Haege, Gisela Dipl.-Psych., Dipl.-Wirtschaftsinf.Universität HeidelbergHeidelberg
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Co-Autoren (Uni Heidelberg)
- Lindner, Martin (5)
- Glahn, Esther M. (4)
- Hörster, Friederike (3)
- Staufner, Christian (3)
- Haas, Dorothea (2)
- Riderer, Alina (2)
- Langhans, Claus-Dieter (2)
- Fang-Hoffmann, Junmin (2)
- Müller, Edith (2)
- Zwickler, Tamaris (2)
- Kool, Marcel (1)
- Völcker, Hans Eberhard (1)
- Jamiolkowski, Dagmar (1)
- Krastel, Hermann (1)
- Assmann, Birgit (1)
- Förl, Birgit (1)
- Weimer, Petra (1)
- Schuhmann, Vera (1)
- Rupp, Kathrin (1)
- Hinderhofer, Katrin (1)
- Harting, Inga (1)
- Okun, Jürgen G. (1)
- Mackensen, Friederike (1974-2016) (1)
- Springer, Christina (1)
- Garbade, Sven (1)
- Bartram, Claus R. (1)
Co-Autoren (extern)
- Zeman, Jiri (1)
- Garcia‐Cazorla, Angels (1)
- Trefz, Friedrich K. (1)
- Schwab, Karl O. (1)
- Mühlhausen, Chris (1)
- Maier, Esther M. (1)
- Ensenauer, Regina (1)
- Leichsenring, Michael (1)
- Lücke, Thomas (1)
- Tacke, Uta (1)
- Wendel, Udo (1)
Publikationen in heiBIB
- Workshop for Pediatric Research <52., 2016, Frankfurt am Main>: Abstracts of the 52nd Workshop for Pediatric Research : Frankfurt, Germany. 27-28 October 2016 / Rhea van den Bruck, Patrick P. Weil, Thomas Ziegenhals, Philipp Schreiner, Stefan Juranek, Daniel Gö… , 10 May 2017. - 9 S.
In: Molecular and Cellular Pediatrics, ISSN 2194-7791. 4(2017), Suppl. 1, Artikel-ID 5, Seite 1-9
DOI: 10.1186/s40348-017-0071-0
- Gramer, Gwendolyn: Long-chain polyunsaturated fatty acid status in children, adolescents and adults with phenylketonuria / Gwendolyn Gramer, Gisela Haege, Claus-Dieter Langhans, Vera Schuhmann, Peter Burgard, Georg F. Hoffm… , 18 April 2016. - 6 S.
In: Prostaglandins, leukotrienes and essential fatty acids, ISSN 1532-2823. 109(2016), Seite 52-57
DOI: 10.1016/j.plefa.2016.04.005
- Boy, Nikolas: A cross-sectional controlled developmental study of neuropsychological functions in patients with glutaric aciduria type I / Nikolas Boy, Jana Heringer, Gisela Haege, Esther M. Glahn, Georg F. Hoffmann, Sven F. Garbade, Stefa… . -
London: BioMed Central, 22 December 2015. - 1 Online-Ressource (12 Seiten)
DOI: 10.1186/s13023-015-0379-6
- Gramer, Gwendolyn: Medium-chain Acyl-CoA dehydrogenase deficiency : evaluation of genotype-phenotype correlation in patients detected by newborn screening / Gwendolyn Gramer, Gisela Haege, Junmin Fang-Hoffmann, Georg F. Hoffmann, Claus R. Bartram, Katrin Hi… , 05 May 2015. - 12 S.
In: JIMD reports, ISSN 2192-8312. 23(2015), Seite 101-112
DOI: 10.1007/8904_2015_439
- Burgard, Peter: Neonatal mortality and outcome at the end of the first year of life in early onset urea cycle disorders—review and meta-analysis of observational studies published over more than 35 years / Peter Burgard, Stefan Kölker, Gisela Haege, Martin Lindner, Georg F. Hoffmann, 2016. - 11 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 39(2016), 2, Seite 219-229
DOI: 10.1007/s10545-015-9901-1
- Jamiolkowski, Dagmar: Behavioural and emotional problems, intellectual impairment and health-related quality of life in patients with organic acidurias and urea cycle disorders / Dagmar Jamiolkowski, Stefan Kölker, Esther M. Glahn, Ivo Barić, Jiri Zeman, Matthias R. Baumgartner,… , [2016]. - 11 S. : Diagramme
In: Journal of inherited metabolic disease, ISSN 1573-2665. 39(2016), 2, Seite 231-241
DOI: 10.1007/s10545-015-9887-8
- Kölker, Stefan: Erratum to: The phenotypic spectrum of organic acidurias and urea cycle disorders : part 2 : the evolving clinical phenotype / Stefan Kölker, Vassili Valayannopoulos, Alberto B. Burlina, Jolanta Sykut-Cegielska, Frits A. Wijbur… , November 2015. - 2 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 38(2015), 6, Seite 1157-1158
DOI: 10.1007/s10545-015-9868-y
- Kölker, Stefan: Erratum to: The phenotypic spectrum of organic acidurias and urea cycle disorders : part 1 : the initial presentation / Stefan Kölker, Angeles Garcia Cazorla, Vassili Valayannopoulos, Allan M. Lund, Alberto B. Burlina, J… , November 2015. - 2 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 38(2015), 6, Seite 1155-1156
DOI: 10.1007/s10545-015-9867-z
- Kölker, Stefan: The phenotypic spectrum of organic acidurias and urea cycle disorders : part 2 : the evolving clinical phenotype / Stefan Kölker, Vassili Valayannopoulos, Alberto B. Burlina, Jolanta Sykut-Cegielska, Frits A. Wijbur… , November 2015. - 16 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 38(2015), 6, Seite 1059-1074
DOI: 10.1007/s10545-015-9840-x
- Kölker, Stefan: The phenotypic spectrum of organic acidurias and urea cycle disorders : part 1: the initial presentation / Stefan Kölker, Angeles Garcia Cazorla, Vassili Valayannopoulos, Allan M. Lund, Alberto B. Burlina, J… , November 2015. - 17 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 38(2015), 6, Seite 1041-1057
DOI: 10.1007/s10545-015-9839-3
- Boy, Nikolas: A cross-sectional controlled developmental study of neuropsychological functions in patients with glutaric aciduria type I / Nikolas Boy, Jana Heringer, Gisela Haege, Esther M. Glahn, Georg F. Hoffmann, Sven F. Garbade, Stefa… , 22 December 2015
In: Orphanet journal of rare diseases, ISSN 1750-1172. 10(2015) Artikel-Nr. 163, 12 S.
DOI: 10.1186/s13023-015-0379-6
- Haas, Dorothea: Diagnosis and therapeutic monitoring of inborn errors of creatine metabolism and transport using liquid chromatography-tandem mass spectrometry in urine, plasma and CSF / Dorothea Haas, Hongying Gan-Schreier, Claus-Dieter Langhans, Alexandros Anninos, Gisela Haege, Peter… . - 7 S.
In: Gene, ISSN 1879-0038. 538(2014), 1, S. 188-194
DOI: 10.1016/j.gene.2014.01.019
- Zwickler, Tamaris: Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemia / Zwickler, T. ; Riderer, A. ; Haege, G. ; Hoffmann, G. F. ; Kolker, S. ; Burgard, P.. - 7 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 37(2014), 1, S. 31-37
DOI: 10.1007/s10545-013-9621-3
- Haas, Dorothea: Prenatal presentation and diagnostic evaluation of suspected Smith-Lemli-Opitz (RSH) syndrome / Dorothea Haas, Gisela Haege, Georg F. Hoffmann, and Peter Burgard, 26 March 2013. - 4 S.
In: American journal of medical genetics, ISSN 1552-4833. 161(2013), 5, Seite 1008-1011
DOI: 10.1002/ajmg.a.35837
- Gramer, Gwendolyn: Living with an inborn error of metabolism detected by newborn screening—Parents’ perspectives on child development and impact on family life / Gwendolyn Gramer, Gisela Haege, Esther M. Glahn, Georg F. Hoffmann, Martin Lindner, Peter Burgard, 2014. - 7 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 37(2014), 2, Seite 189-195
DOI: 10.1007/s10545-013-9639-6
- Gramer, Gwendolyn: Visual functions in phenylketonuria : evaluating the dopamine and long-chain polyunsaturated fatty acids depletion hypotheses / Gwendolyn Gramer, Birgit Förl, Christina Springer, Petra Weimer, Gisela Haege, Friederike Mackensen,… , January 2013. - 7 S.
In: Molecular genetics and metabolism, ISSN 1096-7206. 108(2013), 1, Seite 1-7
DOI: 10.1016/j.ymgme.2012.10.021
- Kölker, Stefan: Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I : a decade of experience / Stefan Kölker, S. P. Nikolas Boy, Jana Heringer, Edith Müller, Esther M. Maier, Regina Ensenauer, Ch… , 2012. - 9 S.
In: Molecular genetics and metabolism, ISSN 1096-7206. 107(2012), 1, Seite 72-80
DOI: 10.1016/j.ymgme.2012.03.021
- Zwickler, Tamaris: Metabolic decompensation in methylmalonic aciduria : which biochemical parameters are discriminative? / Tamaris Zwickler, Gisela Haege, Alina Riderer, Friederike Hörster, Georg F. Hoffmann, Peter Burgard,… . - 10 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 35(2012), 5, S. 797-806
DOI: 10.1007/s10545-011-9426-1
- Burgard, Peter: Newborn screening programmes in Europe : arguments and efforts regarding harmonization : Part 2 - From screening laboratory results to treatment, follow-up and quality assurance / Peter Burgard, Kathrin Rupp, Martin Lindner, Gisela Haege, Tessel Rigter, Stephanie S. Weinreich, J.… . - 13 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 35(2012), 4, S. 613-625
DOI: 10.1007/s10545-012-9484-z
- Boy, Nikolas: Low lysine diet in glutaric aciduria type I - effect on anthropometric and biochemical follow-up parameters / Nikolas Boy, Gisela Haege, Jana Heringer, Birgit Assmann, Chris Mühlhausen, Regina Ensenauer, Esther… , 2013. - 9 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 36(2013), 3, Seite 525-533
DOI: 10.1007/s10545-012-9517-7
- Lindner, Martin: Efficacy and outcome of expanded newborn screening for metabolic diseases : report of 10 years from South-West Germany / Martin Lindner, Gwendolyn Gramer, Gisela Haege, Junmin Fang-Hoffmann, Karl O. Schwab, Uta Tacke, Fri… , 2011. - 10 S.
In: Orphanet journal of rare diseases, ISSN 1750-1172. 6(2011), Artikel-ID 44, Seite 1-10
DOI: 10.1186/1750-1172-6-44
- Heringer-Seifert, Jana: Use of guidelines improves the neurological outcome in glutaric aciduria type I / Jana Heringer, S. P. Nikolas Boy, Regina Ensenauer, Birgit Assmann, Johannes Zschocke, Inga Harting,… , [November 2010]. - 10 S. : Illustrationen
In: Annals of neurology, ISSN 1531-8249. 68(2010), 5 vom: Nov., Seite 743-752
DOI: 10.1002/ana.22095
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