4 Einträge gefunden

1. The mutation p.D313Y is associated with organ manifestation in Fabry disease

   1. du Moulin, M
   2. Koehn, A F
   3. Golsari, A
   4. Dulz, S
   5. Atiskova, Y
   6. Patten, M
   7. Münch, J

   2017 - Forschungsinformationssystem des UKE
2. Decreased plasma concentration of von Willebrand factor antigen (VWF:Ag) in patients with glycogen storage disease type Ia

   1. Mühlhausen, C
   2. Schneppenheim, R
   3. Budde, U
   4. Merkel, M
   5. Muschol, N
   6. Ullrich, K
   7. Santer, R

   2005 - Forschungsinformationssystem des UKE
3. Severe phenotype despite high residual glutaryl-CoA dehydrogenase activity: a novel mutation in a Turkish patient with glutaric aciduria type I.

   1. Mühlhausen, C
   2. Christensen, E
   3. Schwartz, M
   4. Muschol, N
   5. Ullrich, K
   6. Lukacs, Z

   2003 - Forschungsinformationssystem des UKE
4. Infantile cobalamin deficiency with cerebral lactate accumulation and sustained choline depletion.

   1. Horstmann, Martin
   2. Neumaier-Probst, E
   3. Lukacs, Z
   4. Steinfeld, R
   5. Ullrich, K
   6. Kohlschütter, A

   2003 - Forschungsinformationssystem des UKE