Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Margret Heddrich‐Ellerbrok"'
Autor:
Júlio César Rocha, Heather Bausell, Amaya Bélanger-Quintana, Laurie Bernstein, Hülya Gökmen-Özel, Alexandra Jung, Anita MacDonald, Fran Rohr, Esther van Dam, Margret Heddrich-Ellerbrok
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 28, Iss , Pp 100771- (2021)
Background: The metabolic dietitian/nutritionist (hereafter ‘dietitian’) plays an essential role in the nutritional management of patients with phenylketonuria (PKU), including those on pegvaliase. Currently, more educational support and clinical
Externí odkaz:
https://doaj.org/article/7da1310c6578481e9e90c62904657daa
Autor:
Karina Grohmann‐Held, Peter Burgard, Christoph G. O. Baerwald, Skadi Beblo, Stephan vom Dahl, Anibh Das, Katharina Dokoupil, Sandra Fleissner, Peter Freisinger, Margret Heddrich‐Ellerbrok, Alexandra Jung, Vanessa Korpel, Johannes Krämer, Dinah Lier, Esther M. Maier, Uta Meyer, Chris Mühlhausen, Martha Newger, Ulrike Och, Ursula Plöckinger, Stefanie Rosenbaum‐Fabian, Frank Rutsch, René Santer, Petra Schick, Martin Schwarz, Ute Spiekerkötter, Ursula Strittmatter, Alena G. Thiele, Athanasia Ziagaki, Ulrike Mütze, Florian Gleich, Sven F. Garbade, Stefan Kölker
Publikováno v:
Journal of inherited metabolic diseaseREFERENCES. 45(6)
To prevent maternal phenylketonuria (PKU) syndrome low phenylalanine concentrations (target range, 120-360 μmol/L) during pregnancy are recommended for women with PKU. We evaluated the feasibility and effectiveness of current recommendations and ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d73c92a48559927d2d1c35868aad7268
https://pubmed.ncbi.nlm.nih.gov/36054426
https://pubmed.ncbi.nlm.nih.gov/36054426
Autor:
Martin Schwarz, Julia B. Hennermann, Stephan vom Dahl, Annemarie Klimek, Ursula Plöckinger, Frank Rutsch, Margret Heddrich-Ellerbrok, F Lang, Klaus Schöne, Markus Ott, Klaus G Parhofer, Christoph Baerwald
Publikováno v:
Annals of Nutrition and Metabolism. 76:251-258
Background: Only few data on dietary management of adult phenylketonuria (PKU) patients are published. Objectives: This study aimed to assess living situation, dietary practices, and health conditions of early-treated adult PKU patients. Methods: A t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::852231ae3a07cc63aac22023656ad221
https://doi.org/10.1159/000510260
https://doi.org/10.1159/000510260
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::668eb34e15bb299b6fa18cc6ad57511d
https://doi.org/10.3390/nu13010134
https://doi.org/10.3390/nu13010134