Haege G - Search Results

1

Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2. From screening laboratory results to treatment, follow-up and quality assurance.

Burgard P, Rupp K, Lindner M, Haege G, Rigter T, Weinreich SS, Loeber JG, Taruscio D, Vittozzi L, Cornel MC, Hoffmann GF. Burgard P, et al. Among authors: haege g. J Inherit Metab Dis. 2012 Jul;35(4):613-25. doi: 10.1007/s10545-012-9484-z. Epub 2012 Apr 28. J Inherit Metab Dis. 2012. PMID: 22544437

2

Living with an inborn error of metabolism detected by newborn screening-parents' perspectives on child development and impact on family life.

Gramer G, Haege G, Glahn EM, Hoffmann GF, Lindner M, Burgard P. Gramer G, et al. Among authors: haege g. J Inherit Metab Dis. 2014 Mar;37(2):189-95. doi: 10.1007/s10545-013-9639-6. Epub 2013 Aug 16. J Inherit Metab Dis. 2014. PMID: 23949009

3

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.

Burgard P, Kölker S, Haege G, Lindner M, Hoffmann GF. Burgard P, et al. Among authors: haege g. J Inherit Metab Dis. 2016 Mar;39(2):219-29. doi: 10.1007/s10545-015-9901-1. Epub 2015 Dec 3. J Inherit Metab Dis. 2016. PMID: 26634836

4

Efficacy and outcome of expanded newborn screening for metabolic diseases--report of 10 years from South-West Germany.

Lindner M, Gramer G, Haege G, Fang-Hoffmann J, Schwab KO, Tacke U, Trefz FK, Mengel E, Wendel U, Leichsenring M, Burgard P, Hoffmann GF. Lindner M, et al. Among authors: haege g. Orphanet J Rare Dis. 2011 Jun 20;6:44. doi: 10.1186/1750-1172-6-44. Orphanet J Rare Dis. 2011. PMID: 21689452 Free PMC article.

5

Metabolic decompensation in methylmalonic aciduria: which biochemical parameters are discriminative?

Zwickler T, Haege G, Riderer A, Hörster F, Hoffmann GF, Burgard P, Kölker S. Zwickler T, et al. Among authors: haege g. J Inherit Metab Dis. 2012 Sep;35(5):797-806. doi: 10.1007/s10545-011-9426-1. Epub 2012 Jan 17. J Inherit Metab Dis. 2012. PMID: 22249333

6

Low lysine diet in glutaric aciduria type I--effect on anthropometric and biochemical follow-up parameters.

Boy N, Haege G, Heringer J, Assmann B, Mühlhausen C, Ensenauer R, Maier EM, Lücke T, Hoffmann GF, Müller E, Burgard P, Kölker S. Boy N, et al. Among authors: haege g. J Inherit Metab Dis. 2013 May;36(3):525-33. doi: 10.1007/s10545-012-9517-7. Epub 2012 Sep 13. J Inherit Metab Dis. 2013. PMID: 22971958 Clinical Trial.

7

The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype.

Kölker S, Valayannopoulos V, Burlina AB, Sykut-Cegielska J, Wijburg FA, Teles EL, Zeman J, Dionisi-Vici C, Barić I, Karall D, Arnoux JB, Avram P, Baumgartner MR, Blasco-Alonso J, Boy SP, Rasmussen MB, Burgard P, Chabrol B, Chakrapani A, Chapman K, Cortès I Saladelafont E, Couce ML, de Meirleir L, Dobbelaere D, Furlan F, Gleich F, González MJ, Gradowska W, Grünewald S, Honzik T, Hörster F, Ioannou H, Jalan A, Häberle J, Haege G, Langereis E, de Lonlay P, Martinelli D, Matsumoto S, Mühlhausen C, Murphy E, de Baulny HO, Ortez C, Pedrón CC, Pintos-Morell G, Pena-Quintana L, Ramadža DP, Rodrigues E, Scholl-Bürgi S, Sokal E, Summar ML, Thompson N, Vara R, Pinera IV, Walter JH, Williams M, Lund AM, Garcia-Cazorla A. Kölker S, et al. Among authors: haege g. J Inherit Metab Dis. 2015 Nov;38(6):1059-74. doi: 10.1007/s10545-015-9840-x. Epub 2015 Apr 15. J Inherit Metab Dis. 2015. PMID: 25875216

8

Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn Screening.

Gramer G, Haege G, Fang-Hoffmann J, Hoffmann GF, Bartram CR, Hinderhofer K, Burgard P, Lindner M. Gramer G, et al. Among authors: haege g. JIMD Rep. 2015;23:101-12. doi: 10.1007/8904_2015_439. Epub 2015 May 5. JIMD Rep. 2015. PMID: 25940036 Free PMC article.

9

Behavioural and emotional problems, intellectual impairment and health-related quality of life in patients with organic acidurias and urea cycle disorders.

Jamiolkowski D, Kölker S, Glahn EM, Barić I, Zeman J, Baumgartner MR, Mühlhausen C, Garcia-Cazorla A, Gleich F, Haege G, Burgard P; E-IMD consortium. Jamiolkowski D, et al. Among authors: haege g. J Inherit Metab Dis. 2016 Mar;39(2):231-41. doi: 10.1007/s10545-015-9887-8. Epub 2015 Aug 27. J Inherit Metab Dis. 2016. PMID: 26310964

10

A cross-sectional controlled developmental study of neuropsychological functions in patients with glutaric aciduria type I.

Boy N, Heringer J, Haege G, Glahn EM, Hoffmann GF, Garbade SF, Kölker S, Burgard P. Boy N, et al. Among authors: haege g. Orphanet J Rare Dis. 2015 Dec 22;10:163. doi: 10.1186/s13023-015-0379-6. Orphanet J Rare Dis. 2015. PMID: 26693825 Free PMC article.

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