11 Einträge gefunden

1. Impact of interventional and non-interventional variables on anthropometric long-term development in glutaric aciduria type 1: A national prospective multi-centre study

   1. Märtner, E M Charlotte
   2. Maier, Esther M
   3. Mengler, Katharina
   4. Thimm, Eva
   5. Schiergens, Katharina A
   6. Marquardt, Thorsten
   7. Santer, René

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
2. Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision

   1. Boy, Nikolas
   2. Mühlhausen, Chris
   3. Maier, Esther M
   4. Heringer, Jana
   5. Assmann, Birgit
   6. Burgard, Peter
   7. Dixon, Marjorie

   2017 - Forschungsinformationssystem des UKE
3. The domain-specific and temperature-dependent protein misfolding phenotype of variant medium-chain acyl-CoA dehydrogenase

   1. Jank, Johanna M
   2. Maier, Esther M
   3. Reiβ, Dunja D
   4. Haslbeck, Martin
   5. Kemter, Kristina F
   6. Truger, Marietta S
   7. Sommerhoff, Christian P

   2014 - Forschungsinformationssystem des UKE - frei zugänglich
4. Low lysine diet in glutaric aciduria type I--effect on anthropometric and biochemical follow-up parameters.

   1. Boy, Nikolas
   2. Haege, Gisela
   3. Heringer, Jana
   4. Assmann, Birgit
   5. Mühlhausen, Chris
   6. Ensenauer, Regina
   7. Maier, Esther M

   2013 - Forschungsinformationssystem des UKE
5. What are effects of a spaced activation of virtual patients in a pediatric course?

   1. Maier, Esther M
   2. Hege, Inga
   3. Muntau, Ania C
   4. Huber, Johanna
   5. Fischer, Martin R

   2013 - Forschungsinformationssystem des UKE - frei zugänglich
6. Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I - A decade of experience.

   1. Kölker, Stefan
   2. Boy, S P Nikolas
   3. Heringer, Jana
   4. Müller, Edith
   5. Maier, Esther M
   6. Ensenauer, Regina
   7. Mühlhausen, Chris

   2012 - Forschungsinformationssystem des UKE
7. Use of guidelines improves the neurological outcome in glutaric aciduria type I.

   1. Heringer, Jana
   2. Boy, S P Nikolas
   3. Ensenauer, Regina
   4. Assmann, Birgit
   5. Zschocke, Johannes
   6. Harting, Inga
   7. Lücke, Thomas

   2010 - Forschungsinformationssystem des UKE
8. Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I.

   1. Harting, Inga
   2. Neumaier-Probst, Eva
   3. Seitz, Angelika
   4. Maier, Esther M
   5. Assmann, Birgit
   6. Baric, Ivo
   7. Troncoso, Monica

   2009 - Forschungsinformationssystem des UKE
9. 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
10. Disease manifestations and X inactivation in heterozygous females with Fabry disease.

    1. Maier, Esther M
    2. Osterrieder, Stephanie
    3. Whybra, Catharina
    4. Ries, Markus
    5. Gal, Andreas
    6. Beck, Michael
    7. Roscher, Adelbert A

    2006 - Forschungsinformationssystem des UKE
11. Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessment.

    1. Stadler, Sonja C
    2. Polanetz, Roman
    3. Maier, Esther M
    4. Heidenreich, Sylvia C
    5. Niederer, Birgit
    6. Mayerhofer, Peter U
    7. Lagler, Florian

    2006 - Forschungsinformationssystem des UKE