total N-acetyl-aspartate-compounds in patients with classical vanishing white matter disease. A long-term follow-up MRS study.

   1. Dreha-Kulaczewski, Steffi F
   2. Dechent, Peter
   3. Finsterbusch, Jürgen
   4. Brockmann, Knut
   5. Gärtner, Jutta
   6. Frahm, Jens
   7. Hanefeld, Folker A

   2008 - Forschungsinformationssystem des UKE