Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Agnes van Teeffelen-Heithoff"'
Autor:
Margret Heddrich-Ellerbrok, Vanessa Korpel, Carmen Rohde, Anibh M. Das, Katharina Dokoupil, Dinah Lier, Dorothea Möslinger, Stephan vom Dahl, Aleksandra Fischer, U. Meyer, Friederike Bärhold, Skadi Beblo, Eva Thimm, Sebene Mayorandan, Stefanie Rosenbaum-Fabian, Agnes van Teeffelen-Heithoff, Janina Lahl, Anne-Kathrin Neugebauer, Anna Fekete, Nina Bogovic, Monika Jörg-Streller, Michel Hochuli, Peter Freisinger, Ulrike Och
Publikováno v:
Nutrients
Nutrients, Vol 13, Iss 134, p 134 (2021)
Volume 13
Issue 1
Nutrients, Vol 13, Iss 134, p 134 (2021)
Volume 13
Issue 1
Background: Tyrosinaemia type 1 is a rare inherited metabolic disease caused by an enzyme defect in the tyrosine degradation pathway. It is treated using nitisinone and a low-protein diet. In a workshop in 2013, a group of nutritional specialists fro
Autor:
Eva Wolfgart, Thorsten Marquardt, Sarah Leuders, Reinhold Feldmann, J. Weglage, Frank Rutsch, Agnes van Teeffelen-Heithoff, Torsten Ott, Lydia Vogelpohl, Ulrike Och, Marcel du Moulin
Publikováno v:
JIMD reports. 13
Identifying phenylalanine hydroxylase (PAH) mutations associated with sapropterin response in phenylketonuria (PKU) would be an advantageous means to determine clinical benefit to sapropterin therapy.Sapropterin response, defined as a ≥30 % reducti
Autor:
Michael J. Lentze, Thomas Reinehr, Mathilde Kersting, Agnes van Teeffelen-Heithoff, Kurt Widhalm
Adipositas, Diabetes mellitus, Allergien – welche Ernährung ist die richtige? Ernährungsbedingte Krankheiten nehmen rasant zu, insbesondere bei Kindern und Jugendlichen. Die Ernährungsmedizin spielt daher in der Prävention, aber auch in der The
Autor:
Reinhold Feldmann, Jonas Denecke, Agnes van Teeffelen-Heithoff, D. Gödde, H. G. Koch, Thorsten Marquardt, Josef Weglage, M. Grenzebach
Publikováno v:
Journal of inherited metabolic disease. 25(4)
In a group of 87 consecutive patients with hyperphenylalaninaemia born since 1990, only 3 patients showed a (temporary) decrease of serum phenylalanine levels after tetrahydrobiopterin (BH4) loading in usual doses (20 mg/kg body weight).
Autor:
G. Koch, Thorsten Marquardt, Josef Weglage, C. Oberwittler, Agnes van Teeffelen-Heithoff, H. Gerding, J. Schellscheidt
Publikováno v:
Journal of Inherited Metabolic Disease. 23:83-84
Autor:
Josef Weglage, Hans Georg Koch, Birgit Fünders, M Pietsch, Kurt Ullrich, Agnes van Teeffelen-Heithoff
Publikováno v:
Pediatric Research. 36:44A-44A
The intellectual outcome of patients with HPA (serum phe levels under free diet < 600 μmol/l) was not systematically studied so far. Therefore we tested 31 patients (age: 22 ± 4 years) for IQ (WAIS-R) and school performance. In addition cranial MRI