6 Einträge gefunden

1. Dried blood spots in the diagnosis of lysosomal storage disorders--possibilities for newborn screening and high-risk population screening.

   1. Lukacs, Zoltan
   2. Nieves Cobos, Paulina Alexandra
   3. Keil, Angelika
   4. Hartung, R
   5. Mengel, E
   6. Beck, M
   7. Deschauer, M

   2011 - Forschungsinformationssystem des UKE
2. Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data

   1. Mehta, A
   2. Beck, M
   3. Elliott, P
   4. Giugliani, R
   5. Linhart, A
   6. Sunder-Plassmann, G
   7. Schiffmann, R

   2009 - Forschungsinformationssystem des UKE
3. Association between polymorphisms of endothelial nitric oxide synthase gene (NOS3) and left posterior wall thickness (LPWT) of the heart in Fabry disease.

   1. Rohard, Imke
   2. Schaefer, E
   3. Kampmann, C
   4. Beck, M
   5. Gal, Andreas

   2008 - Forschungsinformationssystem des UKE
4. Direct comparison of enzyme measurements from dried blood and leukocytes from male and female Fabry disease patients.

   1. Lukacs, Zoltan
   2. Hartung, R
   3. Beck, M
   4. Keil, A
   5. Mengel, E

   2007 - Forschungsinformationssystem des UKE
5. Cumulative incidence rates of the mucopolysaccharidoses in Germany.

   1. Baehner, F
   2. Schmiedeskamp, C
   3. Krummenauer, F
   4. Miebach, E
   5. Bajbouj, M
   6. Whybra, C
   7. Kohlschütter, Alfried

   2005 - Forschungsinformationssystem des UKE
6. The ratio of alpha-galactosidase to beta-glucuronidase activities in dried blood for the identification of female Fabry disease patients.

   1. Lukacs, Z
   2. Keil, A
   3. Kohlschütter, Alfried
   4. Beck, M
   5. Mengel, E

   2005 - Forschungsinformationssystem des UKE